Pharmacy Enforcement

Application/Return Form for the Authorisation Letter / Pharmacy Enforcement Authority Card / Authorisation Letter to Demand and Inspect of Identity Card

This form is used for the application and return of the Authorisation Letter, Pharmacy Enforcement Authority Card, and the Authorisation Letter to Demand and Inspect of Identity Card.
Complete applications and return forms must be submitted to the Pharmaceutical Enforcement Division, Ministry of Health Malaysia (MOH).

English

Application To Import Unregistered Product For The Purpose of Transit in Malaysia

This applications is for a company who wishes to import unregistered products for the purpose of transit and the product is not for sale in the local market.

Complete application shall be submitted to the Pharmacy Enforcement Division, Ministry of Health.

English

Application Form to Import Test Kit Containing Dangerous Drugs/ Psychotropics Subtances

Application form for Type A Poison Licensee (Wholesale or Wholesale and Retail) to import 'test kit' containing dangerous drugs/ psychotropic subtances.

The complete application must be send to Bahagian Penguatkuasa Farmasi, KKM.

English

Application Form For Exporting Products Containing Dextromethorphan

Application form for Type A Licensee (Wholesale/ Retail & Wholesale) to export products containing Dextromethorphan.

Complete application (including required attachment as listed in application form) must be sent to:

Pharmaceutical Service Division

Ministry of Health Malaysia,

Lot 36, Jalan Universiti,

46350 Petaling Jaya Selangor.

 

English

Guidelines on the Application to Classify New Chemical as Poison under the Poisons Act 1952

These guidelines explain the procedures involved when applying for classification of new chemical as poison under the Poisons Act 1952.

English

A Guide To Legislations on the Recording, Labelling, Storage and Disposal of Poisons and Psychotropic Substances Applicable to Private Clinics

This guideline provides information for the medical practitioners in private clinics/ practice. This guideline contains information about the legal provisions relating to the recording, labelling, storage and disposal of poisons and psychotropic substances.

English

Medicine Advertisements Board

Medicine Advertisements Board (MAB) was established under the provisions of The Medicine Advertisements Board Regulations 1976. The Board was established to discuss the approval for application on medical products or healthcare facilities and services advertisement received and at the discretion, the Board may:
• Issue approval for an advertisement.
• Review, revise its policies and guidelines as necessary
• Cancel / withdraw the approval granted

Membership

Poisons Board

Introduction
 

The Poisons Board is established in pursuant to the provisions under the Poisons Act 1952 and serves to advise the Minister of Health on the followings:
 
•    Classification of new chemicals as Poison
•    Reclassification of poison in the Poisons List
•    Removal of Poison from the Poisons List
•    Amendment of the psychotropic substances list in the Third Schedule

Pharmacy Enforcement Division

Introduction

Dikir Farmasi - Jom Guna Ubat Berdaftar

Terbitan Caw. Penguatkuasa Farmasi Negeri Kelantan

English

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