News Summary

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...

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...

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...

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)...

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...

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,...

“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...

“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...

“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...

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...