Retention of Products on the Botswana Medicines Registers
Reference is made to the above subject matter and the call for payment of annual retention fees letter MRA 1/9/2 vol I (126) and MRA
Virtual training For Local Representatives: The Common Technical Document (CTD)
The Botswana Medicines Regulatory Authority (BoMRA) will be conducting a virtual training on the basic principles of the Common Technical Document (CTD) for local representatives.
Physical Stakeholder Engagement Cosmetics and Medical Devices Including In Vitro Diagnostics
The Department of Product Evaluation & Registration at BoMRA will conduct in person stakeholderengagement sessions to discuss: Cosmetics – topics to be discussed include; cosmetics
Virtual Stakeholder Engagement – Cosmetics
The Department of Product Evaluation & Registration at BoMRA will conduct a virtual stakeholder sessions to discuss cosmetics listing findings, prohibited and restricted ingredients, legislative
Virtual Stakeholder Engagement – Medical Devices July 2022
The Botswana Medicines Regulatory Authority (BoMRA) through the department of Product Evaluation & Registration will conduct a virtual stakeholder engagement session to update the relevant