MindMed recruits regulatory expert ahead of Phase III trials

19 November 2024

New York-based Mind Medicine (Nasdaq: MNMD), a company developing MM120, a form of LSD (lysergide d-tartrate), for mental health conditions, has announced the appointment of Gregg Pratt (pictured, above), as chief regulatory and quality assurance officer.

Dr Pratt will serve as a member of the executive committee and oversee the company’s regulatory and quality functions, as well as its product registration strategies.

He brings more than three decades of experience in drug development, registration, and commercialization, with a career spanning multiple therapeutic areas including psychiatry, neurology, and cardiology. 

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