WHO Expert Committee on specializations for pharmaceutical preparations : fiftieth report / World Health Organization

Material type: Text

TextPublication details: Geneva, Switzerland : World Health Organization, c2016Description: iii, 358 pages ; 24 cmISBN:

9789241209960

Subject(s):

DRUGS STANDARDS

LOC classification:

RS 189 .W67 2016

Contents:

Introduction -- General policy -- Quality control-specifications and tests -- Quality control- international reference materials (International Chemical Reference Substances and Infrared Reference Spectra) -- Quality control national laboratories -- Prequalification of quality control laboratories -- Quality assurance collaboration initiatives -- Quality assurance good manufacturing practices -- Quality assurance-distribution and trade of pharmaceuticals -- Prequalification of priority essential medicines and active pharmaceutical ingredients -- Regulatory guidance -- Nomenclature, terminology and databases -- Summary and recommendations

Summary: The Expert Committee on Specifications for Pharmaceutical Preparations works towards clear, independent, and practical standards and guidelines for the quality assurance of medicines.

Item type:

Books

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Holdings
Item type	Current library	Home library	Collection	Call number	Copy number	Status	Date due	Barcode
Books	National University - Manila	LRC - Main General Circulation	Pharmacy	GC RS 189 .W67 2016 (Browse shelf(Opens below))	c.1	Available		NULIB000013394

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Previous	GC RS 189 .W38 2012 Pharmaceutical analysis : a textbook for pharmacy students and pharmaceutical chemists /	GC RS 189 .W55 1992 Good manufacturing practices for pharmaceuticals : a plan for total quality control /	GC RS 189 .W67 2013 WHO Expert Committee on specifications for pharmaceutical preparations : forty-seventh report /	GC RS 189 .W67 2016 WHO Expert Committee on specializations for pharmaceutical preparations : fiftieth report /	GC RS 192 .B56 2004 Bioavailability and bioequivalence in pharmaceutical technology /	GC RS 192 .L33 2013 Lachman/Lieberman's the theory and practice of industrial pharmacy /	GC RS 192 .R63 2016 The FDA & worldwide current good manufacturing practices and quality system requirements: guidebook for finished pharmaceuticals /	Next

Includes bibliographical references.

The Expert Committee on Specifications for Pharmaceutical Preparations works towards clear, independent, and practical standards and guidelines for the quality assurance of medicines.

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