Muna Kebede

Director of Regulatory Affairs and Clinical Studies, Akra Team, Germany

Muna Kebede is a Senior Consultant at AKRA TEAM GmbH, a company which was founded in 2021 to support various stakeholders in the healthcare system achieve their target. After graduating in Human Biology & Neurobiology, she perused an interest in pre- and post-market clinical research and entered the field of Medical Device Regulation in 2010. She has 10+ years’ experience in placing and maintaining Medical Devices on the market in Europe and globally. Before her current role in consultancy, Muna was Director of Regulatory Affairs & Clinical Studies and responsible for developing and implementing regulatory and clinical strategies for Class III Medical Devices. At AKRA Team GmbH, Muna helps manufacturers of all device classes navigate the requirements of the EU MDR, achieve, and maintain compliance and optimise related processes including those with their Notified Bodies and relevant Competent Authorities.