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This webinar will discuss challenges that medical device manufacturers face in meeting the needs of Annex X of 93/42EEC and explain how European Commission guidance can be used to address requirements.


November 28, 2012


November 28, 2012



SGS invites you to attend the  45-minute complimentary webinar "Clinical Evaluation: Current Challenges and Best Practice" on 28 November 2012.
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.


  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.


Mr. Adrian Keene - SGS Clinical Affairs and Regulatory Manager

Register for session 1 here
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 
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

For more information, please contact:

Nelirene Dablio
Global Interactive Marketing Manager
t: +63 2 848 0777 loc. 8772

Language: English
Cost: No Charge