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DRUG REGISTRATION GUIDANCE DOCUMENT (DRGD) - BPFK

DRUG REGISTRATION GUIDANCE DOCUMENT (DRGD) - BPFK

DRUG REGISTRATION GUIDANCE DOCUMENT (DRGD) - BPFK

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Drug Registration Guidance Document (<strong>DRGD</strong>)SECTION E: PARTICULAR OF PRODUCT OWNER, MANUFACTURER,IMPORTER AND OTHER MANUFACTURERPlease select whether the product owner is the product holder, manufacturer orboth product holder and the manufacturer.If the product owner is neither product holder nor the manufacturer, pleaseselect name and address of the product owner (applicable for imported productonly).Other details such as Section E1: Product Owner, Section E2: Manufacturer,Section E3: Repacker, Section E4: Other manufacturer involved in themanufacturing process, Section E5: Store address and Section E6 Importer (Ifany) have to filled. It is mandatory for the Repacker to acquire GMP certificate.SECTION F: SUPPLEMENTARY <strong>DOCUMENT</strong>SLetter of authorization of product ownerThis is applicable for imported product in which the product owner appoints theproduct holder (in Malaysia) as their product holder in MalaysiaLetter of appointment of contract manufacturer and/ or repackerApplicable if the product is contract manufactured by a manufacturer who is not theproduct holder.Letter of acceptance as contract manufacturer and/ or repackerApplicable if the product is contract manufactured by a manufacturer who is not theproduct holder.Certificate Of Pharmaceutical Product (CPP), Free Sale Certificate (CFS) andGood Manufacturing Practice (GMP)CPP can be attached as a replacement of CFS and GMP certificate if the product isclassified as pharmaceutical product in the country of origin:National Pharmaceutical Control Bureau (NPCB)First Edition, January 2013 Page | 215

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