Category: Articles

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...

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...

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...

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...

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...

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...

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...

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)...

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...

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...