Search Results for Pharmaceutical technology -- Quality control.

Regulated bioanalytical laboratories technical and regulatory aspects from global perspectives

2024-11-04T15:22:42Z

Author Zhou, Michael. Wiley InterScience (Online service)
Preferred Shelf Number ONLINE
Electronic Access Click here to view book John Wiley http://dx.doi.org/10.1002/9780470920671 ebrary http://site.ebrary.com/id/10577672
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Leachables and Extractables Handbook Safety Evaluation, Qualification, and Best Practices Applied to Inhalation Drug Products.

2024-11-04T15:22:42Z

Author Ball, Douglas J. Norwood, Daniel L. Stults, Cheryl L. Nagao, Lee.
Preferred Shelf Number ONLINE
Electronic Access Wiley InterScience An electronic book accessible through the World Wide Web; click for information http://public.eblib.com/EBLPublic/PublicView.do?ptiID=818476 Wiley http://onlinelibrary.wiley.com/book/10.1002/9781118147672
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Active pharmaceutical ingredients development, manufacturing, and regulation

2024-11-04T15:22:42Z

Author Nusim, Stanley.
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Electronic Access Distributed by publisher. Purchase or institutional license may be required for access.
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Freeze drying/lyophilization of pharmaceutical and biological products

2024-11-04T15:22:42Z

Author Rey, Louis. May, Joan C. (Joan Christine)
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Clean-in-place for biopharmaceutical processes

2024-11-04T15:22:42Z

Author Seiberling, Dale A.
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Pharmaceutical manufacturing handbook regulations and quality

2024-11-04T15:22:42Z

Author Gad, Shayne C., 1948- Wiley InterScience (Online service)
Preferred Shelf Number ONLINE
Electronic Access Ebook Library http://public.eblib.com/EBLPublic/PublicView.do?ptiID=333795 John Wiley http://dx.doi.org/10.1002/9780470259832
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Validation of pharmaceutical processes

2024-11-04T15:22:42Z

Author Agalloco, James P., 1948- Carleton, Frederick J., 1925-
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Validation standard operating procedures a step-by-step guide for achieving compliance in the pharmaceutical, medical device, and biotech industries

2024-11-04T15:22:42Z

Author Haider, Syed Imtiaz.
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Generic drug product development : solid oral dosage forms

2024-11-04T15:22:42Z

Author Shargel, Leon, 1941- Kanfer, Isadore.
Preferred Shelf Number QV 704 D8426 2005
Format: Books
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Good design practices for GMP pharmaceutical facilities

2024-11-04T15:22:42Z

Author Signore, Andrew A. Jacobs, Terry.
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Testing computer systems for FDA/MHRA compliance

2024-11-04T15:22:42Z

Author Stokes, David.
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Pharmaceutical engineering change control

2024-11-04T15:22:42Z

Author Turner, Simon G.
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Facility validation theory, practice, and tools

2024-11-04T15:22:42Z

Author Wrigley, Graham C.
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Pharmaceutical master validation plan the ultimate guide to FDA, GMP, and GLP compliance

2024-11-04T15:22:42Z

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

2024-11-04T15:22:42Z

Validated cleaning technologies for pharmaceutical manufacturing

2024-11-04T15:22:42Z

Author LeBlanc, Destin A.
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Pharmaceutical equipment validation the ultimate qualification handbook

2024-11-04T15:22:42Z

Author Cloud, Phillip A.
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Good drug regulatory practices a regulatory affairs quality manual

2024-11-04T15:22:42Z

Author Dumitriu, Helene I. Hintze, Thomas O.
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