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WHO Expert Committee on Specifications for Pharmaceutical Preparations : forty-fifth report.

Contributor(s): World Health Organization | WHO Expert Committee on Specifications for Pharmaceutical Preparations (45th : 2010 : Geneva, Switzerland)Material type: TextTextSeries: Technical report series (World Health Organization) ; 961.Publication details: Geneva, Switzerland : World Health Organization, c2011Description: xii, 428 p. : ill. ; 24 cmISBN: 9789241209618Other title: World Health Organization Expert Committee on Specifications for Pharmaceutical Preparations | Specifications for Pharmaceutical Preparations [Spine title]Subject(s): Drugs -- Standards -- Congresses | Drugs -- Specifications -- Congresses | Drugs -- Quality control -- Congresses | Pharmacopoeias -- Congresses | Drug Industry -- standards -- Congresses | Pharmaceutical Preparations -- standards -- Congresses | Pharmacopoeias as Topic -- Congresses | Reference Standards -- Congresses | Quality Control -- CongressesGenre/Form: Congresses. DDC classification: 615.1 Online resources: Click here to access online Also available via World Wide Web.
Contents:
Introduction -- General policy -- Joint session with the Expert Committee on Biological Standardization -- Quality control: specifications and tests -- Quality control: international reference materials (International Chemical Reference Substances and International Infrared Reference Spectra) -- Quality control: national laboratories -- Quality assurance: good manufacturing practices -- Quality assurance: new approaches -- Quality assurance: distribution and trade of pharmaceuticals -- Prequalification of priority essential medicines -- Prequalification of quality control laboratories -- Prequalification of active pharmaceutical ingredients -- Regulatory guidance -- Nomenclature, terminology and databases -- Summary and recommendations -- Annexes.
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Reports Institute of Development Studies Kolkata
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615.1 W6282w (Browse shelf (Opens below)) Available 5489

The WHO Expert Committee met in Geneva from October 18-22, 2010.

Includes bibliographical references.

Introduction -- General policy -- Joint session with the Expert Committee on Biological Standardization -- Quality control: specifications and tests -- Quality control: international reference materials (International Chemical Reference Substances and International Infrared Reference Spectra) -- Quality control: national laboratories -- Quality assurance: good manufacturing practices -- Quality assurance: new approaches -- Quality assurance: distribution and trade of pharmaceuticals -- Prequalification of priority essential medicines -- Prequalification of quality control laboratories -- Prequalification of active pharmaceutical ingredients -- Regulatory guidance -- Nomenclature, terminology and databases -- Summary and recommendations -- Annexes.

Also available via World Wide Web.

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