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Nadia Ahankoob is a seasoned Senior Clinical and Regulatory Affairs Specialist with extensive experience in the medical devices industry. Nadia has a strong background in preparing regulatory submissions, ensuring compliance with global regulations, and overseeing post-market surveillance activities. Nadia has managed teams of medical writers and has a successful track record of authoring Clinical Evaluation Reports in accordance with regulatory requirements. With a Master’s degree in Bioscience Business and Medical Devices, Nadia brings a wealth of knowledge and expertise to their roles in various companies such as Zest Dental Solutions, Amgen, Abbott, and Edwards Lifesciences.