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Nanoscope Therapeutics Strengthens Clinical and Regulatory Expertise With Appointment of Samuel Barone, M D , as Chief Medical Officer

Part 1: FDA Workshop Highlights Global Regulatory View on Biosimilar Development

An FDA workshop featuring regulators from around the world provided the regulatory perspective on how each government determines whether a biosimilar is clinically equivalent to their reference product, highlighting the science behind their development guidelines.

Wilson Bryan, M D , Former Director of FDA CBER s Office of Tissues and Advanced Therapies, Joins Greenleaf

WASHINGTON (BUSINESS WIRE) Greenleaf Health, Inc. (Greenleaf), a leading Food and Drug Administration (FDA) regulatory consulting firm, today announces that Wilson Bryan, M.D., has joined as Executive Vice President, Drug and Biological Products. Wilson served as Director of the Office of Tissues and Advanced Ther.

Form 424B5 NeuBase Therapeutics,

Form 424B5 NeuBase Therapeutics,
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