Search Results for Pharmaceutical technology -- Quality control.

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Yazar

Kanfer, Isadore.

(2)

LeBlanc, Destin A., author.

(2)

Shargel, Leon, 1941-

(2)

Wiley InterScience (Online service)

(2)

Agalloco, James P., 1948-

(1)

Agalloco, James P., 1948- editor.

(1)

Ball, Douglas J.

(1)

Behme, Stefan, author.

(1)

Carleton, Frederick J., 1925-

(1)

Cloud, Phillip A.

(1)

DeSantis, Phil, editor.

(1)

Dumitriu, Helene I.

(1)

Gad, Shayne C., 1948-

(1)

García-Munoz, Salvador, 1971- editor.

(1)

Grilli, Anthony, editor.

(1)

Haider, Syed Imtiaz, author.

(1)

Haider, Syed Imtiaz., author.

(1)

Hintze, Thomas O.

(1)

(1)

Jiang, Liwen, 1963- editor.

(1)

Kermode, Allison R., editor.

(1)

May, Joan C. (Joan Christine)

(1)

(1)

Norwood, Daniel L.

(1)

Nusim, Stanley.

(1)

Pavell, Anthony, editor.

(1)

Reklaitis, G. V., 1942- editor.

(1)

(1)

Seiberling, Dale A.

(1)

Seymour, Christine, 1967- editor.

(1)

Signore, Andrew A., author.

(1)

Stokes, David., author.

(1)

Stults, Cheryl L.

(1)

Turner, Simon G.

(1)

Wingate, Guy, editor.

(1)

Wrigley, Graham C., author.

(1)

(1)

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Tümünü genişlet

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Pharmaceutical technology -- Quality control.

(15)

Pharmaceutical technology -- Standards.

(4)

(4)

MEDICAL / Pharmacology

(3)

(2)

Drugs -- Law and legislation.

(2)

Electronic books.

(2)

MEDICAL -- Pharmacology.

(2)

Pharmaceutical industry -- Quality control.

(2)

Pharmaceutical industry.

(2)

Pharmaceutical technology -- Automation -- Quality control.

(2)

(2)

Biological laboratories -- Quality control.

(1)

Biological products -- Drying.

(1)

Biotechnology industries -- Standards -- United States.

(1)

(1)

(1)

Computers -- Testing.

(1)

(1)

(1)

Drug Evaluation -- legislation & jurisprudence -- United States.

(1)

(1)

Drug Industry -- legislation & jurisprudence -- United States.

(1)

(1)

Drug delivery systems -- Safety measures.

(1)

Drug development.

(1)

Drug factories.

(1)

Drug stability.

(1)

Drugs -- Design

(1)

Drugs -- Design.

(1)

Drugs -- Dosage forms.

(1)

Drugs -- Drying.

(1)

Drugs -- Law and legislation -- United States -- Handbooks, manuals, etc.

(1)

Drugs -- Quality control.

(1)

Drugs -- Sterilization.

(1)

(1)

(1)

(1)

Industrial & Technical.

(1)

Industrie pharmaceutique.

(1)

Information technology -- Quality control.

(1)

Leachate -- Health aspects.

(1)

(1)

Materia medica, Vegetable

(1)

Materia medica, Vegetable.

(1)

Medical instruments and apparatus industry -- Standards -- United States.

(1)

Medical laboratories -- Quality control.

(1)

Medicine, Botanic

(1)

Medicine, Botanic.

(1)

Molecular Biology.

(1)

Molecular Farming -- methods

(1)

Molecular pharmacology

(1)

Molecular pharmacology.

(1)

Médicaments -- Conception.

(1)

Médicaments protéiques.

(1)

Pharmaceutical chemistry.

(1)

Pharmaceutical industry

(1)

Pharmaceutical industry -- Automation -- Quality control.

(1)

Pharmaceutical industry -- Standards -- United States.

(1)

Pharmaceutical industry -- Standards.

(1)

Pharmaceutical policy.

(1)

Pharmaceutical technology -- Equipment and supplies -- Cleaning.

(1)

Pharmaceutical technology -- Quality control

(1)

Pharmaceutical technology -- Quality control -- Handbooks, manuals, etc.

(1)

Pharmaceutical technology -- Software -- Testing.

(1)

Pharmaceutical technology.

(1)

Pharmacologie moléculaire.

(1)

(1)

Phytothérapie.

(1)

Plant Preparations -- pharmacology

(1)

Plants, Genetically Modified -- growth & development

(1)

Production management.

(1)

(1)

(1)

Quality Control -- United States.

(1)

SCIENCE / Chemistry / General

(1)

(1)

(1)

Tablets (Medicine)

(1)

Techniques pharmaceutiques -- Qualité -- Contrôle.

(1)

(1)

İlaçlar, Jenerik

(1)

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1.

Validation of pharmaceutical processes için kapak resmi

Validation of pharmaceutical processes

Validation of pharmaceutical processes

Yazar

Agalloco, James P., 1948- Carleton, Frederick J., 1925-

Yer Numarası

RS199 .S73 V345 2007

Elektronik Erişim

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2.

Validation standard operating procedures : a step-by-step guide for achieving compliance in the pharmaceutical, medical device, and biotech industries için kapak resmi

Validation standard operating procedures : a step-by-step guide for achieving compliance in the pharmaceutical, medical device, and biotech industries

Validation standard operating procedures : a step-by-step guide for achieving compliance in the pharmaceutical, medical device, and biotech industries

Yazar

Haider, Syed Imtiaz, author.

Yer Numarası

RS192 .H353 2006

Elektronik Erişim

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3.

Good design practices for GMP pharmaceutical facilities için kapak resmi

Good design practices for GMP pharmaceutical facilities

Good design practices for GMP pharmaceutical facilities

Yazar

Signore, Andrew A., author. Jacobs, Terry.

Yer Numarası

RS192 .S54 2005

Elektronik Erişim

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4.

Generic drug product development : solid oral dosage forms için kapak resmi

Generic drug product development : solid oral dosage forms

Generic drug product development : solid oral dosage forms

Yazar

Shargel, Leon, 1941- Kanfer, Isadore.

Yer Numarası

QV 704 D8426 2005

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5.

Pharmaceutical engineering change control için kapak resmi

Pharmaceutical engineering change control

Pharmaceutical engineering change control

Yazar

Turner, Simon G.

Yer Numarası

RS192 .P455 2004

Elektronik Erişim

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6.

Facility validation : theory, practice, and tools için kapak resmi

Facility validation : theory, practice, and tools

Facility validation : theory, practice, and tools

Yazar

Wrigley, Graham C., author.

Yer Numarası

RS192 .W75 2004

Elektronik Erişim

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7.

Testing computer systems for FDA/MHRA compliance için kapak resmi

Testing computer systems for FDA/MHRA compliance

Testing computer systems for FDA/MHRA compliance

Yazar

Stokes, David., author.

Yer Numarası

RS418 .S76 2004

Elektronik Erişim

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8.

Pharmaceutical master validation plan : the ultimate guide to FDA, GMP, and GLP compliance için kapak resmi

Pharmaceutical master validation plan : the ultimate guide to FDA, GMP, and GLP compliance

Pharmaceutical master validation plan : the ultimate guide to FDA, GMP, and GLP compliance

Yazar

Haider, Syed Imtiaz., author.

Yer Numarası

RS192 .H3533 2002

Elektronik Erişim

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9.

Validating corporate computer systems : good IT practice for pharmaceutical manufacturers için kapak resmi

Validating corporate computer systems : good IT practice for pharmaceutical manufacturers

Validating corporate computer systems : good IT practice for pharmaceutical manufacturers

Yazar

Wingate, Guy, editor.

Yer Numarası

RS192 .V35 2000

Elektronik Erişim

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10.

Validated cleaning technologies for pharmaceutical manufacturing için kapak resmi

Validated cleaning technologies for pharmaceutical manufacturing

Validated cleaning technologies for pharmaceutical manufacturing

Yazar

LeBlanc, Destin A., author.

Yer Numarası

RS199 .S73 L43 2000

Elektronik Erişim

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11.

Pharmaceutical equipment validation : the ultimate qualification handbook için kapak resmi

Pharmaceutical equipment validation : the ultimate qualification handbook

Pharmaceutical equipment validation : the ultimate qualification handbook

Yazar

Cloud, Phillip A.

Yer Numarası

RS192 .C57 1998

Elektronik Erişim

Taylor & Francis https://www.taylorfrancis.com/books/9781439805947
Taylor & Francis https://www.taylorfrancis.com/books/9780367802998
OCLC metadata license agreement http://www.oclc.org/content/dam/oclc/forms/terms/vbrl-201703.pdf

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12.

Good drug regulatory practices : a regulatory affairs quality manual için kapak resmi

Good drug regulatory practices : a regulatory affairs quality manual

Good drug regulatory practices : a regulatory affairs quality manual

Yazar

Dumitriu, Helene I. Hintze, Thomas O.

Yer Numarası

RS189 .D86 1997

Elektronik Erişim

Taylor & Francis https://www.taylorfrancis.com/books/9781842145623
Taylor & Francis https://www.taylorfrancis.com/books/9780367805487
OCLC metadata license agreement http://www.oclc.org/content/dam/oclc/forms/terms/vbrl-201703.pdf

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