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CERTIFICATION EXAMINATION IN MULTIPLE SCLEROSIS INFORMATION AND REFERRAL Handbook for Candidates EXAMINATION DATES Spring 2013 Application Deadline February 1, 2013, Testing Window Begins: March 16,
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What is mscir?
MSCIR stands for Medical Device Single Audit Program (MDSAP) Corrective Action Request (CAR) Initiation Report. It is a form used to initiate corrective actions in response to non-conformities identified during an MDSAP audit.
Who is required to file mscir?
Medical device manufacturers participating in the Medical Device Single Audit Program (MDSAP) are required to file an MSCIR if non-conformities are identified during an MDSAP audit.
How to fill out mscir?
The MSCIR form should be completed with all required information regarding the non-conformities identified during the MDSAP audit, including a detailed description of the non-conformity, its root cause, and proposed corrective actions.
What is the purpose of mscir?
The purpose of MSCIR is to formally initiate corrective actions to address non-conformities identified during an MDSAP audit, ensuring compliance with applicable medical device regulations and standards.
What information must be reported on mscir?
The MSCIR form should include information such as the identification of the non-conformities, their classification, a description of the non-conformity, the root cause analysis, and proposed corrective actions.
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