Conference Details

Medical Device Single Audit Program Preparation

Date :

Place : United States, Fremont

Website :

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!

Medical Device Single Audit Program Preparation will be held in Fremont,United States on date 2018-04-06

Deadline for abstracts/proposals : 5th April 2018

Organized By :161 Mission Falls Lane, Suite 216,

Keynote Speakers :

Venue :Fremont, CA, USA

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Medical Device Single Audit Program Preparation

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