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.
Past Events
Medical Device Regulations in Europe 2012 - 25-26 Sep 2012, The Rembrandt Hotel, London, United Kingdom (17450)
Medical Device Regulations in Europe 2026
Important
Please, check "Medical Device Regulations in Europe" official website for possible changes, before making any traveling arrangements
