The Department of Product Evaluation & Registration at BoMRA will conduct virtual stakeholder sessions to discuss the updates to medical devices including in vitro diagnostics (IVDs) regulatory processes. Discussions will include among others; medical devices regulatory strategy and roadmap, retentions, regulation enforcement, compliance, registration plan & requirements as well as any other relevant issues.
The stakeholder engagement sessions will be scheduled as follows:
SESSION 1: Wednesday 3rd September 2025 0900 – 1230hrs
SESSION 2: Thursday 4th September 2025 0900 – 1230hrs
Session 1 targets the following stakeholders dealing with medical devices including IVDs; Healthcare Facilities (Hospitals, Clinics, Medical Laboratories, etc.), Healthcare Professional Associations, Retailers, Pharmacies, Veterinary Outlets, Importers (logistics companies) and Import Control.
Session 2 targets the following stakeholders dealing with medical devices including IVDs; Manufacturers, Distributors, Wholesalers, Market Authorization Holders, Local Authorized Representatives and Importers.
Please use the links provided below to register your intention to attend the relevant stakeholder engagement session before the 1st September 2025 for planning purposes.
Session 1:
https://lnkd.in/dfYGUiHj
Session 2:
https://lnkd.in/d3xpptia
Kindly note that the content of the engagement sessions is targeted to the specified stakeholder groups. 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






