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Hasil Pencarian

Ditemukan 25 dokumen yang sesuai dengan query
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Sampurno, author
Yogyakarta: Gadjah Mada University Press, 2011
615.1 SAM m
Buku Teks  Universitas Indonesia Library
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Welty, Gordon, autor
Quality assurance is necessary to maintain quality and services in the pharmaceutical and life science industries. Quality assurance demonstrates that the logic and practice of problem solving can integrate both program efficacy and regulatory compliance. This title is divided into three parts; the first part discusses the process by which...
Oxford: Woodhead Publishing, 2013
615.19 WEL q
Buku Teks  Universitas Indonesia Library
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Smith, Mickey A., author
Baltimore: The Williams and Wilkins, 1976
615.1 SMI p
Buku Teks  Universitas Indonesia Library
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Toumi, Mondher, author
Boca Raton: CRC Press, 2017
615.106 8 TOU i
Buku Teks  Universitas Indonesia Library
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This book describes the way that pharmaceutical projects and programs are currently managed, and offers views from many highly experienced practitioners from within the industry on future directions for drug program management. The book integrates portfolio, program, and project management processes as fundamental for effective and efficient drug product development....
Hoboken: John Wiley & Sons, 2010
e20394503
eBooks  Universitas Indonesia Library
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This book helps pharmaceutical and medical researchers better understand, design, and manage clinical trials through its industry-specific viewpoint that shows how adaptive research technology and methods benefit the drug industry. It gives readers a practical overview of drug development and advocates adaptive design approaches that allow modifications to on-going trials...
Hoboken, New Jersey: John Wiley & Sons, 2010
e20395050
eBooks  Universitas Indonesia Library
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New York: Informa Healthcare, 2008
615.190 PHA I
Buku Teks  Universitas Indonesia Library
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Explaining the assessment of potential drug compounds, this is an ideal introductory reference for those new to drug discovery. It includes sections on pharmacokinetics and drug metabolism, integration of pharmaceutical development, and predictive safety assessment. Topics include: cost analysis, drug transporters, cytochrome P-450 and drug-drug interactions, plasma protein binding, assessing...
Hoboken: John Wiley & Sons, 2010
e20393919
eBooks  Universitas Indonesia Library
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This book answers the questions about the process and costs of pharmaceutical R & D in a compelling narrative focused on the discovery and development of important new medicines. It gives an insider's account of the pharmaceutical industry drug discovery process, the very real costs of misperceptions about the industry,...
Hoboken, New Jersey: John Wiley & Sons, 2009
e20385357
eBooks  Universitas Indonesia Library
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