Month: July 2022

Analysing the availability of Medical Devices in 2022 in connection to the Medical Device Regulation (MDR) implementation

We are delighted to share with you the attached just-published MedTech Europe final survey report, “Analysing the availability of Medical Devices in 2022 in connection to the Medical Device Regulation (MDR) implementation”. You may also access it on the MedTech Europe website. Please feel free to share it with your members and contacts as you wish.

Virtual Stakeholder Engagement

The Botswana Medicines Regulatory Authority (BoMRA) through the department of Product Evaluation & Registration (DPER) will conduct a virtual stakeholder engagement session to update the relevant stakeholders on listing of medical devices, including In-Vitro Diagnostics (IVDs) devices.