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Japan Pharmaceutical Manufacturers

There are six parties directly involved in ICH as well as observers and the International Federation of Pharmaceufical Manufacturers Association (IFPMA see Table 25.1). The six parties are the founder members of ICH, and fhey represenf fhe regulatory bodies and the research-based industry in the European Union (EU), Japan, and the United States in the EU, the European Federation of Pharmaceufical Indusfries and Associations (EFPIA) and the Ministry of Healfh, Labour, and Welfare (MHLW) in Japan, the Japan Pharmaceutical Manufacturers Association (JPMA) and in the United States, the FDA and the Pharmaceutical Researchers and Manufacturers of America (PhRMA). [Pg.476]

Japan Pharmaceutical Manufacturers Association. New Drug Development and Approval Process, http //www.jpma.or.jp/12english/guide industry/new drug/new drug.html [accessed August 8, 2002]. [Pg.277]

Pharmaceutical Administration and Regulation in Japan, March 2004, Japan Pharmaceutical Manufacturers Association. Available at http / /www.jpma. or.jp / 12enghsh / parj / index.html. [Pg.651]

Japan Pharmaceutical Manufacturers Association (JPMA) The key objective of JPMA is the development of a competitive pharmaceutical industry with a greater awareness and understanding of international issues. Over ninety companies are members, including all the major research-based pharmaceutical manufacturers in Japan. ICH work is coordinated through specialized committees of industry experts. JPMA promotes and encourages the adoption of international standards by its member companies. [Pg.92]

One of the key elements for its success is most probably the composition of the organization. It was founded in 1990 as a joint regulatory/industry initiative. The six cosponsors are the EC and the EFPIA (European Federation of Pharmaceutical Industries Association) for the EU, the MHLW and JPMA (Japan Pharmaceutical Manufacturers Association) for Japan, and the U.S. FDA and PhRMA (Pharmaceutical Research and Manufacturers of America) for the United States. [Pg.863]

The Japanese Ministry of Health, Labour and Welfare, and the Japan Pharmaceutical Manufacturers Association. [Pg.17]

Japan Pharmaceutical Manufacturers Association (JPMA) JPMA represents 90 member companies. Membership includes all the major research-based pharmaceutical manufacturers in Japan. [Pg.2913]

The ICH Committee consists of the European Commission of the European Union (EU), the European Federation of Pharmaceutical Industries and Associations (EFPIA), the Ministry of Health and Welfare, Japan (MHW), the Japan Pharmaceutical Manufacturers Association (JPMA), the U.S. [Pg.120]

Japan Pharmaceutical Manufacturers Association (JPMA) established the self-regulatory code Code of Practices for Promotion of Ethical Drugs in 1993. [Pg.21]

Japan Japan Pharmaceutical Manufacturers Association Torii Nihonbashi Building 3-4-1 Nihonbashi-Honcho Chuo-Ku Tokyo 103-0023 Japan Tel 00 81 03 3241 0326 Fax 00 81 03 3242 1767 ... [Pg.207]

Japan Pharmaceutical Manufacturers Association. Promotion Code for Prescription Drugs, April 2004 (www.jpma.or.jp/english/isuues/index.html). [Pg.210]

Japan Pharmaceutical Manufacturers Association, Data Book 1990 (Tokyo, Japan Japan PharmaceuticalManufacturers Association, 1990)... [Pg.332]

Japan Pharmaceutical Manufacturers Association marketing authorization apphcation... [Pg.1672]

JPMA. 1993. Issues associated with laboratory tests in toxicology studies for 1991-1992, pp. 44-46. Japan Pharmaceutical Manufacturers Association. Drug Evaluation Committee, Basic Research Group. [Pg.308]

The six parties that are the founding members of ICH and directly involved in the decision-making process represent the regulatory bodies and the research-based industry in the European Union, Japan, and the USA, the three regions where the majority of new drugs are developed. They are the Committee for Proprietary Medicinal Products of the European Agency for the Evaluation of Medicinal Products and the European Federation of Pharmaceutical Industries and Associations in the EU, the Ministry of Health, Labour and Welfare and Japan Pharmaceutical Manufacturers Association in Japan, the Food and Drug Administration and Pharmaceutical Research and Manufacturers of America in the USA. [Pg.3625]

The ICH committee consists of six members the European Commission of the European Union (EU), the European Federation of Pharmaceutical Industries and Associations (EFPIA), the Ministry of Health and Welfare, Japan (MHW), the Japan Pharmaceutical Manufacturers Association (JPMA), the US. Food and Drug Administration (FDA), and the Pharmaceutical Research and Manufacturers of America (PhRMA). Additional members include observers from the World Health Organization (WHO), European Free Trade Association, and Canada (Health Canada). The International Federation of Pharmaceutical Manufacturers and Associations (IFPM A) has been closely involved with ICH since its inception. This mixture of governmental agencies and professional representatives is performing an exceptional task developing one set of guidelines for three major markets. [Pg.103]

A project named QT Interval Prolongation Project for Database Construction (QT PRODACT) was organised by pharmaceutical companies belonging to the Japan Pharmaceutical Manufacturers Association (JPMA) and contract laboratories belonging to the Japan Association of Contract Laboratories for Safety Evaluation (JACL). The aim of this project was first to construct a non-clinical database to... [Pg.208]


See other pages where Japan Pharmaceutical Manufacturers is mentioned: [Pg.475]    [Pg.552]    [Pg.134]    [Pg.332]    [Pg.94]    [Pg.2915]    [Pg.157]    [Pg.34]    [Pg.212]    [Pg.638]    [Pg.517]    [Pg.535]    [Pg.1643]    [Pg.1864]    [Pg.333]    [Pg.328]    [Pg.372]    [Pg.131]    [Pg.60]    [Pg.256]   


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