Post Market Surveillance for Medical Devices

Date: March 22 2012

Location: Virtual

Website: http://bit.ly/vZbpqr

About This Event

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@globalcompliancepanel.com
http://www.globalcompliancepanel.com

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

Sign Up!

http://bit.ly/vZbpqr

Tags

fsca, fsn, iso 13485, iso 14971, mdd annex x, medical devices, online training, post market surveillance, qsr