Mr. Thabo Bryan Bokhutlo
Mr. Thabo B. Bokhutlo is a Medical Laboratory Scientist by profession. For the last 3.5 years, he has been involved in the medical devices dossier assessments in the Department of Product Evaluation and Registration, at the Botswana Medicines Regulatory Authority (BoMRA) in Gaborone, Botswana. Prior to joining BoMRA, he had been practicing as a Medical […]
Dr. Shellan Omondi
Shellan Omondi is a regulatory officer at the Pharmacy and Poisons Board (PPB) in Kenya, where he is part of the Department of Product Evaluation and Registration in the Medical Devices and In Vitro Diagnostics (IVD) Unit. He oversees the evaluation and registration of medical devices and IVDs to ensure they meet safety, efficacy, and […]
Ms. Sarah Cohen
Ms Sarah Cohen, currently the Executive Officer at SALDA and an independent consultant, brings a wealth of expertise cultivated over a four-decade career in the medical and research industry. She obtained her Bachelors degree in Laboratory Management (Pretoria), Masters in Operations Management (Johannesburg) and MBA (Australia). Her contributions encompass training, coaching, and mentoring thus upskilling […]
Dr. Rafik Khazri
Dr. Rafik Khazri, pharmacist, charged of the Medical Devices Regulatory Affairs, leads the development of regulatory texts and the digital transformation initiatives at the National Agency of Medicines and Health Products in Tunisia. He oversees key projects, including the implementation of digital tools for regulatory processes. Dr. Khazri is a key player in advancing the […]
Dr. Rachel Juliet Mujawimana
Dr. Rachel J Mujawimana is a pharmacist with 14 years of experience in the pharmaceutical sector, covering community and regulatory pharmacy. She currently works as an Inspector of Drugs at the Uganda National Drug Authority, where she is responsible for ensuring the quality and safety of medicines and medical products in Uganda. Dr. Rachel is […]
Dr. Noha El Hariri
Dr. Noha El-Hariri is the General director of the general administration of medical devises registration -Egyptian drug authority (EDA) since 2020 and until now. She is also the supervisor of investment support & localization of medical devices, medical equipment & iVDs at EDA. In 2003 She had bachelor of clinical pharmacy with excellent grade with […]
Mrs. Simone Rudolph-Shortt
An Industrial Pharmacist of 30 years. Started her career at Adcock Ingram (pre – Sterling Winthrop) in production of Panado tablets and Syrup before moving to Smith & Nephew in 1992, which became BSNmedical (2001), National Bio-products (20004) as Pharmacist Plant Manager (ampoules / Vials ) followed by own Consulting business 2005. At Smith & […]
Mr. Rowland Sefakor
Mr. Rowland Sefakor, is the Head of the Medical Devices Department at the Food and Drugs Authority, Ghana. With over ten (10) years of experience in medical devices analysis, he has been instrumental in helping the medical devices laboratory achieve accreditation to ISO 17025 in eight (8) scopes, including sampling by attributes according to ISO […]
Mr. Monir El Azzouzi
Monir El Azzouzi is a Medical Device Expert specialized in Quality and Regulatory affairs. He has worked for multiple Medical Device company where he acquired 15 years of experience. Within his experience he had to develop Quality and Regulatory affairs departments, obtain CE marking for Medical Devices, register products all over the world, deal with […]
Dr. Miriam Boles
She holds a bachelor’s degree of pharmaceutical sciences from an established Egyptian university and a master’s degree in business administration from Arab Academy for Science, Technology & Maritime Transport, (AASTMT), where she specialized in supply chain. Miriam worked for two decades in various positions in medical device regulatory governmental sector. Prior to her current role, […]