Mr. Thabo B. Bokhutlo is a Medical Laboratory Scientist by profession. For the last 4 years, he has been involved in the Medical Devices including IVDs dossier assessments in the Department of Product Evaluation and Registration, at the Botswana Medicines Regulatory Authority (BoMRA) in Botswana. Prior to joining  BoMRA, he had been practicing as a Medical Laboratory Scientist under the Ministry of Health, Botswana for 4 years.  He holds a BSc in Medical Laboratory Sciences from the University of Botswana. He is passionate about the regulatory compliance of Medical Devices including In-vitro Diagnostics (IVDs). He has expertise in evaluating technical files and regulatory submissions to ensure compliance with local and international standards such as ISO 13485, and  ISO 14971. Skilled in assessing product safety, efficacy, and quality across various classes of medical devices including active devices and IVDs. He is committed to upholding regulatory requirements and contributing to patient safety through meticulous dossier assessment and regulatory compliance.