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DRUG REGISTRATION GUIDANCE DOCUMENT (DRGD) - BPFK

DRUG REGISTRATION GUIDANCE DOCUMENT (DRGD) - BPFK

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Drug Registration Guidance Document (<strong>DRGD</strong>)Step II:4.5.Letter of Acceptance from Contract Manufacturer(if applicable)Is the active ingredient(s) patented in Malaysia?(Yes/ No)(If yes, please attach the related document)6. Certificate of Pharmaceutical Product (CPP)7. CPP Issuing Body8.Is this product licensed to be placed on the market for use in the exportingcountry? (Yes/ No)(If no, please state the reason)9.Is the product on the market in the exporting country? (Yes/ No)(If no, please state the reason)10. Date of Issue of CPP11. Date of Expiry of CPP12. Certificate of Free Sale (CFS)13. CFS Issuing Body14. Date of Issue of CFS15. Date of Expiry of CFS16. Certificate of Good Manufacturing Practice (GMP)17. Certificate of GMP Issuing Body18. Date of Issue of Certificate of GMP19. Date of Expiry of Certificate of GMP20.Summary of Product Characteristics(Product Data Sheet)21. Patient Information Leaflet (PIL)22. *Attachment of Protocol Analysis23. *Attachment of Analytical Validation24. *Certificate of Analysis (CoA)25. Other Supporting Document (if any)26. Manufacturer (Name and address)National Pharmaceutical Control Bureau (NPCB)First Edition, January 2013 Page | 138

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