Webinar Update: "Clinical Evaluation: Current Challenges and Best Practice"

Geneva, Switzerland, November 09, 2012 --(PR.com)-- The objective of this 45-minute complimentary webinar is to is to inform manufacturers of current challenges in meeting the needs of Annex X of 93/42/EEC, and utilization of European Commission guidance to address requirements.

Agenda

1. Essential Requirements and Annex X
2. Current issues identified with clinical evaluations
3. Pre-CE marking requirements for clinical evaluation
4. Post market clinical follow-up activities
5. Opportunity for Questions and Answers

Target Audience

This complimentary webinar is aimed at medical device manufacturers and organizations who have certification under one of the European medical device directives or who plan to obtain such certification. The relevant directives are 90/385/EEC Active Implantable Medical Devices and 93/42/EEC Medical Devices. Those people involved with or responsible for quality systems, regulatory affairs, product design, manufacture or clinical activities will find the subject relevant.

Presenter
Mr. Adrian Keene - SGS Clinical Affairs and Regulatory Manager

Register for session 1 here (https://sgseventcenter.webex.com/sgseventcenter/onstage/g.php?d=706950187&t=a)
08:00 a.m. London
09:00 a.m. Paris, Berlin, Madrid, Amsterdam
03:00 a.m. New York
04:00 p.m. Singapore, Kuala Lumpur

Register for session 2 here (https://sgseventcenter.webex.com/sgseventcenter/onstage/g.php?d=702028167&t=a)
01:00 p.m. London
02:00 p.m. Paris, Berlin, Madrid, Amsterdam
08:00 a.m. New York
09:00 p.m. Singapore, Kuala Lumpur

Language: English
Cost: No Charge