Dr. Marvin Turinaiwe
Marvin Turinaiwe is a pharmacist and Regulatory Officer at the National Drug Authority in Uganda, with three years of experience in the pharmaceutical sector. He specializes in the assessment and registration of drugs, medical devices, and healthcare products, ensuring compliance with regulatory standards. Marvin also has experience as an Analyst in the Quality Control Laboratory, […]
Dr. Maha Zahran
A pharmacist, holding a master’s degree in business administration with a focus on Health Economics from Arab Academy for Science, Technology and Maritime Transport with Regulatory affairs experience more than 9 years. She earned Regulatory Affairs Certificate in Medical devices from RAPS Online University since 2021 and ISO 13485:2016 Auditor/Lead Auditor from BSI since 2021.
Ms. Khatija Suleman
Khatija Suleman is a pharmacist with a postgraduate qualification in clinical pharmacology. She has 35 years of dynamic engagement in pharmaceuticals, medical devices, in-vitro diagnostics, clinical pharmacy and academia. Her experience and expertise in various sectors of the healthcare industry emanates from a wide range of roles and responsibilities in medical affairs, regulatory affairs, clinical […]
Ms. Khanyisile Nkuku
Ms Khanyisile Nkuku In her current role she contributes her expertise in the assessment and registration of medical devices & IVD’s in South Africa in an effort to promote medical device & IVD access on a global scale, with a particular focus on African countries. She holds a Bachelor of Pharmacy honours degree from the […]
Dr. Emil Ivan Mwikarago
Dr. Ivan Emil is a Microbiologist and a seasoned Public Health Laboratory Scientist with over a decade of experience as the Division Manager at Rwanda’s National Reference Laboratory. His management led to the laboratory attainment of ISO 15189. His extensive background encompasses regulatory affairs at national, regional, and international levels, with a strong emphasis on […]
Dr. Frank N. Laban
“Frank N Laban is a Pharmacist at the Zambia Medicines Regulatory Authority with 16 years of experience as a regulator in the area of medicines and medical devices regulation. Mr. Laban is responsible for supervising marketing authorization and related activities on Medical Devices and Human Medicines and is the country focal person for the WHO […]
Dr. Kone Dahafolo
Focal Point of the WHO-AIRP Collaborative Procedure for the Evaluation of In Vitro Diagnostic Medical Devices (IVDMs) for WHO Prequalification
Mr. Christopher Odero
Christopher serves as the Pan-Africa Regulatory Policy and Intelligence Partner at Roche Diagnostics, in Africa. Christopher also serves and leads various industry associations representing both local and multi-national companies. In Kenya, he is the Executive-Secretary of MEDAK (Medical Technology Industry Association of Kenya) as well as the Honorary Treasurer at KAPI (Kenya Association of Pharmaceutical […]
Mr. Dario Belluomini
He is the Manager International Affairs at MedTech Europe the European trade association for the medical technology industry including diagnostics, medical devices and digital health. In this position, Dario manages and coordinates projects and working groups addressing market access, trade policy initiatives and international regulatory matters in the medical technologies sector, with a primary focus […]
Dr. Dalia Safwat
Dalia Safwat is seasoned Quality assurance professional with Over 20 years in pharmaceutical industry. Dalia is dedicated to ensuring the highest standards of safety and quality in pharmaceutical practices. Core Qualifications: Strong Knowledge in Pharmaceutical industry. Strong Knowledge in Distributor quality management Strong Knowledge in Pharmacovigilance activities I am Currently serving as Quality assurance manager […]