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Medicinal Products Lifecycle
  1. Discovery
  2. Preclinical
  3. Clinical
  4. Dossier
  5. Authorities
  6. Approval
  7. Manufacturing
    Quality regulations
  8. Export & Import
  9. Pricing & Reimburcement
  10. Marketing
  11. Postmarketing
  12. Reevaluation & Reexamination
Medical Devices
Japan Monitor (ISSN 1550-3429)
Information Meetings
Legislation and Agreements
All in Japan (ISSN 1550-3402)
E-health Japan (ISSN 1550-3410)
EU Pharma & Medical Devices
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Standards for QA for Drugs, Quasi-drugs, Cosmetics and Medical Devices (Single User License)

 
Standards for QA for Drugs, Quasi-drugs, Cosmetics and Medical Devices (Single User License)Quantity in Basket:none
Code: 7_D_B003
Price:$275.00

 
 
 
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20-page Medicinal Products Lifecycle document. Single user license. Full text in English of the MHLW Ministerial Ordinance on Standards for Quality Assurance for Drugs, Quasi-drugs, Cosmetics and Medical Devices, MHLW Ordinance No. 136, September 22, 2004 (also known as the Good Quality Practice Ordinance" or shortly as the GQP Ordinance". Formatted, indexed, annotated and hyperlinked. Jouhou Koukai Publishing is a Jouhou Koukai business: pharmaceuticals, medical devices, drug approval, regulations, clinical trials, Japan pharmaceutical affairs, and global and Japanese regulatory affairs. Retrieval and consulting on drug approval and technical documents disclosed in Japan. (ISSN 1550-3437) Copyright JKS LLC 2006.


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