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The Theory and Practice of Industrial Pharmacy / Leon Lachman, Herbert A. Lieberman, and Joseph L. Kanig.

By: Contributor(s): Material type: TextTextPublisher: New Delhi : CBS Publishers & Distributors, 2024Edition: 4th editionDescription: 1203 pages : illustrations ; 26 cmContent type:
  • text
Media type:
  • unmediated
Carrier type:
  • volume
ISBN:
  • 9788123922898
Subject(s): DDC classification:
  • 23 615.1 L.L.T
Contents:
Section 1: Principles of Pharmaceutical Processing — Mixing; Milling; Drying; Compression; Emulsion and Suspension; Rheology; Clarification and Filtration. Section 2: Pharmaceutical Dosage Form Design — Preformulation; Biopharmaceutics; Statistical Applications. Section 3: Pharmaceutical Dosage Forms — Tablets; Tablet Coating; Capsules; Sustained‑Release Dosage Forms; Liquids; Pharmaceutical Suspensions; Emulsions; Semisolids; Sterile Products. Section 4: Product Processing, Packaging, Evaluation and Regulations — Pilot Plant Scale‑up; Packaging Material Science; Kinetic Principles and Stability Testing; Quality Control and Assurance; Drug Regulatory Affairs. ([turn0search3])
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Holdings
Item type Current library Call number Copy number Status Date due Barcode Item holds
Books Books Media and mass communication Library W3 615.1 L.L.T C.1 Available MA0002256
Books Books Media and mass communication Library W3 615.1 L.L.T C.2 Available MA0002266
Total holds: 0

Includes bibliographical references and index.

Section 1: Principles of Pharmaceutical Processing — Mixing; Milling; Drying; Compression; Emulsion and Suspension; Rheology; Clarification and Filtration. Section 2: Pharmaceutical Dosage Form Design — Preformulation; Biopharmaceutics; Statistical Applications. Section 3: Pharmaceutical Dosage Forms — Tablets; Tablet Coating; Capsules; Sustained‑Release Dosage Forms; Liquids; Pharmaceutical Suspensions; Emulsions; Semisolids; Sterile Products. Section 4: Product Processing, Packaging, Evaluation and Regulations — Pilot Plant Scale‑up; Packaging Material Science; Kinetic Principles and Stability Testing; Quality Control and Assurance; Drug Regulatory Affairs. ([turn0search3])

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