Botswana Medicines Regulatory Authority (BoMRA) invites Medical Devices Stakeholders (Manufacturers, Distributors, Authorized Representatives etc.) to participate in the final testing and validation phase of the
The Medical Devices Unit in the Department of Product Evaluation & Registration at BoMRAwill conduct stakeholder sessions to discuss the Medical Devices including In Vitro
The Board and Management at Botswana Medicines Regulatory Authority (BoMRA) wishes to announce the appointment of Shirley Amogelang Pine, as the Director, Human Resource & Organizational Development and Bathusi Kgosietsile as the Director, Product Evaluation and Registration.
As mandated by the Medicines and Related Substances Act of 2013, Botswana Medicines Regulatory Authority (BoMRA) is calling on applicants to register their medical devices
The Department of Product Evaluation & Registration at BoMRA will conduct virtualstakeholder sessions to discuss the medical devices including in vitro diagnostics(IVDs) registration timelines and