This Decree approves the amended statutes of the Beninese pharmaceutical regulatory agency, now named “Beninese Agency for Medicines and other Health Products”.
The decree defines the health benefit package of the universal health insurance scheme.
These regulations were developed in the exercise of the powers conferred by sections 24, 30, 46)2), 47(5) and 50(1) of the Social Health Insurance Act, 2023, by the Cabinet Secretary for Health, in consultation with the Board for the Social Health Authority.
This regulation establishes the rules applicable to the exercise of pharmaceutical activity, in the public and private sectors, by natural or legal persons.
This law establishes the rules relating to medicines, other health products and pharmacy.
The Decree establishes the health benefit package covered under the Universal Health Insurance. The decree was published on 25 November 2023 in the Official Journal.
This decree regulates the exercise of hospital pharmaceutical activity in the health structures of the National Health Service. It covers all health structures of the National Health Service that carry out this activity, namely central hospitals and regional hospitals. Its purpose is to organize, improve, optimize and standardize hospital pharmaceutical services in the National Health Service.
The Decree specifies the application of certain provisions of the law establishing the Universal Health Insurance Scheme, such as affiliation and registration, the insured person's card, care benefits covered, the assumption of responsibility for benefits, health care providers, among other aspects.
The Decree sets out the statutes of the Nigerian Pharmaceutical Regulatory Agency.
The law establishes the Pharmacy Council of Nigeria and regulates the standard of training and practice of pharmacy.
This Decree establishes and fixes the rules of organization and operation of the Senegalese Pharmaceutical Regulatory Agency (ARP)
This document provides the benefits package of the National Health Insurance Scheme as offered to its beneficiaries through private health providers.
The law creates the Burundian Authority for the Regulation of Medicines for Human Use and Food. The authority's general aim is to protect public health by promoting the quality and safety of products such as prefabricated and ambient foods, medicines for human use, cosmetics and dietary products containing active ingredients, herbal medicines, traditional medicines, and medical devices, among others.
These Instructions establish the methodology to determine the community-based health insurance benefit package.
This law establishes a universal health insurance in the Togolese Republic.
The legislation regulates the production, import, export, conservation, distribution, quality analysis and sale of medicines for human use, including traditional medicines, as well as all other health products, pharmaceutical practice and opticianry.
Decreto No 115/2020 Aprova o Estatuto Orgânico da Autoridade Nacional Reguladora de Medicamento
The Decree approves the Organic Statute of the Autoridade Nacional Reguladora de Medicamento (The National Medicines Regulatory Authority). The purpose of this Decree is to define the rules governing the organization, management and operation, as well as the powers of its bodies.
This Act establishes the Pharmacy and Medicines Regulatory Authority; provides for the functions and powers of the Authority; and provides for matters connected therewith and incidental thereto.
This Decree creates and establishes the rules for the organization and operation of the National Order of Pharmacists of Mauritania (ONPM). This Decree is published in a collection of other legislative acts and can be found on page 10 of the file.
The law regulates the manufacture and registration of medicines, the approval of medical devices, and sets out rules for pharmacies and the practice of the profession of pharmacist.