MEDICAL DEVICES: SAFETY ASSESSMENT AND NEW REGULATION
Date: 08/03/2018 - 08/03/2018
One-day seminar focusing on documenting the safety of medical devices and the importance of the safety assessment in connection with CE marking. We will cover regulatory requirements, problematic substances (CMR substances) and testing, including the challenge of extractables and leachables substances. Speakers from industry and the supply chain will give examples of how to meet product compliance.