The Agence Marocaine du Médicament et des Produits de Santé will require a signed commitment declaration from medical representatives, responsible pharmacists and agency heads when processing applications to carry medical samples.
The National Agency for Food and Drug Administration and Control has enrolled six hundred pharmacists from all thirty-six states and the Federal Capital Territory into a volunteer reserve programme to strengthen regulatory presence in communities, markets and health facilities.
Health Minister Ussene Isse has highlighted ANARME’s attainment of WHO Maturity Level 3 as a major advance for medicines regulation in Mozambique, during the 51st Health Coordinating Council in Beira.
The South African Health Products Regulatory Authority hosted Lesotho’s Radiation Protection Agency for knowledge sharing on radiation regulation, quality management and institutional frameworks.
Uganda’s National Drug Authority (NDA) has closed more than 100 illegal drug outlets and impounded medicines worth over sh62m during
Zambia’s Medicines Regulatory Authority (ZAMRA) and National Health Research Authority (NHRA) have signed a memorandum of understanding on the authorisation
Botswana’s medicines regulator has told importers, clearing agents and port of entry authorities that nine categories of medical devices and
South Africa’s Health Products Regulatory Authority (SAHPRA) has retained WHO Maturity Level 3 (ML3) for the regulation of vaccines as
Botswana’s medicines regulator has opened draft regulations under the Medicines and Related Substances Act 2025 for stakeholder comment, setting the
The Pharmacy and Poisons Board says the projects, ranging from a penicillin plant to vaccine and KEMRI facilities, support a target of producing half of essential health products locally.