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1 PIC/S
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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
Pharmaceutical industry in the People's Republic of China — The pharmaceutical industry is one of the leading industries in People s Republic of China, covering synthetic chemicals and drugs, prepared Chinese medicines, medical devices, apparatus and instruments, hygiene materials, packing materials, and… … 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
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 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
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
Current Good Manufacturing Practice — Unter GMP (Good Manufacturing Practice, Gute Herstellungspraxis) versteht man Richtlinien zur Qualitätssicherung der Produktionsabläufe und umgebung in der Produktion von Arzneimitteln, Wirkstoffen und Medizinprodukten, aber auch bei Lebens und… … Deutsch Wikipedia
Good Manufacturing Practice — Unter Good Manufacturing Practice (engl., kurz GMP, dt. „Gute Herstellungspraxis“) versteht man Richtlinien zur Qualitätssicherung der Produktionsabläufe und umgebung in der Produktion von Arzneimittel und Wirkstoffen, aber auch bei Lebens und… … Deutsch Wikipedia
List of Statutory Instruments of the United Kingdom, 1996 — This is a complete list of all 2071 Statutory Instruments published in the United Kingdom in the year 1996. NOTOC 1 100* Insurance Companies (Pension Business)(Transitional Provisions) (Amendment) Regulations 1996 S.I. 1996/1 * Sea Fishing… … Wikipedia
