Medical Device 2012 - Acceptance Activities in FDA QSR ? Regulations and Warning Letters
Date2012-04-13
Deadline2012-04-13
VenuePalo Alto, USA - United States
KeywordsAcceptance Activities, FDA QSR, Warning Letters, Quality Management System, acceptance criteria, acceptance records, record keeping, medical device manufacturing
Topics/Call fo Papers
This webinar will explain the FDA QSR requirements for acceptance activities related to medical device manufacturing. It clarifies FDA’s intent using the preamble to the regulations.
Why Should You Attend:
Acceptance activities are common in device manufacturing, but seem to cause problems for some manufacturers. These problems range from simple instances of lack of procedures or acceptance criteria to misapplication of statistical methods.
Other CFPs
Last modified: 2012-03-06 17:40:07