Guidelines for Regulatory Auditing of Quality Systems of Medical Device Manufacturers: General Requirements - Supplement No. 4 - Compilation of Audit Documentation (Clause 5.7)

Titel:
Guidelines for Regulatory Auditing of Quality Systems of Medical Device Manufacturers: General Requirements - Supplement No. 4 - Compilation of Audit Documentation (Clause 5.7)
Herkunft/Verlag:

GHTF http://www.ghtf.org/documents/sg4/sg4-n9924r3.pdf

Dokumentenart:
Guidance
Inhalt:
Die Guideline ergänzt das GHTF Dokument Guidelines for Regulatory Auditing of Quality Systems of Medical Device Manufacturers: General requirements

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