The Department of Product Evaluation & Registration (Medical Devices Unit) at BoMRA cordially invites all stakeholders to a consultative engagement meeting. Discussions will include among others:
- Legislative and regulatory requirements updates
- Medical devices registration roadmap
- Regulation enforcement and compliance updates
- Any other relevant regulatory matters
Target Audience: the engagement targets the following stakeholders dealing with medical devices including IVDs:
- Healthcare facilities (hospitals, clinics, medical laboratories, etc.), healthcare
professional associations, retailers, importers (logistics companies) and import control,
manufacturers, distributors, wholesalers, and local authorized representatives
Engagement details:
Session 1: Virtual, March 24th, 2026, at 08:30-12:30hrs
Please use the links provided below to register your intention to attend stakeholder engagement session before the March 13th, 2026, for planning purposes.
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






