European Commission Explains Impact Of Brexit On Clinical Trials
The European Commission has outlined various aspects of the clinical trial process that may be affected after the UK withdraws from the EU, and explains how sponsors should prepare.
You may also be interested in...
A draft EU guideline explains how disease registries can be used to supplement evidence in the pre-authorization phase and provide infrastructure for post-authorization evidence generation.
Companies are being encouraged to become “early adopters” of the EU Clinical Trials Information System when it goes live in December 2021.
Drug companies will be able to “play around” with the new EU Clinical Trials Information System in a secure testing environment before it goes live in approximately 15 months.