
The Botswana Medicines Regulatory Authority (BoMRA) is the statutory body regulating medicines, medical devices, cosmetics and related health products in Botswana. It oversees registration, licensing and authorisation of human and veterinary medicines, complementary medicines, medical devices and cosmetics before market entry. BoMRA also conducts inspections, enforces compliance and monitors clinical trials to ensure products meet safety and quality standards.
Its website offers regulatory forms, guidelines, legislation, fee schedules and product registers for manufacturers, importers, healthcare professionals and the public. The site supports pharmacovigilance, including reporting of adverse drug reactions, side effects and safety alerts or recalls. It also provides tender notices, career opportunities, press releases and a complaints system for service-related concerns.
Keep Browsing




