2012 - Post Market Surveillance for Medical Devices - Webinar By GlobalCompliancePanel

Overview: 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.

Why you should attend: Post market surveillance can be complicated, but by breaking it down into its parts, it can be accessible. With the understanding of the parts, you can develop and implement a comprehensive system that will help you stay in compliance. By attending this webinar, you will find out what you need to do and be well on the way to effective performance.

Areas Covered In the Session:
The Structure of Post Market Surveillance
US System
Complaints (QSR)
Medical Device Reports
Corrections and Removals
International Systems
Complaints (ISO 13485)
EU Vigilance
EU FSCA and FSN
Canada Adverse Event Reporting
Post Production Information Collection
Risk Management (ISO 14971)
Clinical Evaluation (MDD Annex X)
Who will benefit:
Quality Managers
Regulatory Affairs Managers
Risk Managers
Design Control Managers

Price List:
Live : $245.00
Corporate live : $995.00
Recorded : $295.00

webinars-AT-globalcompliancepanel.com
http://www.globalcompliancepanel.com

Phone: 800-447-9407
Fax: 302-288-6884