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  2. Japanese Adverse Drug Event Report database - Wikipedia

    en.wikipedia.org/wiki/Japanese_Adverse_Drug...

    The Japanese Adverse Drug Event Report (JADER) database is a spontaneous reporting system of drug adverse events which is managed by the Pharmaceuticals and Medical Devices Agency (PMDA) in Japan. [1] It has been available since 2012. [1]

  3. Pharmaceuticals and Medical Devices Agency - Wikipedia

    en.wikipedia.org/wiki/Pharmaceuticals_and...

    The Pharmaceuticals and Medical Devices Agency (独立行政法人医薬品医療機器総合機構, Dokuritsu-gyōsei hōjin iyakuhin-iryō-kiki-sōgō-kikō) (PhMDA ...

  4. Sakigake (drug designation) - Wikipedia

    en.wikipedia.org/wiki/Sakigake_(drug_designation)

    Sakigake (さきがけ, lit. "pathfinder", "harbinger") is a drug designation by the Pharmaceuticals and Medical Devices Agency, the pharmaceuticals regulator of Japan.It was designed to provide easier access to novel advanced treatments. [1]

  5. List of stringent regulatory authorities - Wikipedia

    en.wikipedia.org/wiki/List_of_stringent...

    A stringent regulatory authority is a regulatory authority which is: a) a member of the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), being the European Commission, the US Food and Drug Administration and the Ministry of Health, Labour and Welfare of Japan also represented by the Pharmaceuticals and Medical Devices Agency (as before ...

  6. PMDA - Wikipedia

    en.wikipedia.org/wiki/PMDA

    PMDA may refer to: Pharmaceuticals and Medical Devices Agency, a Japanese governmental organization, similar in function to the Food and Drug Administration (FDA) in the US; Plutonium Management and Disposition Agreement, an agreement between the United States and Russia signed in 2000; Pyromellitic dianhydride, an organic compound (an ...

  7. Act on Securing Quality, Efficacy and Safety of Products ...

    en.wikipedia.org/wiki/Act_on_Securing_Quality...

    This article needs to be updated.The reason given is: there was a significant revision to Japan's Pharmaceuticals and Medical Devices Act (PMD Act) in December 4, 2019 (令和 元 年12月 4日) and certain articles in this revised PMD Act took effect April 1, 2020, September 1, 2020, and August 1, 2021; other articles will take effect Dec. 1, 2022 (see also: https://www.natlawreview.com ...

  8. Japanese Pharmacopoeia - Wikipedia

    en.wikipedia.org/wiki/Japanese_Pharmacopoeia

    The Japanese Pharmacopoeia (Japanese: 日本薬局方, Hepburn: Nihon Yakkyokuhō) is the official pharmacopoeia of Japan.It is published by the Pharmaceuticals and ...

  9. List of academic databases and search engines - Wikipedia

    en.wikipedia.org/wiki/List_of_academic_databases...

    Indian Citation Index (ICI) is a home grown abstracts and citation database, with multidisciplinary objective knowledge contents from about 1000 top Indian scholarly journals. It provides powerful search engine to fulfill search and evaluation purposes for researchers, policy makers, decision makers etc. Subscription ICI [78] IARP ...

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