The EU Regulation No 536/2014 on “clinical trials on medicinal products for human use” was issued in April 2014. It regulates the planning, performing and evaluating of clinical trials in the EU, which are fully compliant with good clinical practice. This new regulation implements now a single application and approval process. This Online training will provide the new EU Clinical Trial Regulation requirements. #webinar
Key learnings:
Understand
Prevent Inspection Findings
Changes for Trials in the EU
Delegated acts and other Implementation Documents
Authorisation Process
Create Successful Implementation
Share This Event