The Department of Product Evaluation & Registration at BoMRA will conduct virtual
stakeholder sessions to discuss the medical devices including in vitro diagnostics
(IVDs) registration timelines and fees as well as updated exemptions guidelines.
The stakeholder engagement targets all relevant stakeholders inclusive of;
manufacturers, retailers, importers, distributors, local representatives, associations
The sessions will be scheduled as follows:
SESSION 1: Thursday 26th January 2023 0900 – 1200 hours
SESSION 2: Thursday 26th January 2023 1400 – 1700 hours
Please use the link provided below to register your intention to attend the relevant
stakeholder engagement session before the JANUARY 23 2023 for planning
purposes. Please, kindly note that the content of the two different engagement
sessions is the same. Additionally, detailed information regarding each stakeholder
engagement session will be communicated directly to the confirmed attendees.
If there are any further questions on this notice or any other issue related to this
communication, please kindly contact The Botswana Medicines Regulatory
Authority at: firstname.lastname@example.org