Transcription of Quality Management systems - Process Validation …
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GHTF/SG3/N99-10:2004 (Edition 2) FINAL DOCUMENT Title: Quality Management systems - Process Validation guidance Authoring Group: SG3 Endorsed by: The Global Harmonization Task Force Date: Edition 2 - January 2004 Taisuke Hojo, GHTF Chair The document herein was produced by the Global Harmonization Task Force, a voluntary group of representatives from medical device regulatory agencies and the regulated industry. The document is intended to provide non-binding guidance to regulatory authorities for use in the regulation of medical devices, and has been subject to consultation throughout its development.
GHTF Study Group 3 - Quality Management Systems Process Validation Guidance – January 2004 Page 2 Process Validation Guidance Contents 0 Introduction
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Process Validation for Medical Devices, Guidance, Process Validation, 23 STERILE MEDICAL DEVICE PACKAGE, 23 STERILE MEDICAL DEVICE PACKAGE DEVELOPMENT, PROCESS, GUIDELINE ON SUBMISSION OF, GUIDELINE ON SUBMISSION OF MANUFACTURING PROCESS VALIDATION, MEDICAL DEVICE REGULATION PRE-MARKET, MEDICAL DEVICE REGULATION PRE-MARKET APPROVAL, Medical Device