Botswana Health Emergency Preparedness, Response and Resilience Project Using the Multi-Phase Programmatic Approach (MPA)(P 510190)

The Republic of Botswana (the Recipient) is planning to implement the proposed Botswana Health Emergency Preparedness, Response and Resilience Project using the Multi-Phase Programmatic Approach
Botswana Health Emergency Preparedness, Response and Resilience Project Using the Multi-Phase Programmatic Approach (MPA)(P 510190)

Stakeholder Engagement Plan (SEP) This project is proposed under the Health Emergency Preparedness, Response and Resilience (HEPRR) Program using the Multiphase Programmatic Approach (MPA) and
CALL FOR PARTICIPATION IN BRIMS TESTING FOR MEDICAL DEVICES MODULE

Botswana Medicines Regulatory Authority (BoMRA) invites Medical Devices Stakeholders (Manufacturers, Distributors, Authorized Representatives etc.) to participate in the final testing and validation phase of the
STAKEHOLDER ENGAGEMENT-MEDICAL DEVICES INCLUDING IN VITRO DIAGNOSTICS

The Medical Devices Unit in the Department of Product Evaluation & Registration at BoMRAwill conduct stakeholder sessions to discuss the Medical Devices including In Vitro
Executive Leadership Announcements

The Board and Management at Botswana Medicines Regulatory Authority (BoMRA) wishes to announce the appointment of Shirley Amogelang Pine, as the Director, Human Resource & Organizational Development and Bathusi Kgosietsile as the Director, Product Evaluation and Registration.
CALL FOR VOLUNTARY PRIORITY BASED REGISTRATION OF MEDICAL DEVICES INCLUDING IVDS

As mandated by the Medicines and Related Substances Act of 2013, Botswana Medicines Regulatory Authority (BoMRA) is calling on applicants to register their medical devices
VIRTUAL STAKEHOLDER ENGAGEMENT-MEDICAL DEVICES INCLUDING IN VITRO DIAGNOSTICS

The Department of Product Evaluation & Registration at BoMRA will conduct virtualstakeholder sessions to discuss the medical devices including in vitro diagnostics(IVDs) registration timelines and
BoMRA Press Release MED Safety Week

The Botswana Medicines Regulatory Authority (BoMRA) is a new authority that is set up under the Medicines and Related Substances Act (MRSA) of 2013 and
BoMRA Medical Devices stakeholder engagement notice

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
Public Notice-COVID-19 Related medical Devices Exemptions Requirements

Botswana Medicines Regulatory Authority (BoMRA) would like to inform relevant stake holders that; that all Covid-19 related medical devices and IVDs should go through an






