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.

For further information, kindly contact GMP Section via email: This email address is being protected from spambots. You need JavaScript enabled to view it. or telephone: 03-78835491

National Pharmaceutical Regulatory Agency (NPRA)
Lot 36, Jalan Universiti (Jalan Profesor Diraja Ungku Aziz), 46200 Petaling Jaya, Selangor, Malaysia.
  • Email:
  • Phone: +603-7883 5400
  • Fax: +603-7956 2924, +603-7956 7075


The Government of Malaysia and the National Pharmaceutical Regulatory Agency are not responsible for any loss or damage caused by the usage of any information obtained from this website.

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