Health Legislation

The document establishes the National List of Essential Medicines and Other Health Products.

These are the guidelines for the registration, renewal, change in characteristics and extension in range of both imported and locally manufactured registered pharmaceutical products.

This Act regulates the conduct of clinical trials for medicinal products in Mauritius.

The purpose of the law is the organization of pharmacy, whether for human or veterinary use.

This Act provides for the regulation, control and classification of dangerous drugs.

This Act regulates the practice of pharmacy in the country, establishes guidelines for the licensing, operation, and conduct of pharmacies, as well as regulates the sale and manufacture of pharmaceutical products.