Health Legislation

This Regulation is to determine the fee payable for registration and license of food, medicine, health professional and health institutions.

The Decree establishes the rules for implementing Law 34/2014, of December 31, on the Right to Information. It is applicable to the bodies and institutions of the State, direct and indirect administration, representation abroad, local authorities and also to private entities which, under the Law or by contract, carry out activities of public interest or which, in their activity, benefit from public resources from any source and have in their possession information of public interest.

This document establishes the National List of Essential Medicines for Paediatrics to enable the availability, accessibility and affordability of quality and safe health products and ensure their rational use.

This document establishes the National Essential Medicine List for Adults to enable the availability, accessibility and affordability of quality and safe health products and ensure their rational use.

This Act harmonizes and consolidates the law on registration of persons; provides for registration of individuals; establishes a national identification register; establishes a national registration and identification authority; provides for the issue of national identification cards and aliens identification cards and for related matters.

The document provides the 7th version of the essential medicines list and standard treatment guidelines for Zimbabwe.

This decree creates the National Identification Card for Cape Verdean citizens and establishes the framework for its issue, replacement, use and cancellation.

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.

The purpose of this law is to protect the rights of individuals in the processing of personal data.

The decree creates a multi-sectoral committee to combat counterfeiting and the illicit sale of medicines and other pharmaceutical products, reporting to Niger's Minister of Public Health.

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.

The objective of the law is to govern personal data protection.

This Act makes provisions for the establishment of the Kenya Medical Supplies Authority and for connected purposes.

The order creates a framework for reflection and exchange between players and partners in the implementation of health research, called the "Cadre de Concertation de la Recherche en Santé" (Health Research Consultation Framework), reporting to the Minister in charge of Public Health. Its mission is to promote exchanges and build the capacities of players involved in health research.

The decree establishes a Committee of Experts in charge of technical evaluation, whose mission is to carry out the technical evaluation of applications for registration of pharmaceutical products for human use. It also gives an opinion on the quality, safety and efficacy of pharmaceutical products for human use submitted for registration.

The decree creates the Commission Nationale du Médicament (CNM) for human use, whose mission is to validate the work of the Expert Committee responsible for the technical evaluation of applications for marketing authorization for pharmaceutical products for human use. It also gives a final opinion on marketing authorization applications; applications for renewal, extension of variation and transfer of marketing authorization; temporary suspension of marketing authorization; and proposals for definitive withdrawal of marketing authorization.

The Act promotes the protection of personal information processed by public and private bodies; introduces certain conditions so as to establish minimum requirements for the processing of personal information; provides for the establishment of an Information Regulator to exercise certain powers and to perform certain duties and functions in terms of this Act and the Promotion of Access to Information Act, 2000; provides for the issuing of codes of conduct; provides for the rights of persons regarding unsolicited electronic communications and automated decision making; etc.