This Act provides for the establishment of a Medicines Regulatory Authority; for the registration of medicines and medical devices; for the control of medicines and scheduled substances, and for incidental matters.
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 document provides for standard treatment guidelines and the essential medicines list.
Clinical Trials Act
This Act regulates the conduct of clinical trials for medicinal products in Mauritius.
Dangerous Drug Act
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.