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Guidance Document for Preparation of Good Manufacturing Practice (GMP) Inspections on Traditional Medicines, Health Supplements and Cosmetics Manufacturers
Local Title:
Guidance Document for Preparation of Good Manufacturing Practice (GMP) Inspections on Traditional Medicines, Health Supplements and Cosmetics Manufacturers
Country/Region:
Malaysia
Competent Authority:
National Pharmaceutical Regulatory Agency
Type:
Regulation
Status:
Invalid
Release Date:
2020-07-01
Implementation Date:
2020-07-01
Document
Language Source Title Access
EN
 Official Guidance Document for Preparation of Good Manufacturing Practice (GMP) Inspections on Traditional Medicines, Health Supplements and Cosmetics Manufacturers
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Summary

On July 1, 2020 Malaysia NPRA implemented this guidance document which specifies the requirements and procedures for new cosmetic local manufacturers to apply for a pre-licensing, initial inspection or pre-approval inspection for existing manufacturers.

Main Content

  • Introduction

  • Purpose & Scope

  • Guidelines Used

  • Objective of Pre-licensing/Initial Inspection/Pre-approval Inspection

  • Regulatory Process Description

  • Rejection, Termination or Withdrawal of Inspection

  • Other Information

  • Abbreviations

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