News Summary

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...

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...

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...

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...

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...

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:  These white papers were written by a joint task...

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...

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...

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...

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...