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  Good Manufacturing Practice/Good Distribution Practice

According to the Control of Drugs and Cosmetics Regulations 1984, complaince to Good Manufacturing Practice is a pre-quisite for the application of a manufacturing license as well as product registration/ cosmetic notification.

Good Manufacturing Practice (GMP) is a standard that should be followed by manufacturers of registered pharmaceutical/ traditional products and notified cosmetics to ensure that the product manufactured is safe, efficious and of quality.

Centre for Compliance and Licensing (CCL) is responsible for the Good Manufacturing Practice (GMP) inspections of manufacturers of registered products and notified cosmetics to ensure manufacturers compliance towards the current GMP requirements. CCL, with the assistance of the State Pharmacy Enforcement Division, is responsible for ensuring the importers and wholesalers of registered products adhere to the current Good Distribution Practice (GDP) requirements.

GMP guidelines are as below:

Guidelines Product Type / Category
PIC/S Guide to Good Manufacturing Practice for Medicinal Products Pharmaceuticals (Poison and Non-Poison) 
Veterinary Products
GMP Guideline for Traditional Medicines & Health Supplements-1st. Ed. 2008. Traditional Products
Health Supplements
Guidelines on Good Manufacturing Practice (GMP) for Cosmetic Cosmetics
Supplementary Guidelines on GMP for Veterinary Premixes, Supplements and Herbal/Natural Preparations, 1st Edition, 1 January 2012 Veterinary Products
Guidelines on Good Distribution Practice (GDP); 1st Edition 2011. For activities related to the storage and distribution by manufacturers, importers and wholesalers (where applicable)

For any further enquiries, please refer to FAQ APB/AEB (GMP/GDP) and GMP Guidelines.

GMP Certificate

GMP certificates are issued for the purpose of exportation of locally manufactured registered products. It endorses that the local manufacturer complies with the current GMP requirements. These certificates are required by the overseas regulatory agencies for products registration in their countries. Thus when filling in the GMP certificate application form, the correct address of overseas regulatory agencies given by the companies is crucial.

For those companies interested to apply GMP certificate, company can download Borang Permohonan Sijil APB (BPFK-420)

 Other News & Important Announcements

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Updated : 14 May 2013




 
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