2018 Highlights Include:
Your one stop shop for the latest clinical evaluations and investigations updates
- New clinical considerations under the MDR: Competent Authority, Notified Body and industry updates
- Best practice for applying the new MEDDEV 2.7.1 rev 4 guidance
- Are your Post Market Clinical Follow-Up activities up to scratch?
- Explore clinical evidence requirements for class III devices in the MDR
- How do EUDAMED developments impact clinical evaluations and investigations?
Competent Authority and Notified Body perspectives from:
- Health Products Regulatory Authority
- TÜV SÜD Product Service GmbH
- UL International (UK) Ltd.
- TÜV Rheinland LGA Products GmbH
You’ve got questions. We’ve got the answers.
We’ll be hosting interactive panel discussions on:
- Sharing experiences with writing a CER following MEDDEV 2.7.1 rev 4
- Open floor Q&A session – save up your questions from the day to ask our panel
- A chance to catch up with Competent Authority, Notified Body and industry experts