Ysabel Fernando is an accomplished regulatory affairs professional with deep expertise in global regulatory pathways for pharmaceuticals, natural health products, medical devices, and environmental technologies. She has successfully supported and guided more than 60 product approvals worldwide.
Her regulatory experience spans key jurisdictions including the United States, Canada, and the European Union, with specialized knowledge of GRAS determinations, EFSA submissions, Health Canada approvals, and environmental and agricultural regulatory frameworks.
At Veos Pharma, Ms. Fernando leads regulatory strategy, compliance, and market entry planning, ensuring that the company’s innovative platforms meet the highest regulatory standards while enabling efficient global commercialization.
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