Dr. Marie Emad is a seasoned regulatory affairs specialist with over 12 years of experience in the medical device sector. In her current role, she leverages her expertise in medical device registration, variation assessment, and regulatory compliance to support the availability of safe and innovative healthcare technologies in Egypt.

Dr. Emad holds a Bachelor of Pharmaceutical Sciences and has dedicated her career to strengthening regulatory systems and promoting regulatory excellence. Prior to joining BD, she served as the Manager of the Evaluation Unit – Administration of Medical Devices Variation at the Egyptian Drug Authority (EDA). In this role, she was responsible for evaluating medical device variations, developing guidance documents, and contributing to the implementation of regulatory policies.

Her unique experience across both regulatory authority and industry environments allows her to combine deep technical knowledge with practical insights, making her a valuable contributor to advancing healthcare regulation in Egypt and beyond.