Author: admin

LinkedIn EUCROF released a paper with proposals on the early publication of clinical trial information, balancing the public’s need for transparency and innovators’ intellectual property and confidentiality rights. This paper has been prepared to outline the EUCROF’s position on specific...

1. Medical Devices Webinars The webinar with the topic of Safety reporting took place on  29.April with a good attendance of  96 people. Certificates  of attendance are distributed . Medical Devices regulation webinar will be postponed, will take place in autumn, due to the...

The European Federation of CROs (EUCROF) is pleased to invite you to the forthcoming European Pre-Conference and Conference on Clinical Research that will be held in Paris, France from 2-4 February 2015. Register before 31 October to enjoy EARLY BIRD. www.eucrof-conference.eu Latest News: is there more to...

LinkedIn Appplied Clinical Trial Volume 23 Number 23 February March 2014 The Paediatric WG does not only look at the use and timely submission of the Paediatric Investigation Plan in clinical trials in the past years, but also at the...

Appplied Clinical Trial Volume 23 Number 23 February March 2014 The Paediatric WG does not only look at the use and timely submission of the Paediatric Investigation Plan in clinical trials in the past years, but also at the main...

Dagmar Chase has kindly accepted the Invitation as a Guest speaker to EQPA IMP QP Preconference in Vienna 26 Nov 2014. She will speak on behalf of EUCROF about the Clinical Trial Regulation

The European CRO Federation (EUCROF), which represents 270 CROs with over 11.000 staff in 12 countries, in close collaboration with the Turkish Association of CROs (SAKDER), which was recently admitted to EUCROF, has organised its first conference/course “CLINICAL TRIALS IN...