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Pharmaceutical Process Validation (Drugs and the Pharmaceutical Sciences)
  
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Pharmaceutical Process Validation (Drugs and the Pharmaceutical Sciences) (Hardcover)

by Bernard T. Loftus (Contributor, Editor), Robert A. Nash (Editor) "Bernard T. Loftus was director of drug manufacturing in the Food and Drug Administration (FDA) in the 1970s, when the concept of process validation was..." (more)
Key Phrases: project validation plan, multipoint dissolution profile, changeover situations, New York, Pharm Tech, United States (more...)
5.0 out of 5 stars  (1 customer review)

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Editorial Reviews
Book Description
Banner Pharmacaps, Elizabeth, New Jersey. Drugs and the Pharmaceutical Sciences, Volume 57. New edition of a text for pharmaceutical researchers and manufacturers on good manufacturing practice and the applicability of process validation. 31 U.S. contributors. DNLM: Drug Evaluation standards - United States. --This text refers to an out of print or unavailable edition of this title.

Book Info
Stevens Institute of Technology, Hoboken, NJ. Details strategies to establish appropriate validation protocols and conduct process validation assignments, monitor and test specific manufacturing processes for compliance with design limits, and more. --This text refers to the Hardcover edition.
Product Details
  • Hardcover: 286 pages
  • Publisher: Marcel Dekker Inc (April 1984)
  • Language: English
  • ISBN-10: 0824771648
  • ISBN-13: 978-0824771645
  • Average Customer Review: 5.0 out of 5 stars  (1 customer review)
  • Amazon.com Sales Rank: #3,367,497 in Books (See Bestsellers in Books)
    (Publishers and authors: Improve Your Sales)
  • In-Print Editions: Hardcover (3) |  All Editions

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