Health Legislation

This Order articulates the values of the pharmacy profession and expected standards of behaviour of pharmacy professionals to clients and the society. It is designed to guide and support professional practice of all pharmacy professionals.

This regulation is issued to implement the Food Medicine and Health Care Administration and Control Proclamation No 661/2009. and covers among other aspects of food safety and quality which includes manufacturing, storage and transportation among other aspects; sale of alcohol; medicine administration and control which includes manufacturing, registration, storage, transportation, importation ad clinical trials among others; traditional and complementary medicine administration and control; post-marketing surveillance; control of tobacco products and places prohibited for smoking among other aspects.  

The Act regulates the quality and safety of medicines and related products and connected matters.

This Act promotes and protects the health and safety of the general public through safeguarding, maintaining and enforcing the highest standards in the practice of pharmacy.

These Regulations govern the issuance of licenses for the importation, exportation, manufacture, distribution, and retail of drugs, etc.

This Act provides for the registration, regulation of the sale, distribution, importation, exportation, manufacture and dispensing of medicines and related substances, and matters incidental thereto.

This Law determines the organization, functioning and competence of the Council of Pharmacists. The Council shall be responsible for ensuring that the rules, honour and dignity of the pharmacy profession are complied with and ensure the protection of public health. 

This decree, taken in application of the provisions of Law No 20/2005 of January 3, 2006, provides for the reorganization of the National Pharmaceutical Office, abbreviated to OPN.

This order, taken in application of the provisions of order No 001/95 of January 14, 1995, concerning the orientation of health policy in the Gabonese Republic, concerns the organization of the pharmaceutical sector.

The Decree establishes the General Bases of the National Pharmaceutical Policy.

This Law defines the legal provisions relating to medicines, medical devices, other health products and the practice of pharmacy in the Islamic Republic of Mauritania. This Law is published in a collection of other legislative acts and can be found on page 3 of the file.

The Diploma approves the Medicines Registration Manual. The purpose of the Manual is to (a) Standardize the procedures and activities relating to the registration of medicines; (b) Clarify the doubts that professionals have encountered when interpreting the Registration Regulations; (c) Support professionals in the field in carrying out their daily activities in a standardized way; (d) Support applicants in complying with registration and post-registration procedures; (e) to make the registration process an optimized and increasingly swift process. 

The Decree sets out the conditions for manufacturing and importing contraceptive products into Burkina Faso.

This Act amends the Medicines and Related Substances Control Act, 2003, so as to amend and delete certain definitions; provides for a period within which the Council must be appointed; provides for the appointment of chairpersons of committees established by the Council; amends provisions relating to the classification of medicines and other substances as scheduled substances; amends provisions relating to the manufacturing, packing and selling of specified Schedule 3 and specified Schedule 4 substances; deletes references to generic substitutions; substitutes references to Schedule 1, Schedule 2, Schedule 3 or Schedule 4 medicines by references to Schedule 1, Schedule 2, Schedule 3 or Schedule 4 substances; inserts provisions relating to the registration of premises engaged in the manufacturing of medicines; amends provisions relating to offences and penalties; amends provisions relating to the destruction of forfeited medicines, scheduled substances or other things; provides for the making of regulations in relation to medicines; amends provisions relating to the exclusion of medicines from the operation of the Act; amends the transitional provisions; amends provisions relating to the repeal and amendment of certain laws; and provides for matters incidental thereto.

The order N°67 sets the conditions of practice of the profession of retail pharmacist. The text of the order is provided as part of a compendium of pharmaceutical legislation (see pages 6 and 7).

The circular N°12 refers to inspections conducted in retail pharmacies. The text of the circular is provided as part of a compendium of pharmaceutical legislation (see pages 7 to 9).

This decree regulates the marketing authorization, registration, manufacture, import, export, marketing, donations and advertising of medicines for human use.

This law, taken in application of the provisions of articles 47 of the Constitution and 67 of ordinance n°01/95 of January 14, 1995 concerning the orientation of health policy in the Gabonese Republic, establishes and organizes the National Order of Pharmacists of Gabon.

This law, taken in application of the provisions of articles 47 of the Constitution and 67 of Ordinance No 01/95 of January 14, 1995 concerning the orientation of health policy in the Gabonese Republic, establishes and organizes the National Order of Pharmacists of Gabon.

This Act provides for the establishment and constitution of a professional Council for the pharmacy profession; determines the powers, duties and functions of such Council; regulates the registration of pharmacists and persons practising professions allied to the pharmacy profession; specifies the education and training and qualifications of persons practising such professions; prohibits the practising of any such profession without being registered; and provides for matters incidental thereto.