Geneva, Switzerland, September 07, 2012 --(PR.com
)-- The objective of this 45-minute complimentary webinar is to inform manufacturers of the likely changes they will start to experience in audits and technical documentation reviews from Notified Bodies. These changes are starting to occur now and will continue to be introduced during 2013.
Why is Change Needed?
Where and How are these Changes being Agreed?
Changes to Audits and Actions for Manufacturers
Changes to Technical File Reviews and Actions for Manufacturers
Opportunity for Question and Answers
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 Active Implantable Medical Devices, 93/42/EEC Medical devices and 98/79/EC In Vitro Diagnostic 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. Chris Jepson BSc., FCQI, MIMMM, C Eng SGS Global Manager- Medical Devices
Register for session 1 here (https://sgseventcenter.webex.com/sgseventcenter/onstage/g.php?t=a&d=703825144)
09:00 a.m. London
10:00 a.m. Paris, Berlin, Madrid, Amsterdam
04:00 a.m. New York
04:00 p.m. Singapore, Kuala Lumpur
Register for session 2 here (https://sgseventcenter.webex.com/sgseventcenter/onstage/g.php?t=a&d=702279169)
02:00 p.m. London
03:00 p.m. Paris, Berlin, Madrid, Amsterdam
09:00 a.m. New York
09:00 p.m. Singapore, Kuala Lumpur
Cost: No Charge
For more information, please contact:
SGS Global Manager- Medical Devices
202B Worle Parkway, Weston-super-Mare, BS22 6WA, UK
Event location: Online