ISO 13485:2016 – Understanding Changes and Requirements
Published on March 1, 2016, ISO 13485:2016 updates the international medical devices quality management systems standard. Join this webinar to learn about the changes and to hear an interpretation of the impact for manufacturers.
August 8, 2016
August 8, 2016
This webinar is part of the SGS service to keep manufacturers up to date with changes in the regulatory framework.
This is specific to the new revision of ISO 13485:2016 which was published on March 1, 2016.
It will cover the changes and new themes in this update to ISO 13485. The agenda of this presentation will consist of the following:
- Structure & terminology
- Key changes to ISO 13485
- Future development
Dr. Andrew Norrish, Technical Manager, Global Medical Devices
Andrew Norrish has responsibility for providing technical support to enhance the service capability of the SGS Global Medical Device activities. Andrew has more than 12 years experience in the medical device industry and previously held Quality & Regulatory roles in medical device and IVD manufacturing. Prior to medical devices, Andrew worked in pharma operations within A.P.I. manufacturing.
The webinar presentation will also be supported by: Mr. Kevin Butcher, Operations Manager, Global Medical Devices
This free webinar will be conducted in English.
For further information, please contact:
Joanna Marie Caumeran
SGS Global Marketing Services Coordinator
t: +63 (2) 848 0777