12. Resources (listed in descending order of precedence)
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12. Resources (listed in descending order of precedence)

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Article summary

  1. Ministry of Health, Labour and Welfare of Japan (MHLW)(n.d.) Home Page, MHLW.
  2. Pharmaceuticals and Medical Devices Agency (PMDA)(n.d.) Home PagePMDA.
  3. Hourei (4 December 2019) Clinical Research Method, Hourei (Japanese Ethics Committee).
  4. Cartagena Protocol (29 January 2000) Cartagena Protocol on Biosafety to the convention on Biological Diversity.
  5. Baker Mckenzie (n.d.) Clinical Trials Handbook Asia Pacific, Baker McKenzie.
  6. Japan Registry of Clinical Trials (JRCT), Home PageJRCT.
  7. Ordinance of the Ministry of Health, Labour and Welfare (2022) ‘Ministerial Ordinance on Good Clinical Practice for Drugs’, No. 84. 
  8. Crescent (n.d.) For Companies.
  9. Credevo (16 August 2021) Japan – Clinical Trial Regulatory Process, Credevo.
  10. Coos A (5 April 2022) Data Protection in Japan: All You Need to Know about APPI, Endpoint Protector.

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