News Summary

Press Release17 March 2021The European CRO Federation (EUCROF), announces the submission for approval by the Data Protection Authorities of the 27 EU Member States and the European Data Protection Board, of its GDPR Code of Conduct for Service Providers in...

eConsent Implementation GuideThe EUCROF and eClinical Forum Electronic Informed Consent (eConsent) Joint Task Force are pleased to announce the publication of the eConsent Implementation Guide (version 1). The joint task force was formed in 2019 with a view to look...

The archiving of clinical trial records is a required process that is in need of future direction to meet current business models as well as regulatory and legal expectations.  A group of industry experts coalesced under EUCROF and the eClinical...

The Current Status of European Research Related to COVID-19:The EUCROF PerspectiveThe unexpected SARS-CoV-2 impacted on all aspects of ordinary life especially when it comes to research activities.To face COVID-19 pandemic, many hospitals have been forced to drastically change their organisation...

Last week EUCROF held its Fall General Assembly for 2020. Due to the continued travel restrictions associated to the ongoing COVID-19 pandemic, the GA was held remotely on 3rd and 4th December. It was attended by over 40 participants, which...

On 03 December 2020, EUCROF President, Dr Martine Dehlinger-Kremer, is going to attend the Annual Duchenne Patient Academy Conference, taking place from 30 November to 06 December 2020. This year it is a virtual event.39 patient organizations will participate, 52...

Dear EUCROF Affiliates,As you might know, my University (Università del Piemonte Orientale, Novara, Italy), together with the Universitad Miguel Hernandez (Spain), the Université de Namur (Belgium), the Université de Liege (Belgium), and Humboldt Universität (Germany), are running a European Master financed...

This year, the Annual Clinical Trials Symposium “2020: A YEAR OF UNPRECEDENTED CHALLENGES IN CLINICAL RESEARCH”, under the patronage of EUCROF, will take place from Romania as a virtual conference.Dr Martine Dehlinger-Kremer, President of EUCROF, is going to hold the...

The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) issued a dozen documents explaining how medicines licensure will work after the Brexit transition period expires on 1 January 2021.

EUCROF is excited to post the second Podcast on the topic:“Validation of Computerized Systems in GCP Environment​”Hear from two experts Simone Bucerius, member of the EUCROF Events & Training Working Group, and her colleague at FGK Clinical Research GmbH, Guenter...