WHO Expert Committee on specifications for pharmaceutical preparations : forty-first report
Material type:
TextSeries: WHO Technical Report SeriesPublication details: Geneva : World Health Organization, c2007Description: iii, 156 pages : 24 cmISBN: 9789241209434Subject(s): DRUGS QUALITY CONTROL | DRUGS STANDARDLOC classification: RS 51 .W67 2007
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LRC - Main | National University - Manila | Pharmacy | General Circulation | GC RS 51 .W67 2007 (Browse shelf (Opens below)) | c.1 | Available | NULIB000009475 |
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| GC RS 431.P38 .P47 1991 Peptide and protein drug delivery / | GC RS 455 .N37 2010 Textbook of forensic pharmacy / | GC RS 51 .W67 2006 WHO Expert Committee on specifications for pharmaceutical preparations : fortieth report | GC RS 51 .W67 2007 WHO Expert Committee on specifications for pharmaceutical preparations : forty-first report | GC RS 51 .W67 2010 WHO Expert Committee on specifications for pharmaceutical preparations : forty-fourth report | GC RS 51 .W67 2011 WHO Expert Committee on specializations for pharmaceutical preparations : forty-fifth report | GC RS 56 .B43 2012 Communication skills in pharmacy practice : a practical guide for students and practitioners / |
Includes bibliographical references.
Introduction -- General Policy -- Quality control- specifications and tests -- Quality control- International Reference Materials -- Quality control- national laboratories -- Quality assurance- Good Manufacturing practices -- Quality assurance- inspection -- Quality assurance- distribution and trade related -- Quality assurance- risk analysis -- Quality assurance- Stability -- Prequalification -- Regulatory guidance -- Nomenclature and computerized systems -- Miscellaneous -- Summary and recommendations
This report includes the following guidelines of direct relevance to the United Nations Prequalification Programme for Priority Essential Medicines and for quality control laboratories: procedures governing the assessment of pharmaceutical products for procurement by United Nations agencies and for assessing the acceptability of quality control laboratories for use by United Nations agencies, as well as guidance on variations to a prequalified product dossier.
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