Guidance Document For Preparation Of Good Manufacturing Practice (GMP) Inspections On Traditional Medicines, Health Supplements And Cosmetics Manufacturers

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The Guidance Document for Preparation of Good Manufacturing Practice (GMP) Inspections on Traditional Medicines, Health Supplements (TMHS) and Cosmetics Manufacturers has been prepared as a reference for new manufacturers of TMHS and cosmetics products. The document is available for download through the link below:

Click Here

Please be informed that an additional pre-inspection checklist (Appendix 1 in the guidance document) is required to be submitted for all applications for initial, pre-licensing and pre-approval inspections from 1 July 2020.

National Pharmaceutical Regulatory Agency (NPRA)

Lot 36, Jalan Universiti (Jalan Prof Diraja Ungku Aziz), 46200 Petaling Jaya, Selangor, Malaysia.

  • Phone: +603-7883 5400



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  • Last Modified: Rabu 17 April 2024, 14:49:33.
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