Post Market Surveillance for Medical Devices - Webinar By ComplianceOnline (Medical Devices)

Venue: Online Event

Location: Palo Alto, California, United States

Event Date/Time: Sep 26, 2012 End Date/Time: Sep 26, 2012
Report as Spam


This 90-minute webinar covers all aspects of post market surveillance (PMS) for medical devices. It will direct you to the specific documents for the detailed information you need for an effective post-market surveillance system.

Why Should You Attend:

Post market surveillance is changing, not only in the US, but also in the EU and Canada. New rules and regulations are emerging in the countries where the devices manufacturers market their products. The sheer volume of rules and regulations can be daunting, but the differences in each geographic market can be scary.

This webinar explains the aspects of post market surveillance that will help you understand and implement them. The webinar explains the use of post-market surveillance in maintaining your risk management file (ISO 14971) and updating your clinical evaluation (MDD Annex X). In addition, the webinar compares and contrast the rules for adverse event reporting in the US, EU, and Canada.


Online Event
2600 E. Bayshore Road
Palo Alto
United States