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Medicinal Products Lifecycle
  1. Discovery
  2. Preclinical
  3. Clinical
  4. Dossier
  5. Authorities
  6. Approval
  7. Manufacturing
  8. Export & Import
  9. Pricing & Reimburcement
  10. Marketing
  11. Postmarketing
  12. Reevaluation & Reexamination
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Medicinal Products Lifecycle 4. Dossier

Specific Q & A On CTD - Quality Guideline for Japanese Submission (Single User License)

 
Specific Q & A On CTD - Quality Guideline for Japanese Submission (Single User License)Quantity in Basket:none
Code: 4_D_K003
Price:$125.00

 
 
 
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28-page document. Detailed answers on CTD - Quality Guideline released by the Japanese regulatory authorities. Formatted, indexed and hyperlinked. Copyright © JKS LLC 2003.


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Type: Key document