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 Profesor Diraja Ungku Aziz), 46200 Petaling Jaya, Selangor, Malaysia.
  • Email: npra@npra.gov.my
  • Phone: +603-7883 5400
  • Fax: +603-7956 2924, +603-7956 7075

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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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  • Last Modified: Friday 12 August 2022, 15:12:42.
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