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How To Use The EU’s New Clinical Trial Submission System

Training Offered To Sponsors And National Authorities

 
• By Ian Schofield

From the end of this year, clinical trial sponsors of all shapes and sizes will be able to use the EU’s new centralized trial submissions portal and database. In view of the complexity of the system, practical training sessions as well as online informational materials will be on offer.

Training Courses on Landing Page of Mobile Computer Display
Users will need "skills, capabilities and knowledge" for new clinical trial information system to work well • Source: Shutterstock

The European Medicines Agency is inviting clinical trial sponsors to take part in training programs on how to use the EU’s new centralized clinical trial submission and approval system, which is scheduled to go live at the end of this year.

The clinical trials information system (CTIS) will be a single EU entry point for submitting, assessing, authorizing, supervising and reporting clinical trials. It will include a centralized submission portal and...

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