GOOD MANUFACTURING PRACTICES FOR …
working document qas/08.256 rev.1 page 2 schedule for the proposed adoption process of document qas/08.256: guideline on good manufacturing practices for pharmaceutical
Download GOOD MANUFACTURING PRACTICES FOR …
Information
Domain:
Source:
Link to this page:
Documents from same domain
INVESTING IN HEALTH FOR ECONOMIC …
www.who.int2 INVESTING IN HEALTH FOR ECONOMIC DEVELOPMENT Report by the Mexican Commission on Macroeconomics and health 3 The …
WHO GOOD PRACTICES FOR PHARMACEUTICAL …
www.who.intworking document qas/09.297/rev.2 page 2 schedule for the proposed adoption process of document qas/09.297/rev.2: who good practices for pharmaceutical microbiology laboratories
NORMES ET STANDARDS EN INFRASTRUCTURES …
www.who.intnormes et standards en infrastructures et equipements du centre de sante et de promotion sociale, du centre medical avec antenne chirurgicale et du …
Heterotrophic Plate Count Measurement in …
www.who.intWorld Health Organization Sustainable Development and Healthy Environments Heterotrophic Plate Count Measurement in Drinking Water Safety Management
Annex 3 WHO good manufacturing practices for ...
www.who.int96 Introduction The fi rst WHO draft text on good manufacturing practices (GMP) was prepared in 1967 by a group of consultants at the request of the Twentieth
Annex 5 WHO good distribution practices for …
www.who.int236 1. Introduction Distribution is an important activity in the integrated supply-chain management of pharmaceutical products. Various people and entities are
Annex 2 WHO good practices for pharmaceutical …
www.who.int71 Introduction and scope of document Pharmaceutical microbiology laboratories may be involved in: — sterility testing; — detection, isolation, enumeration and identifi cation of microorganisms
LABORATORY BIOSAFETY MANUAL - WHO
www.who.intinterim guidelines WHO/CDS/CSR/LYO/2003.4 LABORATORY BIOSAFETY MANUAL SECOND EDITION (REVISED) WORLD HEALTH ORGANIZATION Geneva 2003
Mycobacteriology Laboratory Manual - WHO
www.who.intMycobacteriology Laboratory Manual ii Edita Pimkina, Infectious Diseases and Tuberculosis Hospital Affi liate of Public institution …
Laboratory Guidelines for enumerating CD4 T …
www.who.intSEA-HLM-392 Distribution: Limited Laboratory Guidelines for enumerating CD4 T Lymphocytes in the context of HIV/AIDS Regional Office for South-East Asia
Related documents
The IPEC - Europe Good Distribution Practices Audit Guideline
ipec-europe.orgCopyright © 2011 The International Pharmaceutical Excipients Council - Europe Page 3 IV. Acknowledgements The GDP Committee of the International Pharmaceutical ...
Q7 Q&A - good manufacturing practice for active ...
www.ema.europa.euICH would like to acknowledge the work undertaken by the Pharmaceutical Inspection Co- operation Scheme (PIC/S). PIC/S contributed to this document by selecting and reviewing relevant Q&As that
Q7 Implementation Working Group ICH Q7 Guideline: Good ...
www.ich.orgInternational Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use ICH Secretariat, Chemin des Mines 9, P.O. Box 195, 1211 Geneva 20, Switzerland
ICH HARMONISED TRIPARTITE GUIDELINE
www.ich.orgGOOD MANUFACTURING PRACTICE GUIDE FOR ACTIVE PHARMACEUTICAL INGREDIENTS ICH Harmonised Tripartite Guideline Having reached Step 4 of the ICH Process at the ICH Steering Committee meeting on 10 November 2000, this guideline is recommended for adoption to the three regulatory parties to ICH
ORGANIC SOLVENTS IN THE PHARMACEUTICAL INDUSTRY - …
www.ptfarm.plOrganic solvents in the pharmaceutical industry 5 tical form, some elemental stages have to be per-formed: (a) synthesis of an Active Pharmaceutical
GUIDELINE TO THE INSPECTION OF HORMONE PRODUCT ...
www.who.intWorking document QAS/08.256 February 2008 RESTRICTED GUIDELINE TO THE INSPECTION OF HORMONE PRODUCT MANUFACTURING FACILITIES Please address comments on this proposal, by 13 May 2008, to Dr S. Kopp,