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 Medical Devices Module in the BoMRA Regulatory Information Management System (BRIMS). Your invaluable input is essential to ensure the success of this innovative regulatory platform.
About BRIMS-BoMRA Regulatory Information Management System (BRIMS) is a cutting-edge platform
designed to streamline regulatory processes and enhance collaboration among stakeholders. BRIMS
aims to provide a user-friendly, efficient, and transparent regulatory environment, benefiting all
stakeholders including businesses, regulatory agencies, and the public alike.
Why Participate
Early Access: Be among the first to experience the BRIMS platform and register into the system in
preparation for the upcoming registration of medical devices.
Provide Feedback: Your input will help BOMRA identify and address any issues or improvements
needed in the Medical Devices Registration and Exemption Module of BRIMS.
Shape the future: Contribute to the development and validation of a system that will impact regulatory
processes in a positive way.
The sessions will be scheduled as follows:
Virtual Session- Thursday 28 September 2023 0800hrs-1630hrs (Participants can join virtually
(Online Microsoft Teams), allowing for widespread participation.
Physical Session- Thursday 28 September 2023 0800hrs-1630hrs (A limited number of 30
participants can join in person for a more interactive experience)
Please use the link provided below to register your intention to attend the relevant stakeholder
engagement session by the 26th September 2023 for planning purposes. However, the session will
be limited to maximum of 1-2 representative(s) per company. The Representative should include an
Accountable Person. Detailed information regarding each stakeholder engagement session will be
communicated directly to the confirmed attendees.
Link: https://forms.gle/bak7D5GLBvrkKztP6
Participation in the BRIMS testing is voluntary and open to all stakeholders interested in improving
regulatory management processes. Your involvement is highly valued and will play a crucial role in the
success of BRIMS. We look forward to your participation and feedback to make BRIMS a powerful tool
for regulatory excellence.
Detailed information regarding each stakeholder engagement session will be communicated directly
to the confirmed attendees. For further questions on this notice or any other issues related to this
communication and/or session registration, kindly contact the Botswana Medicines Regulatory Authority at: medicaldevices.services@bomra.co.bw