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1 Pharmaceutical Inspection Convention
Medicine: PICУниверсальный русско-английский словарь > Pharmaceutical Inspection Convention
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2 Конвенция по фармацевтическим инспекциям
Pharmacology: PIC (Pharmaceutical Inspection Convention), Pharmaceutical Inspection ConventionУниверсальный русско-английский словарь > Конвенция по фармацевтическим инспекциям
См. также в других словарях:
Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme — The Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co operation Scheme (PIC/S) are two international instruments between countries and pharmaceutical inspection authorities. The PIC/S is meant as an instrument to improve co… … Wikipedia
Pharmaceutical Research and Manufacturers of America — (PhRMA) is an industry trade group representing the pharmaceutical research and biotechnology companies in the United States. PhRMA s mission is advocacy for public policies that encourage the discovery of new medicines for patients by… … Wikipedia
Chemical Weapons Convention — Convention on the Prohibition of the Development, Production, Stockpiling and Use of Chemical Weapons and on their Destruction Drafted September 3, 1992[1] Signed January 13, 1993[1] Location Paris and New York[ … Wikipedia
Al-Shifa pharmaceutical factory — The Al Shifa (Arabic for healing ) pharmaceutical factory in Khartoum North, Sudan was constructed between 1992 and 1996 with components imported from the United States, Sweden, Italy, Switzerland, Germany, India, and Thailand. The industrial… … Wikipedia
Biological Weapons Convention — ▪ international agreement formally, Convention on the Prohibition of the Development, Production and Stockpiling of Bacteriological (Biological) and Toxin Weapons and on Their Destruction international treaty that bans the use of… … Universalium
Validation (drug manufacture) — Within the highly regulated environment for development and manufacturing of Pharmaceutical Drugs and medical devices there is a requirement within the regulations to provide an appropriate amount of assurance that critical processes in producing … Wikipedia
Good manufacturing practice — or GMP are practices and the systems required to be adapted in pharmaceutical manufacturing, quality control, quality system covering the manufacture and testing of pharmaceuticals or drugs including active pharmaceutical ingredients, diagnostics … Wikipedia
Good Automated Manufacturing Practice — (GAMP) is a technical sub committee, known as a COP (Community Of Practice) of the International Society for Pharmaceutical Engineering (ISPE). The goal of the community is to promote the understanding of the regulation and use of automated… … Wikipedia
Qualified Person — (QP) is a technical term used in European Union pharmaceutical regulation (Directive 2001/83/EC for Medicinal products for human use). The regulations specify that no batch of medicinal product can be released for sale or supply prior to… … Wikipedia
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Good Engineering Practice — or GEP is applied to engineering and technical activities to ensure that a company manufactures products of the required quality as expected by the Regulatory Authorities. Good Engineering Practices are to ensure that the engineering or software… … Wikipedia