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Ordonnance ministerielle 630-991 portant révision de l'ordonnance ministerielle 630/450/750 portant mode et conditions d'homologation des médicaments à usage humain et autresintrants pharmaceutiques au Burundi
The purpose of this ordinance is to organize the registration of medicines for human use and other pharmaceutical inputs in Burundi.
Règlement No 04/2020/CM/UEMOA relatif aux procédures d’homologation des produits pharmaceutiques à usage humain
The purpose of the Regulation is to define the procedures for approving pharmaceutical products for human use in the member states of the West African Economic and Monetary Union.
Guidelines for Registration of Human Vaccines
These guidelines prescribe data, which is required to be submitted to the National Drug Authority to demonstrate the safety, efficacy and quality of vaccines being applied for market authorization. The guidelines also describe the format (CTD) in which dossiers should be presented in support of the application.
Guidelines for implementing TB-HIV collaborative activities in Kenya
These guidelines provide a comprehensive framework aimed at addressing the dual burden of tuberculosis (TB) and HIV in the country. The guidelines emphasize the importance of integrated service delivery to improve health outcomes for individuals affected by both diseases.
Dangerous Drug Act
This Act provides for the regulation, control and classification of dangerous drugs.
Edgar Laurent Tuberculosis Foundation Act
This Act establishes the Edgar Laurent Tuberculosis Foundation in Mauritius to combat tuberculosis through awareness, prevention, and treatment programs.