Date :
Place : United States, Fremont
Contact Person:Event Manager
Description:
Overview: The International Medical Device Regulators Forum (IMDRF) recognizes that a global approach to auditing and monitoring the manufacturing of medical devices could improve their safety and oversight on an international scale. Why should you Attend: Today with a single audit, it is possible for a medical device manufacturer to satisfy the quality management system requirements of Australia, Brazil, Canada, Japan and the USA!Deadline for abstracts/proposals : 5th April 2018
Organized By :161 Mission Falls Lane, Suite 216,
Keynote Speakers :
Venue :Fremont, CA, USA
Check the event website for more details.