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Give and take : developmental foreign aid and the pharmaceutical industry in East Africa
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ISBN: 9780691197852 0691197857 9780691197845 0691197849 Year: 2020 Publisher: Princeton Princeton University Press

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"Give and Take looks at local drug manufacturing in Kenya, Tanzania, and Uganda, from the early 1980s to the present, to understand the impact of foreign aid on industrial development. While foreign aid has been attacked by critics as wasteful, counterproductive, or exploitative, Nitsan Chorev makes a clear case for the effectiveness of what she terms "developmental foreign aid." Against the backdrop of Africa's pursuit of economic self-sufficiency, the battle against AIDS and malaria, and bitter negotiations over affordable drugs, Chorev offers an important corrective to popular views on foreign aid and development. She shows that when foreign aid has provided markets, monitoring, and mentoring, it has supported the emergence and upgrading of local production. In instances where donors were willing to procure local drugs, they created new markets that gave local entrepreneurs an incentive to produce new types of drugs. In turn, when donors enforced exacting standards as a condition to access those markets, they gave these producers an incentive to improve quality standards. And where technical know-how was not readily available and donors provided mentoring, local producers received the guidance necessary for improving production processes. Without losing sight of domestic political-economic conditions, historical legacies, and foreign aid's own internal contradictions, Give and Take presents groundbreaking insights into the conditions under which foreign aid can be effective."--

Good design practices for GMP pharmaceutical facilities
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ISBN: 0824754638 Year: 2005 Publisher: Boca Raton (Fla.) : Taylor & Francis,

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FDA good laboratory practice requirements
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ISBN: 9781000789591 Year: 2023 Publisher: Boca Raton, Florida : CRC Press,

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This all-encompassing volume addresses every critical aspect of Good Laboratory Practice (GLP) regulations and demonstrates effective strategies for implementation in a variety of laboratory settings.


Book
Guidance for industry : formal dispute resolution : scientific and technical issues related to pharmaceutical CGMP.
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Year: 2006 Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research,

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Guidance for industry : Q7A good manufacturing practice guidance for active pharmaceutical ingredients.
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Year: 2001 Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research : Center for Biologics Evaluation and Research,

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Guidance for industry : providing regulatory submissions in electronic format, drug establishment registration and drug listing.
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Year: 2009 Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Office of the Commissioner,

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Guidance for industry : submitting type V drug master files to the Center for Biologics Evaluation and Research.
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Year: 2001 Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research,

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Book
Industrial Hygiene in the Pharmaceutical and Consumer Healthcare Industries
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ISBN: 1000983234 Year: 2024 Publisher: Boca Raton, FL : CRC Press,

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Book
Contract manufacturing of medicines
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ISBN: 9789041126429 Year: 2008 Publisher: The Netherlands : Kluwer law international,

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Book
Examining drug compounding : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Thirteenth Congress, first session, May 23, 2013.
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Year: 2014 Publisher: Washington : U.S. Government Printing Office,

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