Guidelines for Regulatory Auditing of Quality Systems of Medical Device Manufacturers General Requirements Supplement No. 4 Compilation of Audit Documentation (Clause 5.7) SG4 N(99)24R3 Study Group 4 – Final Document G - Single supplement - Document - PDFSEARCH.IO

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	Guidelines for Regulatory Auditing of Quality Systems of Medical Device Manufacturers General Requirements Supplement No. 4 Compilation of Audit Documentation (Clause 5.7) SG4 N(99)24R3 Study Group 4 – Final Document G Add to Reading List Document Date: 2012-11-13 17:53:09 Open Document File Size: 61,50 KB Share Result on Facebook Company Authoring Group / / IndustryTerm voluntary / medical devices / / Organization Global Harmonization Task Force / / Position General / auditor / Chair / / SocialTag Risk Global Harmonization Task Force Medical equipment Audit Business Corporate governance Single Audit Information technology audit process Clinical audit Auditing

Guidelines for Regulatory Auditing of Quality Systems of Medical Device Manufacturers General Requirements Supplement No. 4 Compilation of Audit Documentation (Clause 5.7) SG4 N(99)24R3 Study Group 4 – Final Document GAdd to Reading List