Botswana Medicines Regulatory Authority (BoMRA) is embarking on a process to streamline the registration processes to facilitate quick access and availability of safe, quality and efficacious medical products (human medicines, veterinary medicines, complementary medicines and medical devices including IVDs) to Botswana market. BoMRA will be implementing a combined registration process (screening and evaluation) with a combined registration fee for registration of medical products effective from 1st October 2025
BoMRA is therefore calling for submission of all applications that were screened and had passed the screening process. Applicants should submit these applications for the registration procedure before or by the 30th September 2025. Applications that passed screening and not submitted for scientific evaluation by the given deadline (30th September2025), will be subjected to the revised submission requirements.
All screening applications that have received List of Questions (LoQs) from the Authority, and have gone beyond the deadline, shall automatically be closed, as pre-communicated in the LoQ letter.
The submissions are made online using the BRIMS self-service portal at: https://brims.bomra.co.bw/
For any system queries kindly contact helpdesk@bomra.co.bw
Please ignore this notice if you have already submitted all your products for scientific evaluation.






