Sara Horn, PhD

Clinical and Regulatory Affairs

Sara has more than 30 years of experience as a clinical and regulatory affairs expert and consultant, working with regulatory bodies in the US, Europe and Israel. Her experience includes leading clinical development programs in a variety of fields within the biotech and pharmaceuticals fields, developing regulatory strategies for various products (including drug, biologics and combination products), preparation and submission of regulatory files submissions, meetings with regulatory bodies as well as planning and conducting clinical studies. Under her supervisions a list of products have been approved in both US, EU and other countries worldwide. Sarah holds a PhD in Biochemistry and Immunology.