Transcription of EU Guide to Good Manufacturing Practice for …
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EU Guide to Good Manufacturing Practice for …
EU Guide to good Manufacturing Practice for Medicinal Products GE036a gggmmmpppeeeyyyeee 1 EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL SANCO/C8/AM/sl/ares(2010)1064603 EudraLex The Rules Governing Medicinal Products in the European Union Volume 4 good Manufacturing Practice Medicinal Products for Human and Veterinary Use Explanatory Notes on the Preparation of a Site Master File These notes are intended to provide guidance on the recommended content of the Site Master File. A requirement for a Site Master File is referred to in Chapter 4 of the GMP Guide . SMF . SMF GMP 4 . Status of the document: New EU Guide to good Manufacturing Practice for Medicinal Products GE036a gggmmmpppeeeyyyeee 2 1.
EU Guide to Good Manufacturing Practice for Medicinal Products GE036A ggmmmppeeyyyeee www.gmpeye.co.kr 3 becomes effective and the date by which it …
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