The Botswana Medicines Regulatory Authority (BoMRA) will be conducting virtual stakeholder engagements to
discuss the MRS ACT, Medical Devices Regulatory Framework, Medical Devices Exemptions and update on Listing
exercise. The roles played by Healthcare Facilities and Procurement Entities in ensuring that safe Medical Devices
and IVDs are imported into the country, services availed by BoMRA for facilities and more will be discussed. The
sessions will be scheduled as follows:
Notices
Lesotho Health Minister Leads Delegation on Benchmarking Visit to BoMRA
BOMRA Medical Devices including IVDs Regulatory Update.
Submission Of Veterinary Medicines Dossiers For The Reliance Based Expedited Registration
Public Notice – BoMRA CEO Calls For A Stronger Pharmaceutical Manufacturing Sector In Botswana
Public Notice – Happy Labour Day from BoMRA!
Public Notice -BoMRA Drives Dialogue On Traditional Medicines