If you wish to know more about the next webinars and trainings
14 October 2026 – The EU Biotech Act and FAST-EU: Accelerating Clinical Research in Europe
Webinar Date & Time 14 October 2026 from 11:00 AM to 12:30 PM (CEST) Webinar Overview On 16 December 2025, the European Commission proposed the EU Biotech Act, a package of measures designed to improve public health while strengthening the...
17 September 2026 – How CROs can Select and Scale the Right AI Technologies
Webinar Date & Time 17 September 2026 from 11:00 AM to 12:30 PM (CEST) Webinar Overview Technology decisions are becoming central to how CROs improve delivery, strengthen performance and create greater value for sponsors. Yet not every technology serves the...
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...
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...
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...
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...
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....
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...
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...
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...
