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Guidelines for Regulatory Auditing of Quality Systems of Medical Device Manufacturers Supplement No. 3: Training Requirements for Auditors:2000

Origin/Publisher:

GHTF

Document Type:
Supplement to a guideline
Content:
The document describes in more detail training elements required to:i prepare an individual to be an auditor; ii qualify auditors to conduct regulatory audits of medical device manufacturers’ quality systems; and iii maintain their qualifications.

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