ISO 14971 Risk Management: Industry Procedures and Best Practices

From the high-level implications in the Medical Device Directives (93/42/EEC and 98/79/EC) to the harmonized requirements of Annexes ZA, ZB and ZC, manufacturers are struggling to implement a compliant system that is also sustainable and practical. This webinar offers a unique opportunity to hear the latest industry thinking on the implementation of ISO 14971. Recorded August 24, 2016