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

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

Supplement zu einer Leitlinie

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.