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