Public Alert Notice on Counterfeit Drugs

Download a PDF copy of the alert notice as it appeared in the press.

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The Pharmacy and Poisons Act - CAP 244 (PDF)

Advertisement Guidelines and Requirements (MS Word format).

Checklist for submitting documents to the Expert Committee on Clinical Trials (MS Word format).

Application Form for Good Manucaturing Practice Inspection for Pharmaceutical Manufacturing Facilities (MS Word format).

National Pharmacovigilance Guidelines.

Suspected Adverse Drug Reaction Notification Form.

Form for Reporting Poor Quality Medicinal Products.

New Application for Registration of Drug

Drug Registration Guidelines

Guidelines for Product Recall and Product Withdrawal

Guidelines for Good Distribution Practices (GDP) for Pharmaceuticals

Guidelines for Registration of Herbal and Complementary Products