Transcription of GUIDE TO GOOD MANUFACTURING PRACTICE FOR …
{{id}} {{{paragraph}}}
Example: bankruptcy
GUIDE TO GOOD MANUFACTURING PRACTICE FOR …
PHARMACEUTICAL INSPECTION CONVENTION PHARMACEUTICAL INSPECTION CO-OPERATION SCHEME pe 009 -8 ( part I) 15 January 2009 pe 009 -8 ( part I) 15 January 2009 GUIDE TO good MANUFACTURING PRACTICE FOR medicinal PRODUCTS part I PIC/S January 2009 Reproduction prohibited for commercial purposes. Reproduction for internal use is authorised, provided that the source is acknowledged. Editor: PIC/S Secretariat 14 rue du Roveray CH-1207 Geneva e-mail: web site: pe 009 -8 ( part I) - i - 15 January 2009 TABLE OF CONTENT CHAPTER 1 - QUALITY 1 1 Quality 1 good MANUFACTURING PRACTICE for medicinal products (GMP).. 2 Quality 3 Product Quality 4 Quality Risk 5 CHAPTER 2 - 7 7 7 Key Personnel .. 7 Training .. 9 Personal Hygiene .. 9 CHAPTER 3 - PREMISES AND 11 11 11 11 Production 11 Storage 13 Quality Control 13 Ancillary 14 Equipment.
Chapter 1 Quality Management PE 009-8 (Part I) - 1 - 15 January 2009 CHAPTER 1 QUALITY MANAGEMENT PRINCIPLE The holder of a manufacturing authorisation must manufacture medicinal
Loading..
Tags:
Information
Domain:
Source:
Link to this page:
Please notify us if you found a problem with this document: