These are the guidelines for the registration, renewal, change in characteristics and extension in range of both imported and locally manufactured registered pharmaceutical products.
Clinical Trials Act
This Act regulates the conduct of clinical trials for medicinal products in Mauritius.
The Tanzania Food, Drugs and Cosmetics Act
This Act provides for the efficient and comprehensive regulation and control of food, drugs, medical devices, cosmetics, herbal drugs and poisons and repeals the Food (Control of Quality) Act, 1978, the Pharmaceuticals and Poisons Act, 1978, and provides for related matters.
Dangerous Drug Act
This Act provides for the regulation, control and classification of dangerous drugs.
The Drugs and Prevention of Illicit Traffic in Drugs Act
This Act consolidates the law relating to narcotic drugs, makes provision for the control and regulation of operations relating to narcotic drugs and psychotropic substances; provides for the forfeiture of property derived from or used in illicit traffic in narcotic drugs and psychotropic substances; provides for the prevention of illicit traffic in narcotic drugs and psychotropic substances and implements the provisions of the International Convention on Narcotic Drugs and Psychotropic Substances.
The Medical Stores Department Act
This Act establishes the Medical Stores Department for the procurement, storage and distribution of medical supplies and provides for other matters connected or incidental to the establishment and management of the department.
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.
The Food (Control of Quality) Act
This Act repeals the provisions of the Food and Drugs Ordinance which relates to food; repeals the Meat Hygiene Ordinance, and provides for the more efficient control of the food industry.