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# EUCROF

The European CRO Federation

## Sitemaps

- [XML Sitemap](https://eucrof.eu/sitemap.xml): Contains all public & indexable URLs for this website.

## Posts

- [News Summary](https://eucrof.eu/blog/)
- [21 July 2026 - Audit Readiness for CRAs](https://eucrof.eu/21-july-2026-audit-readiness-for-cras/) - Webinar Date & Time 21 July 2026 from 11:00 AM to 12:30 PM (CEST) Webinar Overview This presentation provides an overview of audit readiness principles tailored for Clinical Research Associates (CRAs) and their managers (administrative and operational). It focuses on equipping CRAs with the knowledge and practical tools needed to prepare for and successfully navigate
- [EUCROF Welcomes Four New Members to its Executive Board](https://eucrof.eu/eucrof-welcomes-four-new-members-to-its-executive-board/) - EUCROF Welcomes Four New Members to its Executive Board Sofia, Bulgaria, 5 June 2026 - During the EUCROF General Assembly held in Sofia, Bulgaria, members elected four new professionals to join the EUCROF Executive Board, further strengthening the federation's expertise, diversity of perspectives, and commitment to advancing clinical research across Europe.The newly elected Board members
- [17 June 2026 - GCP Inspection](https://eucrof.eu/17-june-2026-gcp-inspection/) - Webinar Date & Time 17 June 2026 from 11:00 AM to 12:30 PM (CEST) Webinar Overview The presentation will cover trends in site level GCP inspection findings from major health authorities and provide insights on the compliance to ICH GCP E6 R3 guidelines. In addition, I am hoping to deep dive into some proactive initiatives
- [20 May 2026 - Celebrating Clinical Trials Day: Clinical Research Through the Ages](https://eucrof.eu/20-may-2026-celebrating-clinical-trials-day-clinical-research-through-the-ages/) - Webinar Date & Time 20 May 2026 from 11:00 AM to 12:00 PM (CEST) Webinar Overview The webinar will begin with an introduction to EUCROF, including an overview of our activities, experience, and track record in supporting and advancing clinical research across Europe. This will be followed by a lecture exploring the evolution of clinical
- [EUCROF GDPR Code of Conduct Enters into Force Following CNIL Approval of Supervisory Body](https://eucrof.eu/eucrof-gdpr-code-of-conduct-enters-into-force-following-cnil-approval-of-supervisory-body/) - The French Data Protection Authority has formally accredited the EUCROF Supervisory Committee (COSUP), completing the final step needed to activate the first transnational GDPR Code of Conduct in the field of health across all 27 EU Member States. The European CRO Federation (EUCROF) is pleased to announce a landmark development for data protection in clinical
- [21 April 2026 - The ICH GCP R3 Roadmap: The Challenge of Vendor Management](https://eucrof.eu/21-april-2026-the-ich-gcp-r3-roadmap-the-challenge-of-vendor-management/) - Webinar Date & Time 21 April 2026 from 11:00 AM to 12:30 PM (CEST) Webinar Overview ICH E6(R3) introduces a new mindset for oversight of service providers, emphasizing proportionate risk management and systems-based quality rather than procedural compliance. These changes profoundly affect how sponsors – but also CROs - select, qualify, and monitor service providers
- [18 March 2026 - The ICH GCP R3 Roadmap: Risks management and R3](https://eucrof.eu/18-march-2026-the-ich-gcp-r3-roadmap-risks-management-and-r3/) - Webinar Date & Time 18 March 2026 from 03:00 PM to 04:30 PM (CET) Webinar Overview ICH GCP is changing — and so is the meaning of “risk management.”With ICH GCP R3, regulators are no longer interested in perfect paperwork. They are interested in clear thinking, proportional controls, and real protection of patients and data.
- [25 February 2026 - MDR, IVDR, and the AI Act: What They Mean for Software as a Medical Device](https://eucrof.eu/25-february-2026-mdr-ivdr-and-the-ai-act-what-they-mean-for-software-as-a-medical-device/) - Webinar Date & Time 25 February 2026 from 04:00 PM to 05:30 PM (CET) Webinar Overview In this webinar, we will begin with an expert-led overview of the current MDR landscape, presented by the Medical Device Working Group.The regulatory landscape for medical devices (MDs) and in vitro diagnostics (IVDs) devices in Europe has undergone significant
- [21 January 2026 - Insights for Clinical Trial Sponsors: Navigating IVDR 2017/746 and CTR 536/2014](https://eucrof.eu/21-january-2026-insights-for-clinical-trial-sponsors-navigating-ivdr-2017-746-and-ctr-536-2014/) - Webinar Date & Time 21 January 2026 from 04:00 PM to 05:30 PM (CET) Webinar Overview As the regulatory landscape for clinical trials continues to evolve, sponsors must adapt to the complex requirements introduced by the In Vitro Diagnostic Regulation (IVDR 2017/746) and the Clinical Trials Regulation (CTR 536/2014). This presentation provides a practical overview
- [10 November 2025 - Free Webinar - EUCROF xShare Open Call 2025: Enabling Interoperable Health Data Sharing Across Europe](https://eucrof.eu/10-november-2025-webinar-eucrof-xshare-open-call-2025-enabling-interoperable-health-data-sharing-across-europe/) - Webinar Date & Time 10 November 2025 from 04:00 PM to 05:30 PM (CET) Webinar Overview EUCROF invites you to its second free xShare webinar, dedicated to the EUCROF xShare Open Call 2025. The xShare project, funded by Horizon Europe, aims to enable seamless health data sharing across Europe through the European Health Data Space
- [26 November 2025 - Unlocking the EU Market: Cost-Effective Strategies for Regulatory & Clinical Success](https://eucrof.eu/26-november-2025-unlocking-the-eu-market-cost-effective-strategies-for-regulatory-clinical-success/) - Webinar Date & Time 26 November 2025 from 03:00 PM to 04:30 PM (CET) Webinar Overview An exclusive session on how to design efficient clinical trials through careful budget planning and regulatory guidance for optimal resource allocation, incorporating both strategic designs and tactical monitoring approaches. 🔍 You will learn how to: ✅ Engage with EMA early: Use ITF,
- [12 November 2025 - From Awareness to Enrollment: Can Social Media Close the Gap in Patient Recruitment?](https://eucrof.eu/12-november-2025-from-awareness-to-enrollment-can-social-media-close-the-gap-in-patient-recruitment/) - Webinar Date & Time 12 November 2025 from 04:00 PM to 05:30 PM (CET) Webinar Overview Finding and engaging the right patients for clinical trials remains one of the industry’s greatest challenges—particularly when those patients are underdiagnosed, underrepresented, or unaware that their symptoms may qualify them for participation. In many therapeutic areas, from women’s health
- [The Launch of IMPACT (Improving and Acting for a Stronger European Clinical Trials Environment)](https://eucrof.eu/the-launch-of-impact-improving-and-acting-for-a-stronger-european-clinical-trials-environment/) - In July 2025, EUCROF launched its newest initiative, IMPACT (Improving and Acting for a Stronger European Clinical Trials Environment) One of the first activities is the Mapping of National Initiatives to Enhance the Clinical Trials Environment in Europe. EUCROF is presenting key initiatives from France, Germany, Spain, Italy, Netherlands, Poland, Chech Republic, Slovakia, Sweden and
- [8 July 2025 - IMPACT – Improving and Acting for a Stronger European Clinical Trials Environment](https://eucrof.eu/8-july-2025-impact-improving-and-acting-for-a-stronger-european-clinical-trials-environment/) - Mapping National Initiatives to Boost Clinical Trials Across Europe Webinar Date & Time 8 July from 04:00 PM to 05:30 PM (CEST) The webinar is for free. Webinar Overview Join us for the launch of IMPACT – a major new initiative from EUCROF designed to reinvigorate the clinical trial landscape in Europe. With Europe experiencing
- [25 September 2025 - Electronic Signatures in Clinical Trials](https://eucrof.eu/25-september-2025-electronic-signatures-in-clinical-trials/) - Webinar Date & Time 25 September 2025 from 11:00 AM to 12:30 PM (CEST) Webinar Overview With the pandemic it became apparent that we use electronic signatures on documents very often. Staff had to stay at home and the home office was even a requirement in some countries. Printing, signing, scanning, mailing the documents for
- [10 September 2025 - ICH GCP E6(R3): What CRAs Need to Know](https://eucrof.eu/10-september-2025-ich-gcp-e6r3-what-cras-need-to-know/) - Webinar Date & Time 10 September 2025 from 04:00 PM to 05:30 PM (CEST) Webinar Overview The International Council for Harmonisation (ICH) released a revision of its Good Clinical Practice guideline—E6(R3). This update introduces changes with a strong focus on quality by design, critical thinking, and risk-based approaches throughout the clinical trial lifecycle. This webinar
- [15 July 2025 - Clinical Trials in Armenia, Uzbekistan and Ukraine](https://eucrof.eu/15-july-2025-clinical-trials-in-armenia-uzbekistan-and-ukraine/) - This webinar will explore the recruitment advantages of conducting clinical trials in Armenia, Uzbekistan, and Ukraine. We will discuss the region's cost-effectiveness, streamlined regulatory processes, and access to diverse patient populations.
- [International Clinical Trial Day 2025](https://eucrof.eu/international-clinical-trial-day-2025/) - EUCROF celebrates Clinical Trials Day… A moment to honour the power of clinical research to transform lives, extend hope, and advance scientific research… EUCROF would like to recognise the thousands of professionals, CROs, and partners who turn protocols into progress across Europe and beyond. We are honoured to represent those who lead the way in
- [17 June 2025 - The ICH GCP R3 Roadmap: Changes and Challenges of ICH E6 (R3) - Are you ready?](https://eucrof.eu/17-june-2025-the-ich-gcp-r3-roadmap-changes-and-challenges-of-ich-e6-r3-are-you-ready/) - In the EU, the ICH Guideline E6 (R3) will be effective on 23 July 2025. The guideline underwent a major restructuring and modernisation. The risk-based and risk-proportionate approach has been introduced into every aspect of a clinical trial and modern techniques like the use of computerized systems (e.g., eCRF, eTMF, eConsent), as well as remote Source Data Verification are now included in the Guideline. Data Governance plays an important role, not only for sponsors but also for investigators.
- [14 May 2025 - Navigating the Clinical Hiring Landscape in 2025](https://eucrof.eu/14-may-2025-navigating-the-clinical-hiring-landscape-in-2025/) - The CRO industry is experiencing a period of volatility, shaped by mergers, acquisitions, and the ongoing push for innovation. While AI-driven platforms and DCTs are transforming the landscape
- [EUCROF Code of Conduct for Service Providers in Clinical Research](https://eucrof.eu/eucrof-code-of-conduct-for-service-providers-in-clinical-research/) - Call for candidates for the Governance Body:The Supervisory Committee (COSUP) Dear EUCROF Members, As you may already be aware, the EUCROF Code of Conduct is the first transnational GDPR code in the health sector. Approved by the supervisory authorities of all 27 EU Member States, it provides the specific interpretation of how the GDPR should
- [28/01/25 - EUCROF Announces New Executive Board for 2024–2026](https://eucrof.eu/28-01-25-eucrof-announces-new-executive-board-for-2024-2026/) - EUCROF Announces New Executive Board for 2024–2026 We are delighted to announce the election of the new Executive Board of the European CRO Federation (EUCROF), which took place in December 2024. This board will serve a two-year term, leading EUCROF in its continued mission to promote high-quality clinical research across Europe and beyond. The newly elected
- [30/06 - EUCROF Podcast #5 - "History of Clinical Trials"](https://eucrof.eu/30-06-eucrof-podcast-5-history-of-clinical-trials/) - The EUCROF Events & Training working group is happy to share with all of you the 5th EUCROF podcast: "History of Clinical Trials" prepared by Dr. Goran Vesov, MD as member of the EUCROF Events & Training WG. What is this podcast all about? Tune in to the EUCROF Podcast on the History of Clinical Trials, to
- [10/07 - EUCROF Podcast n. 1 "Risk Based and Remote Monitoring"](https://eucrof.eu/10-07-eucrof-podcast-n-1-risk-based-and-remote-monitoring/) - The EUCROF Events & Training working group is happy to share with all of you the first EUCROF podcast: "Risk Based and Remote Monitoring" prepared by Goran Vesov and Ana Stojkovic as members of the EUCROF Events & Training WG, who held a successful webinar for EUCROF in July 2019 and they comment on the developments of
- [10/08 - EUCROF Podcast n. 2 "Validation of Computerized Systems in GCP Environment"](https://eucrof.eu/10-08-eucrof-podcast-n-2-validation-of-computerized-systems-in-gcp-environment/) - EUCROF is excited to post the second Podcast on the topic: "Validation of Computerized Systems in GCP Environment​" Hear from two experts Simone Bucerius, member of the EUCROF Events & Training Working Group, and her colleague at FGK Clinical Research GmbH, Guenter Woelfl, about all key aspects of validation of computerized systems which has become
- [03/09 - EUCROF Podcast n. 3 - "eConsent"](https://eucrof.eu/03-09-eucrof-podcast-n-3-econsent/) - EUCROF is very pleased to post its third Podcast on the topic: "eConsent​" How will eConsent transform your clinical trial? Tune in to the EUCROF Podcast on eConsent, and explore stakeholder perspectives on how eConsent transforms clinical trials from our guest speakers. Find out about the trial participant experience with eConsent, the preservation of participant-site
- [19/11 - EUCROF Podcast #4 - "EU CTR and CTIS. Ready or not… here it comes!"](https://eucrof.eu/19-11-eucrof-podcast-4-eu-ctr-and-ctis-ready-or-not-here-it-comes/) - The EUCROF Events & Training working group is happy to share with all of you the fourth EUCROF podcast: "EU CTR and CTIS. Ready or not… here it comes!" prepared by Marieke Meulemans as member of the EUCROF Events & Training WG, who held a successful webinar for EUCROF in April 2021 titled “EMA Clinical Trials Information
- [31/10/23 – Meet the EUCROF Talent Engagement Task Force!](https://eucrof.eu/31-10-23-meet-the-eucrof-talent-engagement-task-force/) - The EUCROF Talent Engagement Task Force introduces itself: Let us meet the Task Force and discover what are its activities and goals!
- [2-3/03 - Patient Partnering in Clinical Development. How to Best Integrate Patients into your Strategies and Operations in Clinical Development](https://eucrof.eu/2-3-03-patient-partnering-in-clinical-development-how-to-best-integrate-patients-into-your-strategies-and-operations-in-clinical-development/) - Patient Partnering in Clinical Development How to Best Integrate Patients into your Strategies and Operations in Clinical Development Berlin (Germany), 2 - 3 March 2020 EUCROF President, Dr Martine Dehlinger-Kremer, was invited to present at the “Patient Partnering in Clinical Development - How to Best Integrate Patients into your Strategies and Operations in Clinical Development”
- [13/03 - CORONAVIRUS and Clinical Trials - Advice requested from EMA](https://eucrof.eu/13-03-coronavirus-and-clinical-trials-advice-requested-from-ema/) - CORONAVIRUS and Clinical Trials - Advice requested from EMA 13 March 2020 In respect to the Coronavirus and the performance of clinical trials, on Friday 13 March 2020, EUCROF has asked the EMA for advice on how to best behave so that clinical trials are not endangered to be considered as GCP non-compliant. See below the letter submitted to
- [20/03 - Guidance on the Management of Clinical Trials during the COVID-19 (Coronavirus) pandemic](https://eucrof.eu/20-03-guidance-on-the-management-of-clinical-trials-during-the-covid-19-coronavirus-pandemic/) - Guidance on the Management of Clinical Trials during the COVID-19 (Coronavirus) pandemic 20 March 2020 Please find below the links to the Guidance on the Management of Clinical Trials during the COVID-19 (Coronavirus) pandemic and the related press release published today in the EMA website. Guidance: https://ec.europa.eu/health/sites/health/files/files/eudralex/vol-10/guidanceclinicaltrials_covid19_en.pdf
- [20/05 - HACRO: Digital campaign to raise clinical trial awareness](https://eucrof.eu/20-05-hacro-digital-campaign-to-raise-clinical-trial-awareness/) - HACRO: Digital campaign to raise clinical trial awareness 20 May 2020 #work together #shape the future #enjoy life! This was the key message of the Digital Campaign organized by the Hellenic Association of CROs (HACRO) on the occasion of the International Clinical Trials Day on 20 May 2020. “Our experience with COVID-19 was particularly important for
- [18/06 - Use of Televisits in Studies and Related PV Concerns](https://eucrof.eu/18-06-use-of-televisits-in-studies-and-related-pv-concerns/) - APPLIED CLINICAL TRIALS Article written by the EUCROF PharmacoVigilance WG and published on 18 June 2020. Use of Televisits in Studies and Related PV Concerns by Xavier Fournie, MD, Zurab Koberidze, Nicolas Tsiakkas, Marco Anelli, MD The COVID-19 pandemic has triggered a surge of attention and tremendous increase of use of televisits (also called tele-consultation
- [08/09 - Brexit: new Regulatory Rules in the UK as of 1 January 2021](https://eucrof.eu/08-09-brexit-new-regulatory-rules-in-the-uk-as-of-1-january-2021/) - The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) issued a dozen documents explaining how medicines licensure will work after the Brexit transition period expires on 1 January 2021.
- [20/11 - Annual Clinical Trials Symposium](https://eucrof.eu/20-11-annual-clinical-trials-symposium/) - This year, the Annual Clinical Trials Symposium “2020: A YEAR OF UNPRECEDENTED CHALLENGES IN CLINICAL RESEARCH”, under the patronage of EUCROF, will take place from Romania as a virtual conference. Dr Martine Dehlinger-Kremer, President of EUCROF, is going to hold the welcome speech of the Conference and will moderate the Session on “Latest Updates Related
- [01/12 - Internship in EUCROF Affiliates](https://eucrof.eu/01-12-internship-in-eucrof-affiliates/) - Dear EUCROF Affiliates, As you might know, my University (Università del Piemonte Orientale, Novara, Italy), together with the Universitad Miguel Hernandez (Spain), the Université de Namur (Belgium), the Université de Liege (Belgium), and Humboldt Universität (Germany), are running a European Master financed by the European Union that concentrates on research and development of drugs and cosmetics. While
- [03/12 - Annual Duchenne Patient Academy Conference](https://eucrof.eu/03-12-annual-duchenne-patient-academy-conference/) - On 03 December 2020, EUCROF President, Dr Martine Dehlinger-Kremer, is going to attend the Annual Duchenne Patient Academy Conference, taking place from 30 November to 06 December 2020. This year it is a virtual event. 39 patient organizations will participate, 52 countries will be represented. Over 200 participants were expected. Dr Dehlinger-Kremer will present on “What
- [07/12 - Executive Board re-elected at EUCROF's Fall General Assembly!](https://eucrof.eu/07-12-executive-board-re-elected-at-eucrofs-fall-general-assembly/) - Last week EUCROF held its Fall General Assembly for 2020. Due to the continued travel restrictions associated to the ongoing COVID-19 pandemic, the GA was held remotely on 3rd and 4th December. It was attended by over 40 participants, which was the highest number ever for such a meeting! The GA marked the end of
- [26/01 - The Current Status of European Research Related to COVID-19: The EUCROF Perspective](https://eucrof.eu/26-01-the-current-status-of-european-research-related-to-covid-19-the-eucrof-perspective/) - The Current Status of European Research Related to COVID-19:The EUCROF Perspective The unexpected SARS-CoV-2 impacted on all aspects of ordinary life especially when it comes to research activities. To face COVID-19 pandemic, many hospitals have been forced to drastically change their organisation in order to find as much space as possible to accommodate COVID-19 patients;
- [02/03 - Archiving Position Paper](https://eucrof.eu/02-03-archiving-position-paper/) - The archiving of clinical trial records is a required process that is in need of future direction to meet current business models as well as regulatory and legal expectations. A group of industry experts coalesced under EUCROF and the eClinical Forum to formulate a position paper discussing the needs and proposed practical directions for archiving
- [19/3 - eConsent Implementation Guide](https://eucrof.eu/19-3-econsent-implementation-guide/) - eConsent Implementation Guide The EUCROF and eClinical Forum Electronic Informed Consent (eConsent) Joint Task Force are pleased to announce the publication of the eConsent Implementation Guide (version 1). The joint task force was formed in 2019 with a view to look at some of the barriers to adoption of eConsent considering the benefits to stakeholders.
- [22/3 - GDPR : EUCROF Code of conduct officially submitted March 17th, 2021!](https://eucrof.eu/22-3-gdpr-eucrof-code-of-conduct-officially-submitted-march-17th-2021/) - Press Release 17 March 2021 The European CRO Federation (EUCROF), announces the submission for approval by the Data Protection Authorities of the 27 EU Member States and the European Data Protection Board, of its GDPR Code of Conduct for Service Providers in Clinical Research. CNIL (Commission Nationale de l'Informatique et des Libertés), the French Data
- [20/5 - International Clinical Trials Day](https://eucrof.eu/20-5-international-clinical-trials-day/) - International Clinical Trials Day 20 May 2021 The International Clinical Trials Day is set on 20th May as a celebration of James Lind’s very first clinical trial. Whilst working as a surgeon on a ship, Dr. James Lind (1716-1794) was appalled by the high mortality of scurvy amongst the sailors. He started the world’s first
- [28/5 - Partnering for Patients Conference](https://eucrof.eu/28-5-partnering-for-patients-conference/) - Partnering for Patients Conference 28 May 2021 On Friday 28 May 2021, the Greek Patients Association, the Hellenic Association of CROs (HACRO), the Pharma Innovation Forum Greece, the Hellenic Association of Pharmaceutical Companies (SFEE), the Panhellenic Union of Pharmaceutical Industry (PEF), together with the Association of Representatives of Pharmaceuticals & Specialties (SAFEE) are organising the
- [18/6 - 2022 European Conference on Clinical Research – Let's meet in Madrid!](https://eucrof.eu/18-6-2022-european-conference-on-clinical-research-lets-meet-in-madrid/) - 2022 European Conference on Clinical Research Let's meet in Madrid! EUCROF is pleased to invite you to browse through the link of the EUCROF Conference in Madrid, on 7 – 8 February 2022 6th European Conference on Clinical Research Join the 6th European Conference on Clinical Research to listen, discuss, exchange ideas on important topics Take
- [22/09 - EUCROF presented at EMA/GCP IWG workshop on AI in Clinical Research](https://eucrof.eu/22-09-eucrof-presented-at-ema-gcp-iwg-workshop-on-ai-in-clinical-research/) - "EUCROF presented at EMA/GCP IWG workshop on AI in Clinical Research" Fiona Maini represented EUCROF at a two day workshop with the EMA/GCP IWG on AI in Clinical Research. Fiona presented on Ethical and Trustworthy AI and the draft proposal on the new EU AI Act coming in. Fiona was invited to present given her
- [22/09 - EUCROF/eClinical Forum’s eConsent Implementation Guide - TOPRA Awards Finalist 2021](https://eucrof.eu/22-09-eucrof-eclinical-forums-econsent-implementation-guide-topra-awards-finalist-2021/) - "EUCROF/eClinical Forum’s eConsent Implementation Guide - TOPRA Awards Finalist 2021" The EUCROF and eClinical Forum Electronic Informed Consent (eConsent) Joint Task Force are pleased announce that the eConsent Implementation Guide they published earlier this year has been recognized by TOPRA and is a finalist at this year’s TOPRA Awards within the Innovation Category. The joint
- [24/09 - Artificial Intelligence (AI) in Pharmacovigilance: do we really need it…?](https://eucrof.eu/24-09-artificial-intelligence-ai-in-pharmacovigilance-do-we-really-need-it/) - "Artificial Intelligence (AI) in Pharmacovigilance: do we really need it…?" Part 1: The Technicalities “Artificial Intelligence” is one of the most used buzzwords in these days. However, there seems to be a lack of clarity about the meaning of terms such as “artificial intelligence (AI)”, “machine learning (ML)”, “data science (DS)” and “office automation (OA)”,
- [12/01 - EUCROF announces the launch of its electronic submission and approval platform for future adherents to the EUCROF GDPR Code of Conduct for Service Providers in Clinical Research (the EUCROF Code)](https://eucrof.eu/12-01-eucrof-announces-the-launch-of-its-electronic-submission-and-approval-platform-for-future-adherents-to-the-eucrof-gdpr-code-of-conduct-for-service-providers-in-clinical-research-the-eucrof-co/) - The European CRO Federation (EUCROF) announces the launch of its electronic submission and approval platform for future adherents to the EUCROF GDPR Code of Conduct for Service Providers in Clinical Research (the EUCROF Code). In March 2021, EUCROF announced the submission of its EUCROF Code to the CNIL (Commission Nationale de l'Informatique et des Libertés), the French Data
- [27/01 - Medical Device Regulation (MDR) - Useful Links](https://eucrof.eu/27-01-medical-device-regulation-mdr-useful-links/) - Medical Device Regulation (MDR) - Useful Links ​ • European Union (EU) Commission Website • Medical Device Coordination Group (MDCG) Guidance: This page provides a range of documents to assist stakeholders in applying Regulation (EU) 2017/745 on medical devices (MDR) and Regulation (EU) 2017/746 in vitro Diagnostic Medical Devices (IVDR) on in vitro diagnostic medical
- [7-8 Feb. 2022 - 6th European Conference on Clinical Research](https://eucrof.eu/7-8-feb-2022-6th-european-conference-on-clinical-research/) - 6th European Conference on Clinical Research ​ The 6th European Conference on Clinical Research took place on 07 & 08 February 2022 in Madrid (Spain) as a hybrid conference. In total there were 271 participants, 174 present in Madrid, with 97 joining on-line. The feedback of the conference has been very positive so far. Delegates appreciated
- [16 March 2022 - EUCROF President invited to the 20th Anniversary of ACRO](https://eucrof.eu/16-march-2022-eucrof-president-invited-to-the-20th-anniversary-of-acro/) - EUCROF President invited to the 20th Anniversary of ACRO ​ Our colleagues at the Association of Clinical Research Organizations (ACRO) celebrated their 20th anniversary on Wednesday, March 16th., 2022 and Dr Martine Dehlinger-Kremer, EUCROF President, was kindly invited and attended the event in Washington DC, representing EUCROF and its members. The event was attended by
- [9-10/6 - EUCROF Spring General Assembly, Prague (Czech Republic)](https://eucrof.eu/9-10-6-eucrof-spring-general-assembly-prague-czech-republic/) - The EUCROF Spring General Assembly took place in Prague (Czech Republic), on 9 and 10 June 2022. The meeting was held as a hybrid event, with 18 attendees in presence and 25 virtual participants, representing 18 countries. It was a great pleasure to finally meet in person many friends and colleagues, after the last General
- [14-15/06 – EUCROF attending the conect4children General Assembly in Ghent (Belgium)](https://eucrof.eu/14-15-06-eucrof-attending-the-conect4children-general-assembly-in-ghent-belgium/) - The EUCROF President, Dr Martine Dehlinger-Kremer was invited to attend the conect4children (c4c) General Assembly in Ghent (Belgium) on 14 and 15 June 2022. It was an excellent meeting. c4c, a collaborative network for Clinicals Trials for children, has progressed its activities as planned. Once fully established, c4c will be a key contributor to perform
- [28/06 – The article “EUCROF Benchmarking Project 2021” has been published on Läkemedelsmarknaden (Pharma Market).](https://eucrof.eu/28-06-the-article-eucrof-benchmarking-project-2021-has-been-published-on-lakemedelsmarknaden-pharma-market/) - We are very pleased to inform our readers that, at the end of the month of June, the article written by Jonny Sågänger “EUCROF Benchmarking Project 2021”, was published on the Swedish Journal Läkemedelsmarknaden (Pharma Market). The article was written thanks to the contribution of Dr Martine Dehlinger-Kremer (EUCROF President) and Benedikt van Nieuwenhove (President of
- [04/10 - EMA ACT EU DCT Workshop](https://eucrof.eu/04-10-ema-act-eu-dct-workshop/) - EMA ACT EU DCT Workshop ​ On October 4th, the EMA ACT EU DCT Workshop took place at EMA's headquarters in Amsterdam. This workshop was part of ACT EU (Accelerating Clinical Trials EU) - a joint initiative by the EC, HMA and the EMA, which aims at making the EU a more focal clinical trial location by
- [27/02/23 - The EU-X-CT Multi-stakeholder Initiative](https://eucrof.eu/27-02-23-the-eu-x-ct-multi-stakeholder-initiative/) - The EU-X-CT Multi-stakeholder Initiative ​ There is no EU legal framework that defines the conditions to access clinical trials in another EU country. To support patients, investigators and sponsors in enabling cross-border access to clinical trials, EFGCP and EFPIA have launched this initiative and representatives from patient organizations, industry, academia, CRO and medical society will
- [08/03/23 - Propositions on Remote Source Data Verification and Remote Source Data Review](https://eucrof.eu/08-03-23-propositions-on-remote-source-data-verification-and-remote-source-data-review/) - Propositions on Remote Source Data Verification and Remote Source Data Review A Proposition Paper from EUCROF’s rSDV/rSDR Task Force ​ The EUCROF rSDV/rSDR task force has released a newly updated version of the Propositions Paper for rSDV/rSDR (remote source data verification and review). The new version (March 2023) has been reviewed by external stakeholders and integrates
- [13/04/23 - Three white papers released by the Archiving and the Decommissioning Team](https://eucrof.eu/13-04-23-three-white-papers-released-by-the-archiving-and-the-decommissioning-team/) - Three White Papers released by the Archiving and the Decommissioning Team ​ EUCROF & the eClinical Forum Archiving and Decommission Team are pleased to announce the public release of three white papers: "Nature of a Distributed Trial Master File ‐ Practical Aspects" "The Decommissioning of Computerised Systems Used in Clinical Trials" "Data Formats Used in Clinical Trials"
- [13/05/23 – EUCROF Poster accepted at ISPOR 2023 (7-10 May 2023, Boston – USA)](https://eucrof.eu/13-05-23-eucrof-poster-accepted-at-ispor-2023-7-10-may-2023-boston-usa/) - EUCROF Poster accepted at ISPOR 2023 (7-10 May 2023, Boston – USA) Presentation of the Poster on “The Importance of Clinical Research Organizations (CRO) in Clinical Research and Impact of COVID-19 Pandemic”, at ISPOR 2023, on May 09th., 2023, Boston Conference & Exhibition Center, Boston, Massachusetts, USA. The goal of the project was to assess
- [31/07/23 – EUCROF Welcomes 2 New Members](https://eucrof.eu/31-07-23-eucrof-welcomes-2-new-members/) - EUCROF Welcomes 2 New Members (26 July 2023) EUCROF is particularly pleased to welcome two new contract research organisations to its membership - Evidenze (Portugal) joining EUCROF as an Associate Member and the Dow Institute of Biological, Biochemical & Pharmaceutical Sciences, Dow University of Health Sciences – IBBPS-DUHS (Pakistan) as a Partner. EUCROF members can
- [12/09/23 – EUCROF Paediatric Training](https://eucrof.eu/12-09-23-eucrof-paediatric-training/) - EUCROF Paediatric Training (12 September 2023 - Rome, Italy) On the 12th of September 2023, in Rome (Italy), in cooperation with the Ospedale Pediatrico Bambino Gesù, the EUCROF Paediatric Working Group organised the Training “Essentials of Paediatric Clinical Research - What you need to know when preparing, conducting and monitoring paediatric clinical trials” The aim was to
- [26/09/23 – EUCROF24 Conference: The Programme is out!](https://eucrof.eu/26-09-23-eucrof24-conference-the-programme-is-out/) - EUCROF24 Conference (19-20 February 2024) The Programme is out! Who is speaking at EUCROF24 and what subjects will be discussed...EUCROF is delighted to announce that the Conference Programme for EUCROF24 is now available.The programme is made up of presentations, expert panels and discussion groups reflecting the status of Clinical Research, whilst at the same time including views
- [01/10/23 –We have a new Glossary of technical terms (prepared by the EUCROF CTLogWG)](https://eucrof.eu/01-10-23-we-have-a-new-glossary-of-technical-terms-prepared-by-the-eucrof-ctlogwg/) - We have a new GLOSSARY of technical terms (prepared by the EUCROF Clinical Trials Logistics WG) The EUCROF recently-established Clinical Trial Logistics Working Group dynamically develops its activity. Mr. Martin King, one of the CTLogWG Members, launched the idea of putting together a glossary of technical terms, which was immediately approved by the other members. After
- [07/02/24 - Draft European Code of Conduct - PRESS RELEASE](https://eucrof.eu/07-02-24-draft-european-code-of-conduct-press-release/) - The European CRO Federation (EUCROF), announces its draft European Code of Conduct has passed a major milestone: the CNIL[1], in its plenary meeting held last January 25, has decided to submit the Code to the European Data Protection Board (EDPB). Last 25 January 2024, the CNIL notified EUCROF "… that the draft European Code of
- [17/06/24 - DIA2024 Global Annual Meeting - It is a first for EUCROF to be represented as a speaker!](https://eucrof.eu/17-06-24-dia2024-global-annual-meeting-it-is-a-first-for-eucrof-to-be-represented-as-a-speaker/) - Dr Martine Dehlinger-Kremer, EUCROF President, has been invited by Susan Lantis, Executive Director, Association of Clinical Research Professionals (ACRP), United States, to participate into the panel discussion: "A Clinical Research Workforce in Crisis: Imperatives for a Sustainable Staffing Model", taking place on Wednesday, 19 June at 1.15 PM PST. Dr Dehlinger-Kremer has been invited as President
- [25/09/24 - The EUCROF Code of Conduct has been approved!](https://eucrof.eu/25-09-24-the-eucrof-code-of-conduct-has-been-approved/) - Exciting News! The European CRO Federation (EUCROF) is proud to announce the official approval of the EUCROF Code for service providers in clinical research. This significant milestone is the result of extensive efforts by an international task force, organized under the New Technologies Working Group of EUCROF. The task force engaged in broad consultations with
- [15/12/24 - EUCROF Honorary Announcement - Chase and Marini became EUCROF Honorary Members](https://eucrof.eu/15-12-24-eucrof-honorary-announcement-chase-and-marini-became-eucrof-honorary-members/) - It is with immense pride and heartfelt enthusiasm that we officially announce the appointment of Dr Dagmar Chase and Dr Stefano Marini as EUCROF Honorary Members. This recognition was unanimously endorsed during the Fall General Assembly, held on December 5th, following the proposal of the Executive Board. The decision to confer this distinguished honour is a
- [25-26/01/24 - ACT EU Clinical Trials Analytics multi-stakeholder workshop.](https://eucrof.eu/25-26-01-24-act-eu-clinical-trials-analytics-multi-stakeholder-workshop/) - The European Medicines Agency has recently hosted a pivotal two-day workshop, focusing on the future of data analytics on clinical trials in the EU, under the ACT-EU initiative. The event, led by prominent figures including Peter Arlett, Lars Bo Nielsen, and Emer Cooke, centred on integrating data analytics into the clinical trial regulatory process. The
- [12/01/23 - EUCROF attending ACRP Workforce Development Global Roundtable - Post Session Summary](https://eucrof.eu/12-01-23-eucrof-attending-acrp-workforce-development-global-roundtable-post-session-summary/) - EUCROF attending ACRP Workforce Development Global Roundtable Post Session Summary ​ On January 12th, the Association of Clinical Research Professionals organised the ACRP’s Workforce Development Global Roundtable. This hybrid meeting connected industry stakeholders who share a deep interest in building the next generation of clinical research professionals and a diverse, research-ready workforce. The meeting objectives
- [10-11/02 - EUCROF Conference in Amsterdam (NL)](https://eucrof.eu/10-11-02-eucrof-conference-in-amsterdam-nl/) - What a memorable Conference! More than 320 delegates attended the 5th European Conference on Clinical Research organized by EUCROF on 10 - 11 February 2020 in Amsterdam, NL. Very high-level speakers, together with enthusiastic participants, discussed over two days the matter of “Science, Technology and Regulations Coming Together for Better Patients' Health”. With many side
- [Draft European Code of Conduct](https://eucrof.eu/draft-european-code-of-conduct/) - The European CRO Federation (EUCROF), announces its draft European Code of Conduct has passed a major milestone: the CNIL[1], in its plenary meeting held last January 25, has decided to submit the Code to the European Data Protection Board (EDPB). Last 25 January 2024, the CNIL notified EUCROF "… that the draft European Code of
- [EUCROF Spring General Assembly](https://eucrof.eu/eucrof-spring-general-assembly/) - The Spring General Assembly 2024, organized by the European CRO Federation – EUCROF, was held in Bucharest (Romania) on June 6 - 7, 2024. It brought together participants from all over Europe, and its Agenda covered many interesting topics, which led to engaging discussions. The social event and dinner at the Spring General Assembly 2024
- [DIA2024 Global Annual Meeting](https://eucrof.eu/say-salut-to-the-most-advanced-theme/) - It is a first for EUCROF to be represented as a speaker! Dr Martine Dehlinger-Kremer, EUCROF President, has been invited by Susan Lantis, Executive Director, Association of Clinical Research Professionals (ACRP), United States, to participate into the panel discussion: "A Clinical Research Workforce in Crisis: Imperatives for a Sustainable Staffing Model", taking place on Wednesday, 19
- [EUCROF response to EMA consultation on Draft Proposal for an Addendum on Transparency](https://eucrof.eu/eucrof-response-to-ema-consultation-on-draft-proposal-for-an-addendum-on-transparency/) - EUCROF responded to the EMA’s consultation on the 'Draft proposal for an addendum, on transparency, to the “Functional specifications for the EU portal and EU database to be audited' (EMA/42176/2014). On behalf of its members, EUCROF actively participates in the ongoing discussions and stakeholder meetings in relation to the implementation of the EU Clinical Trials Regulation.
- [Dr. Stefano Marini, invited speaker at the conference “The Annual Meeting of the Clinical Trials Community in Israel” (11/4)](https://eucrof.eu/dr-stefano-marini-invited-speaker-at-the-conference-the-annual-meeting-of-the-clinical-trials-community-in-israel-11-4/) - Dr. Stefano Marini, EUCROF President, is an invited speaker at the conference “The Annual Meeting of the Clinical Trials Community in Israel” taking place in Tel Aviv on April 11th. The title of his presentation is “Is it Still Worth Working for a CRO?” (http://bioforumconf.com/english-ctrials2016).
- [27/11 – GDPR Code of Conduct for Clinical Trials in progress](https://eucrof.eu/27-11-gdpr-code-of-conduct-for-clinical-trials-in-progress/) - EUCROF, the European CRO Federation, is the initiator of the first transnational "Code of Conduct", aimed at ensuring the compliance of clinical research service organisations (CROs) with the European General Data Protection Regulation (GDPR). For the success of this initiative, it is important to have the contribution of all stakeholders involved in clinical research programmes,
- [18-19/11 - EMA Regulatory Science to 2025](https://eucrof.eu/18-19-11-ema-regulatory-science-to-2025/) - LinkedIn On 18 & 19 November 2019, the European Medicines Agency convened stakeholders (including EUCROF, which was represented by its President, Dr Martine Dehlinger Kremer) for a workshop to discuss the outcome of the public consultation on the draft Regulatory Science Strategy to 2025, reflect on the prioritisation of core recommendations and identify concrete actions to
- [24/10 - Training on Essentials of Paediatric Clinical Research](https://eucrof.eu/24-10-training-on-essentials-of-paediatric-clinical-research/) - How preparing, conducting and monitoring paediatric clinical trials? These challenging questions were answered during the training “Essentials of Paediatric Clinical Research”, held in Madrid (Spain), on 24 October 2019. Over 50 participants coming from industry, clinical research organizations, academia and patient advocacy convened at C.N.I.O. (Centro Nacional de Investigaciones Oncológicas) in Madrid for this paediatric
- [16/10 - 1st Panhellenic Conference on Clinical Trial and Research (Greece)](https://eucrof.eu/16-10-1st-panhellenic-conference-on-clinical-trial-and-research-greece/) - 1st Panhellenic Conference on Clinical Trial and Research Athens, 16 October 2019 Dr Martine Dehlinger-Kremer, EUCROF President, was invited by the President, Mrs. Evangelia Koraki, and the Board of Directors of the Hellenic Association of CROs (HACRO) to attend the 1st Panhellenic Conference on Clinical Trial and Research. The conference, organized by the Association
- [11/10 - CLINICAL TRIALS SYMPOSIUM (Romania)](https://eucrof.eu/11-10-clinical-trials-symposium-romania/) - 11/10 - CLINICAL TRIALS SYMPOSIUM (Romania) This is a historical first ever event, organised in Romania under the patronage of the European CRO Federation (EUCROF) and of the Romanian Association of CROs (ACCSCR). The clinical research community of professionals in this region is of considerable expertise, and this improves clinical research across Europe. The CLINICAL
- [24/6 EUCROF – JCROA Meeting (San Diego)](https://eucrof.eu/24-6-eucrof-jcroa-meeting-san-diego/) - 24/6 EUCROF – JCROA Meeting (San Diego) On the occasion of the DIA Meeting in San Diego, the EUCROF President, Dr Martine Dehlinger-Kremer met the Japanese CRO Association JCROA, chaired by Dr Hisashi Uematsu. Together with Dr Dehlinger-Kremer, EUCROF was represented by Dr Stefano Marini, EUCROF Vice-President (Webex), Mr Yoani Matsakis, EUCROF Treasurer (Webex) and
- [3 - 4/6 - EUCROF General Assembly in Prague](https://eucrof.eu/3-4-6-eucrof-general-assembly-in-prague/) - EUCROF SPRING GENERAL ASSEMBLY – Prague, 3-4 June 2019 The EUCROF Spring General Assembly took place in magical Prague on the 3rd and 4th of June 2019. Attendees had the pleasure of meeting business partners and friends coming from all over Europe and Israel in the astonishing Boccaccio Meeting Room at Grand Hotel Bohemia, the warm welcome
- [16/5 - 2nd Kiev Clinical Research Forum](https://eucrof.eu/16-5-2nd-kiev-clinical-research-forum/) - EUCROF at the 2nd Kiev Clinical Research Forum The 2nd Kiev Clinical Research Forum took place on 16 - 17 May, 2019. The Conference, organized by PHARMASICH (a EUCROF member) with EUCROF’s patronage, was a great success. Over 330 attendees from all over the world, 22 sponsors and booths, speakers from the US, Africa, the
- [27/3 - EUCROF at the EPTRI Meeting](https://eucrof.eu/27-3-eucrof-at-the-eptri-meeting/) - In the framework of the third EPTRI (European Paediatric Translational Research Infrastructure) General Assembly Meeting, held in Madrid on March 27-28th, an Open Day Meeting was organised on March 27th at the Ministry of Health. The meeting has foreseen a dedicated roundtable with the EU Stakeholders held in the afternoon session, involving representatives from Paediatric
- [20/2 - Our last meeting at the EMA in London!](https://eucrof.eu/20-2-our-last-meeting-at-the-ema-in-london/) - Our last meeting at the EMA in London! After many years of visiting London to meet with the EMA, representatives of EUCROF (Dr Martine Dehlinger-Kremer, Dr Dagmar Chase and Simon Lee photographed in the lobby area) attended the very last “EU CT Portal and Union Database” Stakeholder meeting held at the EMA Offices in Canary
- [7/12 - EUCROF Board Elections at their General Assembly (London)](https://eucrof.eu/7-12-eucrof-board-elections-at-their-general-assembly-london/) - Further to the elections at the General Assembly on 7th December 2018 in London, EUCROF is very pleased to announce the Executive Board members for the next mandate (a mandate is over 2 years). Following the progress made in the last 2 years the Board was unanimously re-elected by the Members voting, to serve a
- [24/10 - Stakeholder Meeting at the EMA in London](https://eucrof.eu/24-10-stakeholder-meeting-at-the-ema-in-london/) - The stakeholder Meeting “Shaping regulatory science to 2025” took place at the EMA in London on Wednesday, 24 October 2018. EUCROF attended, represented by Dr Martine Dehlinger-Kremer. The aim of the meeting was to gather insight from stakeholders on the key areas in human medicines to be covered in its ‘Regulatory Science Strategy to 2025’,
- [25-26/10 “Better Medicines for Children”, DIA/EFGCP, Brussels](https://eucrof.eu/25-26-10-better-medicines-for-children-dia-efgcp-brussels/) - On Thursday and Friday next week, the “Better Medicines for Children” Meeting (DIA/EFGCP) will take place in Brussels. EUCROF will be represented by its President, Martine Dehlinger-Kremer, its Vice-President, Dr Stefano Marini, together with Dr Dagmar Chase. Martine Dehlinger-Kremer will be acting as Lead on the Program Committee; she will be providing the Introduction and
- [24/10 - Clinical Trial Facilitation Group (CTFG) at BfArM](https://eucrof.eu/24-10-clinical-trial-facilitation-group-ctfg-at-bfarm/) - The Clinical Trial Facilitation Group (CTFG) Stakeholder Meeting will take place in Bonn on Wednesday, 24 October 2018. The meeting will develop the following topics: EU Clinical Trial Regulation Implementation - Status and Challenges; Innovative (Complex) Trial Design - Follow up; Future Activities and Horizon Scan Clinical Trials – ‘Independent of upcoming CTR’; Burning issues
- [Pharmacovigilance in 2020: Boldly Shaping the Future - Identification of Medicinal Products (IDMP) Implementation.](https://eucrof.eu/pharmacovigilance-in-2020-boldly-shaping-the-future-identification-of-medicinal-products-idmp-implementation/) - 18-08-17-idmp-implementation_eucrof_pv_wgDownload
- [23/1 - One step forward in the recognition of EUCROF’s voice by the scientific community and EU regulators](https://eucrof.eu/23-1-one-step-forward-in-the-recognition-of-eucrofs-voice-by-the-scientific-community-and-eu-regulators/) - On 15 January 2018, EMA and European Network of Centres for Pharmacoepidemiology and Pharmacovigilance, ENCePP*, confirmed the membership of our colleague Dr Xavier Fournie in the ENCePP Working Group 2 “Independence and transparency”. This working group is chaired for ENCePP by Dr Laura Yates (Consultant in Clinical Genetics at the Institute of Genetic Medicine in Newcastle upon
- [24/10 - “The Shifting Perspectives on Pharmacovigilance in Europe”](https://eucrof.eu/24-10-the-shifting-perspectives-on-pharmacovigilance-in-europe/) - Applied Clinical Trials published in its Volume 26, Issue 10, a paper called “The Shifting Perspectives on Pharmacovigilance in Europe” including some highlights and a link to the paper prepared by the EUCROF PharmacoVigilance Working Group on the EUCROF website. http://www.appliedclinicaltrialsonline.com/shifting-perspectives-pharmacovigilance-europe
- [2/10 - New GVP requirement that can have an operational and budget impact to anticipate](https://eucrof.eu/2-10-new-gvp-requirement-that-can-have-an-operational-and-budget-impact-to-anticipate/) - According to recent GVP module VI Revision 2, from 22 NOV 2017 non-serious ADRs from the market in Europe should be submitted to EMA/Eudravigilance within 90 days. This new updated GVP module also applies to non-interventional studies. This may have an impact on on-going studies where non-serious ADRs are collected in CRF but not rapidly
- [1/9 - PV in 2020: boldly shaping the future - part 1](https://eucrof.eu/1-9-pv-in-2020-boldly-shaping-the-future-part-1/) - Future_of_PV_Outsourcing_PART_1_-_1_SEP_2017Download
- [25/4 - Budapest, Dr Dehlinger-Kremer speaking at “Clinical Trials in CEE Forum”](https://eucrof.eu/25-4-budapest-dr-dehlinger-kremer-speaking-at-clinical-trials-in-cee-forum/) - On 25 April 2017, EUCROF, represented by Dr Martine Dehlinger-Kremer, has been invited to speak about the new EU Clinical Trials Regulation at “Clinical Trials in Central &Easter Europe Forum” in Budapest.
- [2/4 - Algier, Dr Marini, attended Round Table “Access to Innovation & Clinical Research”](https://eucrof.eu/2-4-algier-dr-marini-attended-round-table-access-to-innovation-clinical-research/) - On 25 April 2017, EUCROF, represented by Dr Martine Dehlinger-Kremer, has been invited to speak about the new EU Clinical Trials Regulation at “Clinical Trials in Central &Easter Europe Forum” in Budapest.
- [9/5 - Milano, Dr Dehlinger-Kremer speaking at “International Pediatric Clinical Trial Day 2017 - Helping children create lives they deserve”](https://eucrof.eu/9-5-milano-dr-dehlinger-kremer-speaking-at-international-pediatric-clinical-trial-day-2017-helping-children-create-lives-they-deserve/) - EUCROF, represented by Dr Martine Dehlinger-Kremer, will be speaking at the “International Pediatric Clinical Trial Day 2017 - Helping children create lives they deserve” on 09 May 2017 in Milan.
- [12/6 - London, EUCROF attends GCP Inspectors WG meeting (e-source data/ EDC tools) at EMA](https://eucrof.eu/12-6-london-eucrof-attends-gcp-inspectors-wg-meeting-e-source-data-edc-tools-at-ema/) - On 12 June 2017, EUCROF is going to attend as stakeholder the Good Clinical Practice Inspectors Working Group meeting on topics related to e-source data / EDC tools in clinical trials at the EMA in London.
- [9-10/11 - First Kiev Clinical Research Forum – the leading discussing platform for clinical research industry in Eastern Europe](https://eucrof.eu/9-10-11-first-kiev-clinical-research-forum-the-leading-discussing-platform-for-clinical-research-industry-in-eastern-europe/) - The “1st Kiev Clinical Research Forum – the leading discussing platform for clinical research industry in Eastern Europe” will take place on 9 - 10 November 2017. Six speakers from EUCROF invited.
- [Dr. Stefano Marini, invited speaker at CCRA Seminar “UK Clinical Research](https://eucrof.eu/dr-stefano-marini-invited-speaker-at-ccra-seminar-uk-clinical-research/) - Dr. Stefano Marini, EUCROF’s Vice-President, has been invited to present on day two of this seminar being held by our UK members CCRA. The seminar will bring together key stakeholders from Government, Department of Health, regulators, industry experts and the wider community of UK healthcare professionals to deliver unique insights and a roadmap for the
- [The 6th Clinical Research Day organized by AFCROs will take place in the salons of Le Méridien Etoile on 26 January 2017.](https://eucrof.eu/the-6th-clinical-research-day-organized-by-afcros-will-take-place-in-the-salons-of-le-meridien-etoile-on-26-january-2017/) - This event is the meeting place for all stakeholders, professionals and actors in Clinical and Epidemiological Research: institutional, academic, industrial products Health, Cosmetics and Nutrition, CROs, patients and service providers and test support. The day will begin with thematic workshops where the stakeholders of Clinical Research and Monitoring will be invited to exchange, debate and
- [EUCROF has a new Executive Board](https://eucrof.eu/eucrof-has-a-new-executive-board/) - Following elections at last week’s General Assembly in Munich, EUCROF is very pleased to announce the new Executive Board members for the next two years. Dr. Martine Dehlinger-Kremer was elected to the position of President replacing Dr. Stefano Marini, who could not stand again having served the permitted three mandates as President. Dr. Stefano Marini
- [Eucrof contributed in the preparation of the comment document: Consultation on the revision of "Ethical Considerations for Clinical Trials on Medicinal products Conducted with Minors”: a response from Enpr-EMA and partners (30/8).](https://eucrof.eu/eucrof-contributed-in-the-preparation-of-the-comment-document-consultation-on-the-revision-of-ethical-considerations-for-clinical-trials-on-medicinal-products-conducted-with-minors-a-resp/) - Introduction The EU Clinical Trials Regulation 2014 (CTRs) offers a great opportunity to improve research involving children. The supporting document "Ethical Considerations for Clinical Trials on Medicinal products conducted with Minors" is crucial to its implementation and achieving the Regulations’ aims to facilitate research and promote the health of our children and young people (minors).
- [Highlights from the EUCROF General Assembly 1 – 2 December 2015, Athens](https://eucrof.eu/highlights-from-the-eucrof-general-assembly-1-2-december-2015-athens/) - As usual, the representatives of member organizations met at the end of the year. Great thanks to the HACRO colleagues for the organization and support ! Please find hereafter the highlights (PDF) : Athens_GA_articleDownload
- [Press Release - Patient Leaflet 2015](https://eucrof.eu/press-release-patient-leaflet-2015/) - Patient_Leaflet_2015-EN-V6-FINAL-webDownload
- [EUCROF position paper on transparency in early phase clinical research](https://eucrof.eu/eucrof-position-paper-on-transparency-in-early-phase-clinical-research/) - LinkedIn EUCROF released a paper with proposals on the early publication of clinical trial information, balancing the public’s need for transparency and innovators’ intellectual property and confidentiality rights. This paper has been prepared to outline the EUCROF’s position on specific aspects of the implementation of the EU Clinical Trials Regulation for early phase, non-paediatric, non-publicly
- [Summary from the May 2014 Extended Executive Board Teleconference](https://eucrof.eu/summary-from-the-may-2014-extended-executive-board-teleconference/) - 1. Medical Devices Webinars The webinar with the topic of Safety reporting took place on 29.April with a good attendance of 96 people. Certificates of attendance are distributed . Medical Devices regulation webinar will be postponed, will take place in autumn, due to the current status of development of the regulation. 2. The EUCROF Conference Pre-program should be ready in
- [2nd EUCROF Conference - 2/4 February 2015-Paris, France](https://eucrof.eu/2nd-eucrof-conference-2-4-february-2015-paris-france/) - The European Federation of CROs (EUCROF) is pleased to invite you to the forthcoming European Pre-Conference and Conference on Clinical Research that will be held in Paris, France from 2-4 February 2015. Register before 31 October to enjoy EARLY BIRD. www.eucrof-conference.eu Latest News: is there more to clinical procurement than price reduction? For details refer to the conference web site. Les Salons Hoche
- [Press Release - International observational studies](https://eucrof.eu/press-release-international-observational-studies/) - LinkedIn Appplied Clinical Trial Volume 23 Number 23 February March 2014 The Paediatric WG does not only look at the use and timely submission of the Paediatric Investigation Plan in clinical trials in the past years, but also at the main difficulties and constraints of the paediatric research among the European CROs, pharma and ECs.
- [Press Release - How to improve clinical research in children](https://eucrof.eu/press-release-how-to-improve-clinical-research-in-children/) - Appplied Clinical Trial Volume 23 Number 23 February March 2014 The Paediatric WG does not only look at the use and timely submission of the Paediatric Investigation Plan in clinical trials in the past years, but also at the main difficulties and constraints of the paediatric research among the European CROs, pharma and ECs. ACT_Vol23_Number23_FebruaryMarch2014Download
- [EUCROF represented at the EQPA IMP QP Preconference in Vienna](https://eucrof.eu/eucrof-represented-at-the-eqpa-imp-qp-preconference-in-vienna/) - Dagmar Chase has kindly accepted the Invitation as a Guest speaker to EQPA IMP QP Preconference in Vienna 26 Nov 2014. She will speak on behalf of EUCROF about the Clinical Trial Regulation
- [Press Release](https://eucrof.eu/press-release/) - The European CRO Federation (EUCROF), which represents 270 CROs with over 11.000 staff in 12 countries, in close collaboration with the Turkish Association of CROs (SAKDER), which was recently admitted to EUCROF, has organised its first conference/course “CLINICAL TRIALS IN TURKEY - 2012 PERSPECTIVE” Istanbul, February 15th - 16th, 2012. The Turkish government and the

## Pages

- [Homepage](https://eucrof.eu/) - Welcome to EUCROF, the European CROs Federation. We help Contract Research Organizations (CROs) in Europe by improving their knowledge and skills.
- [The EUCROF Federation](https://eucrof.eu/about-the-eucrof-federation/) - The aims and objectives of EUCROF were defined as follows: Promote high quality, Represent the interests of CROs, Close relationship, Training and educational programmes, Distribute information, Exchange of information
- [Working Groups](https://eucrof.eu/working-groups/) - EUCROF encourages the initiatives of its Members to form Working Groups (WGs) which represent a forum for discussion on specific areas of interest for members. Any (Associate) member can contribute to the working groups by nominating a representative.The WGs meet regularly through TCs and/or face to face meetings. In accordance to the focus of each
- [GDPR Code of conduct](https://eucrof.eu/gdpr-code-of-conduct/) - The EUCROF GDPR Code of Conduct for Service Providers in Clinical Research (the Code) is the first transnational code of conduct in the area of health, applicable in all 27 EU Member States.The lead supervisory data protection authority for the Code is the French Data Protection Authority (CNIL).On 29 January 2026 CNIL [here] adopted Resolution
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- [Become a member](https://eucrof.eu/become-a-member/) - Join us!Become a member of EUCROF Federation Become a memberLearn how Become an associate/partnerLearn how New Membership InformationIf you are considering becoming a Member of EUCROF, please read the following:Members of the Federation can exclusively be either legal entities of national Associations of CROs registered in at least one European country, or legal entities of
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- [COVID-19 Pandemic - Further Authorities](https://eucrof.eu/covid-19-pandemic-further-authorities/) - Austria – https://www.basg.gv.at/en/healthcare-professionals/clinical-trials/klinische-studien-und-covid-19/haeufige-fragen Belgium – Coronavirus: Belgische richtsnoer voor het beheer van klinische proeven tijdens de coronaviruspandemie Bulgaria – https://www.bda.bg/en/information-for-companies/1810-recommendations-to-the-sponsors-for-managing-of-clinical-trials-during-the-covid-19-pandemic-and-the-declared-state-of-emergency-in-the-republic-of-bulgaria Croatia – https://zdravlje.gov.hr/ Cyprus – https://www.moh.gov.cy/moh/phs/phs.nsf/dmlindex_en/dmlindex_en?opendocument Czech Republic – http://www.sukl.eu/medicines/opinion-of-sukl-s-department-of-clinical-trials-on-medicinal-1 Denmark – https://laegemiddelstyrelsen.dk/en/news/2020/extraordinary-measures-for-clinical-trials-due-to-covid-19/ Estonia – https://www.ravimiamet.ee/en/guidance-clinical-trial-management-context-covid-19-pandemic Finland – https://www.fimea.fi/web/en/-/clinical-trials-during-the-coronavirus-epidemic-covid-19- France – New guidance for conduct of clinical trials under SARS-CoV-2 / Covid-19 pandemic (2 Nov 2020) France – https://ansm.sante.fr/Activites/Essais-cliniques/Covid-19-Ongoing-clinical-trials Germany (Amendments to COVID-19 Guidelines – 21 May 2020) Germany – https://www.bfarm.de/EN/Drugs/licensing/clinicalTrials/news/CT_COVID19.html Germany (26 March 2020) – dieser
- [COVID-19 Pandemic - FDA](https://eucrof.eu/covid-19-pandemic-fda/) - Conduct of Clinical Trials of Medical Products during the COVID-19 Public Health Emergency (updated Guidance, dated 27 Janury 2021) E-signatures clarified in FDA’s COVID-19 clinical trial guidance “FDA COVID-19 Response” (14 April 2020) “FDA Guidance on Conduct of Clinical Trials of Medical Products during COVID-19 Pandemic”
- [COVID-19 Pandemic - EMA](https://eucrof.eu/covid-19-pandemic-ema/) - On 18 February 2021, the EMA shared its latest publications on COVID-19 vaccines: AstraZeneca European Public Assessment Report (EPAR) EMA receives application for conditional marketing authorisation of COVID-19 Vaccine Janssen EMA starts rolling review of CureVac’s COVID-19 vaccine (CVnCoV) Clarification on Sputnik V vaccine in the EU approval process EMA preparing guidance to tackle COVID-19
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## My Templates

- [Default Kit](https://eucrof.eu/?elementor_library=default-kit)

## Products

- [GCP Inspection](https://eucrof.eu/product/gcp-inspection/)
- [The ICH GCP R3 Roadmap: The Challenge of Vendor Management](https://eucrof.eu/product/the-ich-gcp-r3-roadmap-the-challenge-of-vendor-management/)
- [The ICH GCP R3 Roadmap: Risks management and R3](https://eucrof.eu/product/the-ich-gcp-r3-roadmap-risks-management-and-r3/)
- [MDR, IVDR, and the AI Act: What They Mean for Software as a Medical Device](https://eucrof.eu/product/mdr-ivdr-and-the-ai-act-what-they-mean-for-software-as-a-medical-device/)
- [Insights for Clinical Trial Sponsors: Navigating IVDR 2017/746 and CTR 536/2014](https://eucrof.eu/product/insights-for-clinical-trial-sponsors-navigating-ivdr-2017-746-and-ctr-536-2014/)
- [Unlocking the EU Market: Cost-Effective Strategies for Regulatory & Clinical Success](https://eucrof.eu/product/unlocking-the-eu-market-cost-effective-strategies-for-regulatory-clinical-success/)
- [From Awareness to Enrollment: Can Social Media Close the Gap in Patient Recruitment?](https://eucrof.eu/product/from-awareness-to-enrollment-can-social-media-close-the-gap-in-patient-recruitment/)
- [Electronic Signatures in Clinical Trials - 25 September 2025](https://eucrof.eu/product/electronic-signatures-in-clinical-trials-25-september-2025/)
- [ICH GCP E6(R3): What CRAs Need to Know](https://eucrof.eu/product/ich-gcp-e6r3-what-cras-need-to-know/)
- [Clinical Trials in Armenia, Uzbekistan and Ukraine](https://eucrof.eu/product/clinical-trials-in-armenia-uzbekistan-and-ukraine/)
- [IMPACT – Improving and Acting for a Stronger European Clinical Trials Environment](https://eucrof.eu/product/impact-improving-and-acting-for-a-stronger-european-clinical-trials-environment/)
- [The ICH GCP R3 Roadmap: Changes and Challenges of ICH E6 (R3) – Are you ready?](https://eucrof.eu/product/the-ich-gcp-r3-roadmap-changes-and-challenges-of-ich-e6-r3-are-you-ready/)
- [Navigating the Clinical Hiring Landscape in 2025](https://eucrof.eu/product/navigating-the-clinical-hiring-landscape-in-2025/)
- [20241210 - 10 December 2024 - Clinical Trials in France](https://eucrof.eu/product/10-december-2024-clinical-trials-in-france/)
- [20241029 - 29 October 2024 - Clinical Trial Budget: A Guide to Smart Clinical Expense Planning](https://eucrof.eu/product/29-october-2024-clinical-trial-budget-a-guide-to-smart-clinical-expense-planning/)

## Popups

- [Upcoming webinars](https://eucrof.eu/pixpopup-item/upcoming-webinars/) - Upcoming webinars in 2026 Title Presenter Date Insights for Clinical Trial Sponsors: Navigating IVDR 2017/746 and CTR 536/2014 Amber McNair 21 January 2026 How is the current MDR/IVDR landscape and what opportunities and challenges experience Software as Medical Device apps from the MDR & AI Act MD WG / Dr. Sofoklis Kyriazakos, Innovation
- [Newsletter](https://eucrof.eu/pixpopup-item/newsletter/) - Subscribe to our monthly newsletter EUCROF eNews service facility allows subscribers to stay in touch with all forthcoming events, our numerous achievements and initiatives involving us
- [CRO Details](https://eucrof.eu/pixpopup-item/cro-details/) - Association ID: Country: Address: Website: Affiliation: Core Business: Headcount: Services Provided: Experience In: Therapeutic Areas of Expertise: Areas of Expertise: Geographical Coverage: Other Certifications:
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## Footers

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## Courses

- [GCP Inspection](https://eucrof.eu/elearning/gcp-inspection/) - The presentation will cover trends in site level GCP inspection findings from major health authorities and provide insights on the compliance to ICH GCP E6 R3 guidelines. In addition, I am hoping to deep dive into some proactive initiatives that may help avoid such findings.
- [The ICH GCP R3 Roadmap: The Challenge of Vendor Management](https://eucrof.eu/elearning/the-ich-gcp-r3-roadmap-the-challenge-of-vendor-management/) - ICH E6(R3) introduces a new mindset for oversight of service providers, emphasizing proportionate risk management and systems-based quality rather than procedural compliance. These changes profoundly affect how sponsors – but also CROs – select, qualify, and monitor service providers for clinical trials. This presentation examines how the principles of E6(R3) challenge conventional vendor management by
- [The ICH GCP R3 Roadmap: Risks management and R3](https://eucrof.eu/elearning/the-ich-gcp-r3-roadmap-risks-management-and-r3/) - ICH GCP is changing — and so is the meaning of “risk management.”With ICH GCP R3, regulators are no longer interested in perfect paperwork. They are interested in clear thinking, proportional controls, and real protection of patients and data.This webinar goes beyond theory.What you will really learnThe true risk-management logic of ICH R3 — what
- [MDR, IVDR, and the AI Act: What They Mean for Software as a Medical Device](https://eucrof.eu/elearning/mdr-ivdr-and-the-ai-act-what-they-mean-for-software-as-a-medical-device/) - In this webinar, we will begin with an expert-led overview of the current MDR landscape, presented by the Medical Device Working Group.The regulatory landscape for medical devices (MDs) and in vitro diagnostics (IVDs) devices in Europe has undergone significant changes with the implementation of the Medical Device Regulation (MDR) and the In Vitro Diagnostic Regulation
- [Insights for Clinical Trial Sponsors: Navigating IVDR 2017/746 and CTR 536/2014](https://eucrof.eu/elearning/insights-for-clinical-trial-sponsors-navigating-ivdr-2017746-and-ctr-5362014/) - As the regulatory landscape for clinical trials continues to evolve, sponsors must adapt to the complex requirements introduced by the In Vitro Diagnostic Regulation (IVDR 2017/746) and the Clinical Trials Regulation (CTR 536/2014). This presentation provides a practical overview of the key compliance obligations under both frameworks, with a focus on IVDR compliant clinical trials.
- [Unlocking the EU Market: Cost-Effective Strategies for Regulatory & Clinical Success](https://eucrof.eu/elearning/unlocking-the-eu-market-cost-effective-strategies-for-regulatory-clinical-success/) - An exclusive session on how to design efficient clinical trials through careful budget planning and regulatory guidance for optimal resource allocation, incorporating both strategic designs and tactical monitoring approaches. 🔍 You will learn how to: ✅ Engage with EMA early: Use ITF, Scientific Advice, and ODD for regulatory alignment and optimized trial design ✅ Design efficient trials: Plan recruitment, endpoints,
- [From Awareness to Enrollment: Can Social Media Close the Gap in Patient Recruitment?](https://eucrof.eu/elearning/from-awareness-to-enrollment-can-social-media-close-the-gap-in-patient-recruitment/) - Finding and engaging the right patients for clinical trials remains one of the industry’s greatest challenges—particularly when those patients are underdiagnosed, underrepresented, or unaware that their symptoms may qualify them for participation. In many therapeutic areas, from women’s health to rare diseases, the recruitment journey begins not at the point of consent, but at the
- [Electronic Signatures in Clinical Trials - 25 September 2025](https://eucrof.eu/elearning/electronic-signatures-in-clinical-trials-25-september-2025/) - With the pandemic it became apparent that we use electronic signatures on documents very often. Staff had to stay at home and the home office was even a requirement in some countries. Printing, signing, scanning, mailing the documents for approval and sending the originals with postal mail is tedious. On the other hand the electronic
- [ICH GCP E6(R3): What CRAs Need to Know](https://eucrof.eu/elearning/ich-gcp-e6r3-what-cras-need-to-know/) - The International Council for Harmonisation (ICH) released a revision of its Good Clinical Practice guideline—E6(R3). This update introduces changes with a strong focus on quality by design, critical thinking, and risk-based approaches throughout the clinical trial lifecycle.This webinar is designed specifically for Clinical Research Associates (CRAs) and will explore how the upcoming E6(R3) revision will
- [Clinical Trials in Armenia, Uzbekistan and Ukraine](https://eucrof.eu/elearning/clinical-trials-in-armenia-uzbekistan-and-ukraine/) - The clinical trials landscape is evolving, with a growing shift towards newer, more promising locations. This webinar will explore the recruitment advantages of conducting clinical trials in Armenia, Uzbekistan, and Ukraine. We will discuss the region’s cost-effectiveness, streamlined regulatory processes, and access to diverse patient populations. The session will provide practical insights into recruitment strategies
- [IMPACT – Improving and Acting for a Stronger European Clinical Trials Environment](https://eucrof.eu/elearning/impact-improving-and-acting-for-a-stronger-european-clinical-trials-environment/) - Join us for the launch of IMPACT – a major new initiative from EUCROF designed to reinvigorate the clinical trial landscape in Europe.With Europe experiencing a concerning decline in clinical trials and fewer patients gaining access, EUCROF is stepping up. Launched in December, the IMPACT initiative maps and shares country-level actions aimed at improving trial conditions—and reversing
- [The ICH GCP R3 Roadmap: Changes and Challenges of ICH E6 (R3) – Are you ready?](https://eucrof.eu/elearning/the-ich-gcp-r3-roadmap-changes-and-challenges-of-ich-e6-r3-are-you-ready/) - In the EU, the ICH Guideline E6 (R3) will be effective on 23 July 2025. The guideline underwent a major restructuring and modernisation. The risk-based and risk-proportionate approach has been introduced into every aspect of a clinical trial and modern techniques like the use of computerized systems (e.g., eCRF, eTMF, eConsent), as well as remote
- [Navigating the Clinical Hiring Landscape in 2025](https://eucrof.eu/elearning/navigating-the-clinical-hiring-landscape-in-2025/) - The CRO industry is experiencing a period of volatility, shaped by mergers, acquisitions, and the ongoing push for innovation. While AI-driven platforms and decentralized clinical trials (DCTs) are transforming the landscape, cost-cutting measures among industry giants are adding another layer of complexity.As companies navigate these changes, 2025 is set to be a dynamic and pivotal

## Lessons

- [Replay](https://eucrof.eu/elearning/gcp-inspection/course/replay-13/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate
- [Presentation](https://eucrof.eu/elearning/gcp-inspection/course/presentation-15/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate [pdf-embedder url="https://eucrof.eu/wp-content/uploads/2026/06/0620206EUCROF_GCPInspections.pdf"]Download
- [Survey](https://eucrof.eu/elearning/gcp-inspection/course/survey-4-3-2-2-2/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate
- [Replay](https://eucrof.eu/elearning/the-ich-gcp-r3-roadmap-the-challenge-of-vendor-management/course/replay-12/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate Due to a technical issue, there is no recording available for this webinar.
- [Presentation](https://eucrof.eu/elearning/the-ich-gcp-r3-roadmap-the-challenge-of-vendor-management/course/presentation-14/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate [pdf-embedder url="https://eucrof.eu/wp-content/uploads/2026/04/2026-EUCROF-Ortland-20260415.pdf" title="2026 EUCROF Ortland 20260415"]Download
- [Survey](https://eucrof.eu/elearning/the-ich-gcp-r3-roadmap-the-challenge-of-vendor-management/course/survey-4-3-2-2/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate
- [Replay](https://eucrof.eu/elearning/the-ich-gcp-r3-roadmap-risks-management-and-r3/course/replay-11/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate
- [Presentation](https://eucrof.eu/elearning/the-ich-gcp-r3-roadmap-risks-management-and-r3/course/presentation-13/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate[pdf-embedder url="https://eucrof.eu/wp-content/uploads/2026/03/EUCROF_Risk-and-R3_Lebid.pdf" title="EUCROF_Risk and R3_Lebid"]Download
- [Survey](https://eucrof.eu/elearning/the-ich-gcp-r3-roadmap-risks-management-and-r3/course/survey-4-3-2/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate
- [Presentation](https://eucrof.eu/elearning/mdr-ivdr-and-the-ai-act-what-they-mean-for-software-as-a-medical-device/course/presentation-12/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate[pdf-embedder url="https://eucrof.eu/wp-content/uploads/2026/03/20250226_slides.pdf"]Download
- [Replay](https://eucrof.eu/elearning/mdr-ivdr-and-the-ai-act-what-they-mean-for-software-as-a-medical-device/course/replay-10/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate
- [Survey](https://eucrof.eu/elearning/mdr-ivdr-and-the-ai-act-what-they-mean-for-software-as-a-medical-device/course/survey-4-3/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate
- [Survey](https://eucrof.eu/elearning/insights-for-clinical-trial-sponsors-navigating-ivdr-2017746-and-ctr-5362014-2/course/survey-4-2/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate
- [Presentation](https://eucrof.eu/elearning/insights-for-clinical-trial-sponsors-navigating-ivdr-2017746-and-ctr-5362014-2/course/presentation-11-2/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate[pdf-embedder url="https://eucrof.eu/wp-content/uploads/2026/01/20260121.pdf"]Download
- [Replay](https://eucrof.eu/elearning/insights-for-clinical-trial-sponsors-navigating-ivdr-2017746-and-ctr-5362014-2/course/replay-9-2/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate
- [Survey](https://eucrof.eu/elearning/insights-for-clinical-trial-sponsors-navigating-ivdr-2017746-and-ctr-5362014/course/survey-4/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate
- [Presentation](https://eucrof.eu/elearning/insights-for-clinical-trial-sponsors-navigating-ivdr-2017746-and-ctr-5362014/course/presentation-11/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate[pdf-embedder url="https://eucrof.eu/wp-content/uploads/2026/01/20260121.pdf"]Download
- [Replay](https://eucrof.eu/elearning/insights-for-clinical-trial-sponsors-navigating-ivdr-2017746-and-ctr-5362014/course/replay-9/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate
- [Presentation](https://eucrof.eu/elearning/unlocking-the-eu-market-cost-effective-strategies-for-regulatory-clinical-success/course/presentation-10/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate[pdf-embedder url="https://eucrof.eu/wp-content/uploads/2025/11/slidedeck20251126.pdf"]Download
- [Replay](https://eucrof.eu/elearning/unlocking-the-eu-market-cost-effective-strategies-for-regulatory-clinical-success/course/replay-8/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate
- [Survey](https://eucrof.eu/elearning/unlocking-the-eu-market-cost-effective-strategies-for-regulatory-clinical-success/course/survey-2-3-2-2/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate
- [Replay](https://eucrof.eu/elearning/from-awareness-to-enrollment-can-social-media-close-the-gap-in-patient-recruitment/course/replay-7/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate
- [Presentation](https://eucrof.eu/elearning/from-awareness-to-enrollment-can-social-media-close-the-gap-in-patient-recruitment/course/presentation-9/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate[pdf-embedder url="https://eucrof.eu/wp-content/uploads/2025/11/20251112_Webinar_EUCROFSubjectWell_v07.pdf"] Download
- [Survey](https://eucrof.eu/elearning/from-awareness-to-enrollment-can-social-media-close-the-gap-in-patient-recruitment/course/survey-2-3-2/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate
- [Replay](https://eucrof.eu/elearning/electronic-signatures-in-clinical-trials-25-september-2025/course/replay-6/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate
- [Presentation](https://eucrof.eu/elearning/electronic-signatures-in-clinical-trials-25-september-2025/course/presentation-8/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate[pdf-embedder url="https://eucrof.eu/wp-content/uploads/2025/09/EUCROF-Training-Electronic-Signatures-V1.0.pdf" title="EUCROF Training Electronic Signatures V1.0"] Download
- [Survey](https://eucrof.eu/elearning/electronic-signatures-in-clinical-trials-25-september-2025/course/survey-2-3/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate
- [Replay](https://eucrof.eu/elearning/ich-gcp-e6r3-what-cras-need-to-know/course/replay-5/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate
- [Survey](https://eucrof.eu/elearning/ich-gcp-e6r3-what-cras-need-to-know/course/survey-2/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate
- [Presentation](https://eucrof.eu/elearning/ich-gcp-e6r3-what-cras-need-to-know/course/presentation-7/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate[pdf-embedder url="https://eucrof.eu/wp-content/uploads/2025/09/ICH_GCP_R3_What_CRAs_Need_2_Know_10Sep2025.pdf"] Download
- [Replay](https://eucrof.eu/elearning/clinical-trials-in-armenia-uzbekistan-and-ukraine/course/replay-4/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate
- [Presentation](https://eucrof.eu/elearning/clinical-trials-in-armenia-uzbekistan-and-ukraine/course/presentation-6/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate[pdf-embedder url="https://eucrof.eu/wp-content/uploads/2025/07/Clinical-trials-in-Armenia-Uzbekistan-and-Ukraine_EUCROF_15July2025_final.pdf" title="Clinical trials in Armenia, Uzbekistan, and Ukraine_EUCROF_15July2025_final"] Download
- [Survey](https://eucrof.eu/elearning/clinical-trials-in-armenia-uzbekistan-and-ukraine/course/survey-3-2-2/)
- [Replay](https://eucrof.eu/elearning/impact-improving-and-acting-for-a-stronger-european-clinical-trials-environment/course/replay-3/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate
- [Presentation](https://eucrof.eu/elearning/impact-improving-and-acting-for-a-stronger-european-clinical-trials-environment/course/presentation-5/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate [pdf-embedder url="https://eucrof.eu/wp-content/uploads/2025/07/IMPACT-Mapping-National-Initiatives-to-Enhance-the-Clinical-Trials-Environment-in-Europe.pdf" title="IMPACT-Mapping National Initiatives to Enhance the Clinical Trials Environment in Europe"] Download
- [Survey](https://eucrof.eu/elearning/impact-improving-and-acting-for-a-stronger-european-clinical-trials-environment/course/survey-3-2/)
- [Replay](https://eucrof.eu/elearning/the-ich-gcp-r3-roadmap-changes-and-challenges-of-ich-e6-r3-are-you-ready/course/replay-2/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate
- [Presentation](https://eucrof.eu/elearning/the-ich-gcp-r3-roadmap-changes-and-challenges-of-ich-e6-r3-are-you-ready/course/presentation-4/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate [pdf-embedder url="https://eucrof.eu/wp-content/uploads/2025/06/EUCROF-Webinar_ICH-E6_R3_20250617_final_V2.pdf"] Download
- [Survey](https://eucrof.eu/elearning/the-ich-gcp-r3-roadmap-changes-and-challenges-of-ich-e6-r3-are-you-ready/course/survey-3/)
- [Replay](https://eucrof.eu/elearning/navigating-the-clinical-hiring-landscape-in-2025/course/replay/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate
- [Presentation](https://eucrof.eu/elearning/navigating-the-clinical-hiring-landscape-in-2025/course/presentation-3/) - By completing all sections of the webinar (top right 'Mark as Completed') you will be able to download the certificate [pdf-embedder url="https://eucrof.eu/wp-content/uploads/2025/05/20250514_presentation.pdf"] Download
- [Survey](https://eucrof.eu/elearning/navigating-the-clinical-hiring-landscape-in-2025/course/survey/)
- [Presentation](https://eucrof.eu/elearning/29-october-2024-clinical-trial-budget-a-guide-to-smart-clinical-expense-planning/course/presentation-2/) - Palleos-Budget-Webinar-EUCROF-final
- [Presentation](https://eucrof.eu/elearning/10-december-2024-clinical-trials-in-france/course/presentation/) - EUCROFWebinar_Clinical Trials in France by AFCROs_v1.0

## Portfolio

- [PAREXEL](https://eucrof.eu/partner/parexel/) - EUCROF Member since: 2026PAREXEL Kristine Langelund Country Head – Nordics Kristine.langelund@parexel.com Phone: +4530608334 Parexel Denmark A/S, C/O TMF Denmark A/s H.C Andersens Boulevard 38, 3 th., 1553 København V Denmark
- [DrugCard](https://eucrof.eu/partner/drugcard/) - EUCROF Member since: 2026DrugCard Year of Foundation: 2021 Harju Maakond, Lasnamäe Linnaosa, Ruunaoja tn 3, 11415 – Tallin, Estonia https://www.drug-card.io EUCROF Representative: Dmytro Horilyk dmhorilyk@drug-card.io
- [ACROA - ALBANIAN CRO ASSOCIATION](https://eucrof.eu/partner/acroa-albanian-cro-association/) - EUCROF Member since : 2026ACROA - ALBANIAN CRO ASSOCIATIONYear of foundation: 2026 Rr. e Kavajes, Garden Building, Ap 1A/8/2 1023 – Tirana, Albania https://www.acroa.net EUCROF Representative: Manika Kreka mkreka@acroa.net
- [ATAVES CRO](https://eucrof.eu/partner/ataves-cro/) - EUCROF Member since: 2026ATAVES CRO Esatpaşa Neighborhood, Ziyapaşa Street No:6/1 34704 Ataşehir Istambul Türkiye https://piercro.com/ EUCROF Contact: Zeynep Gultekin Director of Health Services zeynep.gultekin@piercro.com EUCROF Representative: Ridvan Gultekin General Manager ridvan.gultekin@piercro.com
- [Tune Insight](https://eucrof.eu/partner/tune-insight/) - EUCROF Member since: 2026Tune Insight EPFL Innovation Park Building C 1015 Lausanne https://tuneinsight.com/ EUCROF Contact: Juan-Ramón Troncoso-Pastoriza CEO juan@tuneinsight.com EUCROF Representative: Susan Wacklin Head of Growth susan@tuneinsight.com
- [ACRON - Association of Clinical Research Organisations in The Nederlands](https://eucrof.eu/partner/acron-association-of-clinical-research-organisations-in-the-nederlands/) - EUCROF Member since : 2007ACRON - Association of Clinical Research Organisations in The NederlandsYear of foundation: 1995 ACRON secretariat – PriOffice – Kwikstaartlaan 42 – Unit A3943 – 3704 GS ZEIST Phone: +31 (0) 85 029 01 92 E-mail: info@acron.nl https://www.acron.nl President Walter de Kok E-mail: Walter.deKok@iqvia.com Representative for EUCROF Mirjam Huigen
- [The DPO Centre](https://eucrof.eu/partner/the-dpo-centre/) - EUCROF Member since: 2025The DPO Centre 161 Bay Street, Suite 2700, Toronto, Ontario M5J 2S1 Canada Vijzelstraat 68-78 Amsterdam 1017 HL The Netherlands The DPO Centre EUCROF Contact: Tom Cooreman Head of Global Strategic Partnerships Phone: +31 20 209 1510 t.cooreman@dpocentre.com
- [Elderbrook Consulting GmbH](https://eucrof.eu/partner/elderbrook-consulting-gmbh/) - EUCROF Member since: 2025Elderbrook Consulting GmbH Rheinsichtweg 8 8274 Tägerwilen Switzerland https://elderbrook.ch/ EUCROF Contact: Dr Marc Brooks General Manager Phone: +4917682139184
- [CTMS - MKVT (Clinical Trial Management Society Hungary -   Magyarországi Klinikai Vizsgálatszervezők Társasága)](https://eucrof.eu/partner/ctms-mkvt-clinical-trial-management-society-hungary-magyarorszagi-klinikai-vizsgalatszervezok-tarsasaga/) - EUCROF Member since: 2025CTMS - MKVT (Clinical Trial Management Society Hungary - Magyarországi Klinikai Vizsgálatszervezők Társasága) Kaszásdűlő utca 5 fszt. 1033 Budapest Hungary https://mkvt.hu/ EUCROF Contact: Kálmán Töröcsik President kalman.torocsik@mkvt.hu Rokus Kriszt Rokus.Kriszt@sanofi.com
- [CW-Research Management](https://eucrof.eu/partner/cw-research-management/) - EUCROF Member since: 2025CW-Research Management Heilingenstädter Lände 29/2.OG 1190 Vienna Austria https://cw-rm.com/ EUCROF Contact: Christian Wolflehner CEO and owner wolflehner@cw-rm.com Dr Wolfram Adlassnig adlassnig@cw-rm.com
- [Rosenbaum Consulting Ltd](https://eucrof.eu/partner/rosenbaum-consulting-ltd/) - EUCROF Member since: 2025Rosenbaum Consulting Ltd 6-ti Septemvri, 13 ent. B, fl.4, ap. 40 1000 Sofia Bulgaria https://rosenbaum-group.com/ EUCROF Contact: David Rosenbaum Managing Director contact@rosenbaum-group.com
- [Elevate CRO](https://eucrof.eu/partner/elevate-cro/) - EUCROF Member since: 2025Elevate CRO Elevate Klinik Arastirma Danişmanlik Egitim Ve Organizasyon Anonim Sirketi (Turkey) Konutkent Mh. Dumlupınar Blv. Sisa Kule Plaza No:381/84 Çankaya Türkiye https://elevateclinicalresearch.com/ EUCROF Contact: Filiz Hyden Deputy General Manager filiz.hyden@elevate.com.tr
- [Perfection-CRO](https://eucrof.eu/partner/perfection-cro/) - EUCROF Partner since: 2016Perfection-CRO 10 Plaut St. Rehovot Science Park 7670609 Rehovot Israel https://www.perfection-cro.com/ EUCROF Contact Nira Garty Tel: +972 89 316330 Mobile: +972 523 406902 E-mail: nira.garty@perfection-cro.com
- [Phoenix Clinical Research](https://eucrof.eu/partner/phoenix-clinical-research/) - EUCROF Partner since: 2021Phoenix Clinical Research C13 KAPITALIZE Offices, 3rd Floor, Tower 12, Bavaria Town, Ring Road Cairo Egypt https://phoenix-cr.com/ EUCROF Contact Georges Labaki CEO, Phoenix CR Office Phone: + 961 1 429 566 Mobile Phone: + 961 3 672 310 Email: glabaki@phoenix-cr.com
- [Datapharm Australia Pty Ltd](https://eucrof.eu/partner/datapharm-australia-pty-ltd/) - EUCROF Partner since: 2023Datapharm Australia Pty Ltd 56-56A Thompson Street – Drummoyne 2047 NSW Sydney Australia https://datapharmaustralia.com/ EUCROF Contact Luke Edington Clinical Projects Manager Office phone: +61(0)408 206011 Office fax: +61 (0)297192811 E-mail: Luke.Edington@DatapharmAustralia.com
- [Clinica Group](https://eucrof.eu/partner/clinica-group/) - EUCROF Partner since: 2017Clinica Group Cité les Dunes, Domaine propriétaire n°389 / Lotissement n°4 16002 Chéraga, Algiers Algeria https://www.clinicagroup.com/ Representative for EUCROF Mr Salah Eddine Sahraoui E-mail: salah.sahraoui@clinicagroup.com Mrs Christelle Mekaoui Office +213 23 226 607/ +213 982 401 130 Fax: +213 23 226 248 E-mail: christelle.mekaoui@clinicagroup.com
- [Accuracy Research - Health Consulting & Contract Research Organization. Investigación en Salud. Cía. Ltda.](https://eucrof.eu/partner/accurancy-research-health-consulting-contract-research-organization-investigacion-en-salud-cia-ltda/) - EUCROF Partner since: 2025Accuracy Research - Health Consulting & Contract Research Organization. Investigación en Salud. Cía. Ltda. Italia N32-229 and Alemania St., 170519 Quito, ECUADOR https://www.accuracyresearch.com EUCROF Contact Erick Carvajal, Head of Quality Assurance & Clinical Research E-mail: analista.calidad@accuracyresearch.com Dr Adrián Cascante, General Manager Phone: +593 963168476 E-mail: adrian.cascante@accuracyresearch.com
- [NeSPaT](https://eucrof.eu/partner/nespat/) - EUCROF Member since: 2025NeSPaT Ludwika Kondratowicha st. 37a, 03-285 Warsaw, Poland https://nespat.net/ EUCROF Contact: Oleksandr Yefimenkov, Managing Partner Phone: +48884007532 E-mail: o.yefimenkov@nespat.net
- [Wemedoo AG](https://eucrof.eu/partner/wemedoo-ag/) - EUCROF Member since: 2025Wemedoo AG Sumpfstrasse 24, 6312 Stainhausen, Switzerland https://wemedoo.com/ EUCROF Contact: Urosh Vilimanovich, Chief Business and Delivery Officer at Wemedoo. Phone: +381 60 500 5516 Email: urosh.vilimanovich@wemedoo.com
- [SVAROG RESEARCH](https://eucrof.eu/partner/svarog-research/) - EUCROF Member since: 2025SVAROG RESEARCH SVAROG RESEARCH Gunduliceva 22a, 10000 Zagreb, Croatia https://svarogresearch.com/ EUCROF Contact: Ana Stojković, Managing Director Phone: +385 91 460 3602 E-mail: ana.stojkovic@svarogresearch.com
- [PSI CRO](https://eucrof.eu/partner/psi-cro/) - EUCROF Member since: 2025PSI CRO (Austria) Rainergasse 1/5/10, 1040 Vienna, Austria https://psi-cro.com/ EUCROF Contact: Doris Neuhauser, Country Manager AustriaPhone: +43 664 9638963 E-mail: Doris.Neuhauser@psi-cro.com
- [ASCRO - Association of CROs active in Sweden](https://eucrof.eu/partner/ascro-association-of-cros-active-in-sweden/) - EUCROF Member since : 2022ASCRO - Association of CROs active in SwedenYear of foundation: 2022 Sveavägen 63 113 59 Stockholm Sweden https://ascro.se Representatives for EUCROF Helena Lüning Chairman of ASCRO Board ICON Clinical Research Phone: +46 704849555 Email: Helena.Luning@iconplc.com Hedda Magnusson ASCRO Board Member and Treasurer LINK Medical Research Phone: +46 733
- [BeCRO - Belgian Association of CROs](https://eucrof.eu/partner/belgian-association-of-cros-becro/) - EUCROF Member since : 2010BeCRO - Belgian Association of CROsYear of foundation: 2010 Place Marcel Broodthaers plein box 5 1060 Brussels Belgium Phone: Tel: +32 2 892 4000 E-mail: info@becro.be https://www.becro.be President Stéphane Petit Phone: +32 498 91 21 91 E-mail: stephane@becro.be Representative for EUCROF Christophe Golenvaux Phone: +32 477 40 35 14
- [AICRO - Italian Association of CROs](https://eucrof.eu/partner/aicro-italian-association-of-cros/) - EUCROF Member since : 2005AICRO - Italian Association of CROsYear of foundation: 2004 Piazza Meda, 3 20121 Milano Italy https://www.aicro.it President Fabrizio Forini E-mail: presidente@aicro.it Representative for EUCROF Donato Bonifazi Phone: +39 328 7919866 E-mail: ceo@cvbf.net
- [ACRO-Cz - Association of CROs Czech Republic](https://eucrof.eu/partner/acro-cz-association-of-cros-czech-republic/) - EUCROF Member since: 2005ACRO-Cz - Association of CROs Czech RepublicYear of foundation: 2004 Antala Staska 2027/79 Prague 4 Czech Republic Phone: +420 602 713 222 www.acro-cz.cz President and Representative for EUCROF Darina Hrdličková, Director, Clinical Management Phone: +420 233 081 000 E-mail: darinah63@outlook.com
- [ACCSCR – The Association of Companies Conducting Clinical Trials in Romania](https://eucrof.eu/partner/accscr/) - EUCROF Member since : 2019ACCSCR – The Association of Companies Conducting Clinical Trials in RomaniaYear of foundation: 2009 Muzeul Zambaccian Str., 28 Sector 1 Bucharest Romania Representative for EUCROF George Tanaseanu E-mail: George.Tanaseanu@psi-cro.com
- [ULC - Ukrainian Logistic Cluster](https://eucrof.eu/partner/ulc-ukrainian-logistic-cluster/) - EUCROF Member since: 2021ULC - Ukrainian Logistic Cluster Velyka Zhytomyrska Str. 33 01601 Kiev Ukraine http://ulc-health.com/en/ Michael Shumilin, Chairman, ULC Phone/Fax: +38 044 593 06 01 Mobile Phone: +38 095 276 03 33 E-mail: michael.shumilin@ulc-health.com
- [Sermes CRO](https://eucrof.eu/partner/sermes-cro/) - EUCROF Member since: 2023Sermes CRO C/Rufino Gonzaléz, 14 Escalera 1ª – 2º Dcha 28037 Madrid Spain https://sermescro.com/
- [Richmond Pharmacology Limited](https://eucrof.eu/partner/richmond-pharmacology-limited/) - EUCROF Member since: 2015Richmond Pharmacology Limited Cranmer Terrace Tooting, London United Kingdom https://www.richmondpharmacology.com/ EUCROF Contact: Keith Berelowitz, Director of Operations Phone: +44(0)20 8664 5200 E-mail: k.berelowitz@richmondpharmacology.com
- [PharmNDev Experts SA](https://eucrof.eu/partner/pharmndev-experts-sa/) - EUCROF Member since: 2022PharmNDev Experts SA Quai du Seujet 28 1201 Geneva / GE SWITZERLAND https://pharmandev.ch EUCROF Contact: Bernard GOUT, CEO E-mail: bgout@pharmndev.ch
- [PHA FARMED D.O.O.](https://eucrof.eu/partner/pha-farmed-d-o-o/) - EUCROF Member since: 2023PHA FARMED D.O.O. CESTA NA BRDO 100 1000 LJUBLJANA SLOVENIA https://phafarmed.com/ EUCROF Contact: Mrs. SLAVICA ČAMER, CEO Phone: +386 40 873319 email: slavica@phafarmed.com
- [Paspigioni](https://eucrof.eu/partner/paspigioni/) - EUCROF Member since: 2024Paspigioni 86 Abashidze Street, apt. 34 0179 Tbilisi Georgia https://www.paspigioni.com/ EUCROF Contact: Diana MATIASHVILI Founder, company administrator Mobile: +44 7427 950 295 email address: Diana.Matiashvili@paspigioni.com [address of Paspigioni in the UK: 56 Farm Road, N21 3JA London] Nina BIBLAIA Head of Marketing Mobile: +31 6 16209117 email address: Nina.Biblaia@paspigioni.com Paspigioni is conducting clinical trials across phases I –
- [OPTIMAPHARM Croatia](https://eucrof.eu/partner/optimapharm-croatia/) - EUCROF Member since: 2017OPTIMAPHARM Croatia Almeria Business Tower – Ulica grada Vukovara 284 10000 Zagreb Croatia https://optimapharm.eu EUCROF Contact: Miguel Salcedo, PharmD, MBA, PMP Chief Operating Officer Mobile:+34 670 83 63 53 E-mail: miguel.salcedo@optimapharm.eu
- [EVIDENZE Portugal](https://eucrof.eu/partner/evidenze-portugal/) - EUCROF Member since: 2023EVIDENZE Portugal Alameda Fernão Lopes nº16, 7º andar, escritori 1, Miraflores 1495-190 Algés Portugal https://evidenze.com/ EUCROF Contact: Pedro Calheiros Andrade, Country Business Manager Phone: +351912831288 E-mail: p.andrade@evidenze.com
- [D.O. Research Sagl](https://eucrof.eu/partner/d-o-research-sagl/) - EUCROF Member since: 2020D.O. Research Sagl Via G.B. Pioda 9 CH 6901 Lugano Switzerland https://www.doresearch.ch/ EUCROF Contact: Antoinette van Dijk, Managing Director Phone: +41 79 51 17 359 Mobile: +39 335 56083680 E-mail: antoinette.vandijk@doresearch.ch
- [FDA - Food and Drug Administration](https://eucrof.eu/partner/fda-food-and-drug-administration/) - FDA - Food and Drug Administration https://www.fda.gov/ 10903 New Hampshire Avenue MD 20993 Silver Spring US
- [EU Commission](https://eucrof.eu/partner/eu-commission/) - EU Commission https://ec.europa.eu/ Rue de la Loi, 170 1040 Brussels Belgium
- [EFPIA - European Federation of Pharmaceutical Industries Associations](https://eucrof.eu/partner/efpia-european-federation-of-pharmaceutical-industries-associations/) - EFPIA - European Federation of Pharmaceutical Industries Associations https://www.efpia.eu/ Neo Building, Rue Montoyer 51, box 3 1000 Bruxelles TEL: +32 (0)2 626 25 55 Email: reception@efpia.eu
- [EFGCP - European Forum for Good Clinical Practice](https://eucrof.eu/partner/efgcp-european-forum-for-good-clinical-practice/) - EFGCP - European Forum for Good Clinical Practice https://efgcp.eu/ Rue de l’Industrie 4 (Square de Meeûs) B-1000 Brussels Belgium
- [SACROP - Slovak Association of Clinical Research Organizations and Professionals](https://eucrof.eu/partner/sacrop-slovak-association-of-clinical-research-organizations-and-professionals/) - EUCROF Member since : 2015SACROP - Slovak Association of Clinical Research Organizations and ProfessionalsYear of foundation: 2015 V Parku 2343/24 148 00 Bratislava Slovakia https://sacrop.sk Chairman Juraj Gaplovsky MSc. Phone: +420 277 004 800 ext. 6236 Mobile: +420 602 603 413 E-mail: juraj.gaplovsky@psi-cro.com Board Member/Representative Miroslava Šipošová, PharmDr. Bratislavská cesta 100/D, 931 01
- [EMA - European Medicines Agency](https://eucrof.eu/partner/ema-european-medicines-agency/) - EMA - European Medicines Agency www.ema.europa.eu 30 Churchill Place Canary Wharf E14 5EU London United Kingdom
- [ACRO - Association of Clinical Research Organizations](https://eucrof.eu/partner/acro-association-of-clinical-research-organizations/) - ACRO - Association of Clinical Research Organizations www.acrohealth.org 1990 K St., NW Suite 401 20006 Washington, DC US
- [AECIC - Spanish Association of Contract Research Organisations](https://eucrof.eu/partner/aecic-spanish-association-of-contract-research-organisations/) - EUCROF Member since : 2005AECIC - Spanish Association of Contract Research OrganisationsYear of foundation: 2003 C/ Capitan Haya, 1 28020 MADRID Spain https://www.aecic.org President & Representative for EUCROF Óscar Salamanca Gutierrez E-mail: oscar.salamanca@apices.es / presidente@aecic.org
- [AFCROs - Association Française des CROs](https://eucrof.eu/partner/afcros-association-francaise-des-cros/) - EUCROF Member since : 2005AFCROs - Association Française des CROsYear of foundation: 2002 1 Place Paul Verlaine 92100 Boulogne-Billancourt France https://www.afcros.com/ Phone: +33 616 633685 E-mail: contact@afcros.com President Denis COMET mail: dcomet@axonal.com Representative for EUCROF Yoani MATSAKIS mail: yoani.matsakis@tentelemed.com
- [BVMA - Federal Association of Contract Research Organisations](https://eucrof.eu/partner/bvma-federal-association-of-contract-research-organisations/) - EUCROF Member since : 2005BVMA - Federal Association of Contract Research OrganisationsYear of foundation: 1991 Heimeranstr. 35 80339 Munich Germany https://www.bvma.de Phone: +49 89 859 5096 Fax: +49 89 859 5097 E-mail: bvma@bvma.de President & Representative for EUCROF Martin Krauss Phone: +49-89-893 119-25 Fax: +49-89-893 119-20 E-mail: martin.krauss@fgk-cro.de
- [CCRA - Clinical & Contract Research Association](https://eucrof.eu/partner/ccra-clinical-contract-research-association/) - EUCROF Member since : 2005CCRA - Clinical & Contract Research AssociationYear of foundation: 2004 Oadby (P.O. Box 1055) LE2 4XZ Leicester United Kingdom https://www.ccra.org.uk Contact Person Sue Dilks, Director of Operations Phone: +44 116 271 9727 Fax: +44 116 271 3155 E-mail: mail@ccra.org.uk President Atholl Johnston Phone: +44 020 8725 2845 E-mail:
- [HACRO - Hellenic Association of CROs](https://eucrof.eu/partner/hacro-hellenic-association-of-cros/) - EUCROF Member since : 2013HACRO - Hellenic Association of CROsYear of foundation: 2012 4-6, Dimokratias Avenue 154 51 Athens Greece https://www.hacro.gr/ Phone: +30 210 6747361 or +30 210 6747347 President & Representative for EUCROF Evangelia Koraki Phone: + 30 210 8778000 Mobile: +30 6978 182548 E-mail: ekoraki@coronis.gr
- [Lithuanian GCP&RA Association - Lithuanian Good Clinical Practice (GCP) and Regulatory Affairs (RA) Association](https://eucrof.eu/partner/lithuanian-gcpra-association-lithuanian-good-clinical-practice-gcp-and-regulatory-affairs-ra-association/) - EUCROF Member since : 2022Lithuanian GCP&RA Association - Lithuanian Good Clinical Practice (GCP) and Regulatory Affairs (RA) AssociationYear of foundation: 2013 Savanoriu pr. 349 LT-51480 Kaunas Lithuania https://gkrp.lt Representative for EUCROF Egle Kamantauskaite Head of the Association Mobile: +370 687 72852 E-mail: Egle.Kamantauskaite@iconplc.com Migle Geicen Secretary of the Association Tel + 370 6

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