Environmental Monitoring for Cleanrooms and Controlled Environments
Anne Marie Dixon
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Generic Drug Product Development : Bioequivalence Issues
Isadore Kanfer
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Generic Drug Product Development : International Regulatory Requirements for Bioequivalence
Isadore Kanfer
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Generic Drug Product Development : Specialty Dosage Forms
Leon Shargel
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Pharmaceutical Dosage Forms - Tablets : Unit Operations and Mechanical Properties
Larry L. Augsburger
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Pharmaceutical Dosage Forms - Tablets : Rational Design and Formulation
Larry L. Augsburger
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Pharmaceutical Dosage Forms - Tablets : Manufacture and Process Control
Larry L. Augsburger
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Endotoxins : Pyrogens, LAL Testing and Depyrogenation
Kevin L. Williams
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Producing Biomolecular Substances with Fermenters, Bioreactors, and Biomolecular Synthesizers
William L. Hochfeld
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Microbiological Contamination Control in Pharmaceutical Clean Rooms
Nigel Halls
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Sterile Product Facility Design and Project Management
Jeffrey N. Odum
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Interpharm Master Keyword Guide : 21 CFR Regulations of the Food and Drug Administration, 2002-2003 Edition
Interpharm
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Validated Cleaning Technologies for Pharmaceutical Manufacturing
Destin A. LeBlanc
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Outsourcing in Clinical Drug Development
Roy Drucker
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Sterile Filtration : A Practical Approach
Maik W. Jornitz
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FDA Administrative Enforcement Manual
Florence R. Parker
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Modified-Release Drug Delivery Technology : Volume 1
Michael Rathbone
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Modified-Release Drug Delivery Technology : Volume 2
Michael J. Rathbone
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Fate of Pharmaceuticals in the Environment and in Water Treatment Systems
Diana S. Aga
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Pharmaceutical and Medical Device Validation by Experimental Design
Lynn D Torbeck
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High-Throughput Analysis in the Pharmaceutical Industry
Perry G. Wang
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GMP/ISO Quality Audit Manual for Healthcare Manufacturers and Their Suppliers, (Volume 1 - With Checklists and Software Package)
Leonard Steinborn
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The Pharmaceutical Regulatory Process
Ira R. Berry
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