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Aspects of the Validation of Analytical Methods
🇺🇸 United States
Aspects of the Validation of Analytical Methods
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Computer Systems Validation for the Pharmaceutical and Medical Device Industries
🇺🇸 United States
Computer Systems Validation for the Pharmaceutical and Medi…
By: Richard Chamberlain
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Isolator Technology: Applications in the Pharmaceutical and Biotechnology Industries
🇺🇸 United States
Isolator Technology: Applications in the Pharmaceutical and…
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British Pharmacopoeia 1993
🇺🇸 United States
British Pharmacopoeia 1993
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Guidelines for Drug Master Files (Udsmf)
🇺🇸 United States
Guidelines for Drug Master Files (Udsmf)
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Implementing International Good Practices: Gaps, Gcps, Glps, Gmps
🇺🇸 United States
Implementing International Good Practices: Gaps, Gcps, Glps…
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Fluid Sterilization by Filtration
🇺🇸 United States
Fluid Sterilization by Filtration
By: Peter R. Johnston
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Good Manufacturing Practice Philosophy and Applications
🇺🇸 United States
Good Manufacturing Practice Philosophy and Applications
By: John R. Sharp
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Clinical Research Monitor Handbook: Gcp Tools and Techniques (Practical Clinical Trials Series)
🇺🇸 United States
Clinical Research Monitor Handbook: Gcp Tools and Technique…
By: Deborah Rosenbaum, Fred Smith
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Encyclopedia of Cleanrooms, Bio-Cleanrooms, and Aseptic Areas
🇺🇸 United States
Encyclopedia of Cleanrooms, Bio-Cleanrooms, and Aseptic Are…
By: Philip R. Austin
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Clinical Research Coordinator Handbook: Gcp Tools and Techniques (Practical clinical trials series)
🇺🇸 United States
Clinical Research Coordinator Handbook: Gcp Tools and Techn…
By: Deborah Rosenbaum, Michelle Dresser
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Aspects of Validation of Analytical Methods
🇺🇸 United States
Aspects of Validation of Analytical Methods
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Din Catalog
🇺🇸 United States
Din Catalog
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Guide to Inspections of Dosage Form Drug Manufacturers (Fda Inspection Guidelines)
🇺🇸 United States
Guide to Inspections of Dosage Form Drug Manufacturers (Fda…
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United States: Guideline for Submitting Samples and Analytical Data for Methods Validation (Ref: Daa-Ussadmv)
🇺🇸 United States
United States: Guideline for Submitting Samples and Analyti…
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Pharmaceutical Product Licensing: European Requirements for Registration
🇺🇸 United States
Pharmaceutical Product Licensing: European Requirements for…
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Iso 9004-2 - Quality Management and Quality System Elements - Part 2: Guidelines for Services (1991)
🇺🇸 United States
Iso 9004-2 - Quality Management and Quality System Elements…
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Guide to Inspections of Dosage Form Drug Manufacturers: Cgmps, October 1993 (10/93)
🇺🇸 United States
Guide to Inspections of Dosage Form Drug Manufacturers: Cgm…
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Ec Pharmaceutical Law
🇺🇸 United States
Ec Pharmaceutical Law
By: Peter Bogaert
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