Transcription of ICH HARMONISED TRIPARTITE GUIDELINE
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INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL. REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE. ICH HARMONISED TRIPARTITE GUIDELINE . GOOD manufacturing PRACTICE GUIDE FOR. active PHARMACEUTICAL INGREDIENTS. Q7. Current Step 4 version dated 10 November 2000. This GUIDELINE has been developed by the appropriate ICH Expert Working Group and has been subject to consultation by the regulatory parties, in accordance with the ICH Process. At Step 4 of the Process the final draft is recommended for adoption to the regulatory bodies of the European Union, Japan and USA. Q7.
GOOD MANUFACTURING PRACTICE GUIDE FOR ACTIVE PHARMACEUTICAL INGREDIENTS 1. INTRODUCTION 1.1 Objective This document (Guide) is intended to provide guidance regarding good manufacturing
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Good manufacturing practice for active, Good manufacturing practices for biological, Good manufacturing practices for biological products, Guidance, Active, Certified Pharmaceutical Good Manufacturing, ICH Q7, Guidance on the homeopathic medicinal products, The homeopathic medicinal products dossier