Transcription of 2015 - JPMA
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2015. INFORMATION ON JAPANESE REGULATORY AFFAIRS. Regulatory Information Task Force Japan Pharmaceutical Manufacturers Association Pharmaceutical Administration and Regulations in Japan Japan Pharmaceutical Manufacturers Association 2015. (Japanese). (English). Pharmaceutical Administration and Regulations in Japan This file contains information concerning pharmaceutical administration, regulations, and new drug development in Japan updated annually by the English RA Information Task Force, International Affairs Committee, Japan Pharmaceutical Manufacturers Association (JPMA). The contents are not abstracts of governmental rules or regulations but concise descriptions of most current practices by regulatory agencies and the industry that the working group complies. The file does not contain anything related to forecasts. The file is available also at the homepage of National Institute of Health Sciences ( ). Japan Pharmaceutical Manufacturers Association Good Manufacturing Practice (GMP) 15.
The Ministry of Health, Labour, and Welfare (MHLW) (Koseirodosho in Japanese) was established by a merger of the Ministry of Health and Welfare (MHW) and the Ministry
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