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Short communication: guidelines to good manufacturing practices (g.m.p.) in pharmaceutical manufacturing

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dc.contributor.author R H Shaikh
dc.contributor.author A A Sial
dc.date.accessioned 2023-01-23T08:34:52Z
dc.date.available 2023-01-23T08:34:52Z
dc.date.issued 1995-01-07
dc.identifier.citation Shaikh, R. H., & Sial, A. A. (1995). guidelines to good manufacturing practices (gmp) in pharmaceutical manufacturing. Pakistan Journal of Pharmaceutical Sciences, 8(1), 63-67. en_US
dc.identifier.issn 1011-601X
dc.identifier.uri http://142.54.178.187:9060/xmlui/handle/123456789/16613
dc.description.abstract The object of the GMP and associated rules is the assurance of the quality of the products for the safety, well being and protection of the patient. In achieving this aim it is impossible to over-emphasise the importance of people, at all levels, in the assurance of the quality of medicinal products. The great majority of reported defective medicinal products has resulted from human error or carelessness and not from failure in technology. All the people involved with the production, quality control or distribution of medicinal products, whether key personnel, production or quality control staff, inspectors or other involved in the many activities which lead to a patient taking a medicine, should bear this constantly in mind when performing their duties. en_US
dc.language.iso en en_US
dc.publisher Karachi: Faculty of Pharmacy & Pharmaceutical Sciences University of Karachi en_US
dc.title Short communication: guidelines to good manufacturing practices (g.m.p.) in pharmaceutical manufacturing en_US
dc.type Article en_US


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