Study Group 4: Auditing Guidelines for Regulatory Auditing of Quality Systems of Medical Device Manufacturers Supplement No. 3: Training Requirements for Auditors:2000 FINAL DOCUMENT - International Register of Certificated Auditors - Document - PDFSEARCH.IO

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	Study Group 4: Auditing Guidelines for Regulatory Auditing of Quality Systems of Medical Device Manufacturers Supplement No. 3: Training Requirements for Auditors:2000 FINAL DOCUMENT Add to Reading List Document Date: 2012-11-13 17:53:08 Open Document File Size: 71,50 KB Share Result on Facebook Company Auditors Authoring Group / / IndustryTerm medical device manufacturers / medical device manufacturer / tissue processing / specialised technologies / medical device manufacturing / manufacturing processes / voluntary / regulatory audits / / Organization Global Harmonization Task Force / / Person Beth Pieterson / / Position General / Chair / auditor / experienced auditor coach / experienced auditor / individual auditor / / Technology related technologies / / SocialTag Business Audit Quality audit Evaluation Environmental audits International Register of Certificated Auditors Auditing Risk Global Harmonization Task Force

Study Group 4: Auditing Guidelines for Regulatory Auditing of Quality Systems of Medical Device Manufacturers Supplement No. 3: Training Requirements for Auditors:2000 FINAL DOCUMENTAdd to Reading List