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Press Releases
BoMRA Press Release Stakeholder Engagement November
BoMRA will conduct stakeholder sessions to discuss the regulatory requirements for medical devices.
BoMRA Press Release DPER Stakeholder engagements (October)
The Department of Product Evaluation & Registration at BoMRA will conduct stakeholder sessions to discuss the registration requirements for medical devices, veterinary medicines, human medicines
Expression of interest (Calibration of Infrared Thermometers)
The Botswana Medicines Regulatory Authority (BoMRA) is responsible for regulating the supply chain of human and veterinary medicines, medical devices and cosmetics to ensure their
Suspension Of Registration of GrandPa Products
The public, healthcare practitioners, importers and distributors are informed that registrations of Grand-Pa Headache products (Powder and tablets) have been suspended from the Botswana market
Call for Registration of medical devices distributors
Botswana Medicines Regulatory Authority (BoMRA) is calling on all entities trading in medical devices to register with the Authority.
Important Public Warning
Botswana Medicines Regulatory Authority (BoMRA) reminds consumers to be cautious of stores and websites selling products that claim to prevent, mitigate, treat, diagnose or cure