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Pharmaceutical Dosage Forms: Parenteral Medications, Vol. 3, 2E at Meripustak

Pharmaceutical Dosage Forms: Parenteral Medications, Vol. 3, 2E by Kenneth E. Avis Herbert Lieberman Leon Lachman, Taylor & Francis Inc

Books from same Author: Kenneth E. Avis Herbert Lieberman Leon Lachman

Books from same Publisher: Taylor & Francis Inc

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  • General Information  
    Author(s)Kenneth E. Avis Herbert Lieberman Leon Lachman
    PublisherTaylor & Francis Inc
    Edition2nd New edition
    ISBN9780824790202
    Pages592
    BindingHardback
    LanguageEnglish
    Publish YearApril 1993

    Description

    Taylor & Francis Inc Pharmaceutical Dosage Forms: Parenteral Medications, Vol. 3, 2E by Kenneth E. Avis Herbert Lieberman Leon Lachman

    Completely updated and enlarged to three volumes (originally published as two volumes) the Second Edition of Pharmaceutical Dosage Forms: Parenteral Medications examines every important aspect of sterile drug products. This volume (3) offers comprehensive coverage of medical devices quality assurance and regulatory issues.;This in-depth reference and text: discusses regulatory requirements in record-keeping based on the US Food and Drug Administration's (FDA) Current Good Manufacturing Practices; places special emphasis on methods of detecting counting and sizing particles; offers new perspectives on contemporary validation concepts and how they affect the validation process; explains current FDA enforcement activities the voluntary compliance policy select court cases and how these relate to parenterals; provides recent materials on the use of audits as a means of verifying the efficacy of manufacturing control systems; highlights new US regulations for medical devices; and examines quality assurance including new information on biological control tests for medical device materials.;With the contributions of leading experts volume 3 of Pharmaceutical Dosage Forms: Parenteral Medications is intended as a day-to-day reference for pharmacists medical device manufacturers quality control and regulatory personnel chemists and drug patent and litigation attorneys as well as a text for upper-level undergraduate graduate and continuing-education students in the pharmaceutical sciences.



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