How to prepare your submission package
Learn from our experienced clinical development consultants which documents are required, what to consider and how to avoid delays.
In this session, you will an overview on the documents and process required. It is teaser for the upcoming Key2Compliance training/course on Medical Device Clinical Investigations in May.
- Which documents are required
- About the preparations and approval process
- Lessons learned
Who should attend
This session is suitable for all medical device professionals that are planning/would like to learn more about clinical investigations