WHO requirements for pharma lab

:: Themes & MeSH Subjects
· Themes > English documents > 6. Quality Assurance and Drug Safety
· MeSH > Health Care Economics and Organizations > Social Control, Formal > Legislation > Legislation, Drug
· MeSH > Health Care Quality, Access, and Evaluation > Quality Assurance, Health Care > Guidelines
· MeSH > Health Services Administration > Quality of Health Care > Quality Assurance, Health Care > Guidelines
· MeSH > Natural Sciences > Weights and Measures > Reference Standards
· MeSH > Social Sciences > Sociology > Social Control, Formal > Legislation, Drug
· MeSH > Technology, Industry, and Agriculture > Technology > Quality ControlWHO Expert Committee on Specifications for Pharmaceutical Preparations - WHO Technical Report Series, No. 902 - Thirty-sixth Report(WHO; 2002; 219 pages)

Annex 3 - Good practices for national pharmaceutical control laboratories

General considerations

Glossary

Part One. Management and infrastructure

Part Two. Materials and setting-up of equipment, instruments and other devices

Part Three. Working procedures

Part Four. Safety

References

Appendix 1 - Model analytical test report for active pharmaceutical ingredients, excipients and pharmaceutical products

Appendix 2 - Equipment for a first-stage and medium-size pharmaceutical control laboratory

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