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Overview: Year after year, CAPA is the subsystem cited most frequently during FDA inspections. A robust Corrective and Preventive Action (CAPA) program is of the utmost importance to a medical device manufacturer.
Date :
Place : United States, Fremont
Contact Person:Event Manager
Description:
Overview: Year after year, CAPA is the subsystem cited most frequently during FDA inspections. A robust Corrective and Preventive Action (CAPA) program is of the utmost importance to a medical device manufacturer.Overview: Year after year, CAPA is the subsystem cited most frequently during FDA inspections. A robust Corrective and Preventive Action (CAPA) program is of the utmost importance to a medical device manufacturer. will be held in Fremont,United States on date 2017-06-19
Deadline for abstracts/proposals : 18th June 2017
Organized By :Compliance4All
Keynote Speakers :
Venue :Fremont, CA, United States
Check the event website for more details.
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