Good manufacturing practices for pharmaceuticals : a plan for total quality control / Sidney H. Willig and James R. Stoker
Material type:
TextPublication details: New York : Marcel Dekker, c1992Description: iii, 268 pages : 23 cmISBN: 0824785940Subject(s): PHARMACEUTICAL INDUSTRY -- QUALITY CONTROL | DRUGS -- STANDARDS -- UNITED STATESLOC classification: RS 189 .W55 1992
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LRC - Main | National University - Manila | Pharmacy | General Circulation | GC RS 189 .W55 1992 (Browse shelf (Opens below)) | c.1 | Available | NULIB000004005 |
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| GC RS 189 .H36 2012 c.1 Introduction to pharmaceutical chemical analysis / | GC RS 189 .H36 2012 c.2 Introduction to pharmaceutical chemical analysis / | 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 / |
Includes bibliographical references and index.
Status and Applicability of Regulations: Current Good Manufacturing Practices in Manufacturing, Processing, Packaging, and Holding of Drugs -- Finished Pharmaceuticals: General Provisions (Subpart A) -- Organization and Personnel: (Subpart B) -- Building and Facilities: (Subpart C) -- Equipment: (Subpart D) -- Control of Components and Drug Product Containers and Closures: (Subpart E)
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