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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,...

The EUCROF Talent Engagement Task Force introduces itself: Let us meet the Task Force and discover what are its activities and goals!

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...

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...

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...

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...

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 &...

Three White Papers released bythe Archiving andthe Decommissioning Team​EUCROF & the eClinical Forum Archiving and Decommission Team are pleased to announce the public release of three white papers: These white papers were written by a joint task force from EUCROF and the...

Propositions onRemote Source Data Verification andRemote Source Data ReviewA 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...

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...