Compliance handbook for pharmaceuticals, medical devices, and biologics

著者

    • Medina, Carmen

書誌事項

Compliance handbook for pharmaceuticals, medical devices, and biologics

edited by Carmen Medina

（Drugs and the pharmaceutical sciences, v. 136）

M. Dekker, c2004

大学図書館所蔵 件 / 全2件

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注記

Includes bibliographical references and index

内容説明・目次

内容説明

This text lists the necessary steps for meeting compliance requirements during the drug development process. It presents comprehensive approaches for validating analytical methods for pharmaceutical applications.

目次

  • Regulatory submissions, Patricia Fritz and Anisa Dhalla
  • compliance requirements during the drug development process, Martin D. Hynes
  • validation - a new perspective, James Agalloco
  • validating analytical methods for pharmaceutical applications - a comprehensive approach, Paul A. Winslow and Richard F. Meyer
  • the stability testing programme, Maria Geigel
  • computer validation - a compliance focus, Timothy Horgan and Timothy Carey
  • compliance issues associated with cleaning in the pharmaceutical industry, William E. Hall
  • the batch record - a blueprint for quality and compliance, John Fugate
  • change management - a far reaching, comprehensive and integrated system, Susan Freeman
  • the vendor qualification programme, Eizabeth M. Troll and Karen L. Hughes
  • handling laboratory and manufacturing deviations, Robert B. Kirsch
  • the internal audit programme - a quality assessment, Graham Bunn
  • pre-approval inspections - the critical compliance path to success, Martin D. Hynes
  • international compliance issues and trends, Alan G. Minsk
  • strategic planning for compliance and regulatory defensiveness, Ron Johnson
  • unique and unprecedented compliance challenges in the biologics area, Anne Hoppe and Curtiss Scribner
  • the impact of total quality performance on compliance, Carmen Medina, Judith Beach, Valerie Palumbo and Douglas B. Poucher.

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