Topics
- Proposed changes and the implications for industry
- The latest on the European Legislation
- Clinical assessment requirements
- Notified Bodies expectations
- The closing gap on Human Tissue Products
- Where to gain scientific advice
- The increased focus on vigilance, PMS and patient safety
Who should Attend
Personnel from the medical device industry involved in Regulatory Affairs, Business Development, Quality Assurance, Registration, Manufacturing, Marketing, Technical Affairs and R&D.
