Houda Khamis is a Senior Regulatory Affairs Specialist with over 10 years of experience in medical devices, pharmaceuticals, and Advanced Therapy Medicinal Products (ATMPs). They currently serve as a Senior Regulatory Affairs Specialist for Belgium and Luxembourg at Abbott, following their role as Regulatory Affairs Manager at Novadip Biosciences. Khamis earned a PhD in Molecular Biology from the Université de Namur, where they conducted research on traits and genes related to agriculture. They have a proven track record in EU and FDA regulatory submissions, clinical trial management, and providing strategic regulatory intelligence.
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