Speakers

Laura Harner

Associate Director, Regulatory Affairs Biosimilars
Sandoz

Laura Harner is an Associate Director, Regulatory Affairs Biosimilars at Sandoz, where she is responsible for providing strategic and operational regulatory direction for biosimilar programs through development, registration, and approval. Prior to joining Sandoz, Laura spent 12 years working in different facets of regulatory at Novartis including Chemistry Manufacturing and Controls (CMC), Respiratory, Digital Health Innovation and Medical Devices. Previously, Laura developed and implemented global CMC strategy for drug and combination products through all stages of development at Schering-Plough and Merck.

Laura earned her Bachelor of Science in Biology from Fordham University and her Master of Science in Regulatory Affairs and Quality Assurance from Temple University.

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