Cosmetic Compliance
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Guidance Document for Preparation of Good Manufacturing Practice (GMP) Inspections on Traditional Medicines, Health Supplements and Cosmetics Manufacturers
Local Title:
GARIS PANDUAN PERSEDIAAN PEMERIKSAAN AMALAN PERKILANGAN BAIK (APB) BAGI PENGILANG TRADISIONAL, SUPLEMEN KESIHATAN DAN KOSMETIK
Country/Region:
Malaysia
Competent Authority:
National Pharmaceutical Regulatory Agency
Type:
Regulation
Status:
In force
Release Date:
2024-05-31
Implementation Date:
2024-06-01
Document
Language Source Title Access
MS
Official Guidance Document for Preparation of GMP Inspections on Traditional Medicines, Health Supplements and Cosmetics Manufacturers-Malaysia
EN
Official Guidance Document for Preparation of GMP Inspections on Traditional Medicines, Health Supplements and Cosmetics Manufacturers English
Summary

On May 31, 2024, NPRA released an updated June 2024 version of the Guidance Document for Preparation of GMP Inspections on Traditional Medicines, Health Supplements and Cosmetics Manufacturers, superseding the previous 2021 edition.

Main Content

  • Introduction

  • Purpose

  • Scope

  • Regulatory Process Description

  • Rejection, Termination or Withdrawal of Inspection

  • Other Information

  • Abbreviations

  • References

  • Appendix 1: Pre-inspection Checklist: Initial / Pre-licensing / Pre-approval Inspection

History
2024-05-31
Guidance Document for Preparation of Good Manufacturing Practice (GMP) Inspections on Traditional Medicines, Health Supplements and Cosmetics Manufacturers
In force
Release Date: 2024-05-31
Implementation Date : 2024-06-01
2021-08-04
2020-07-01
Noteworthy Information
User Guide