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Matthew Hight, PhD

Assoc. Dir. Regulatory Affairs
Allucent

Matthew R. Hight, PhD, RAC is an Associate Director of Regulatory Affairs at Allucent, with an established record of successfully developing and managing regulatory strategies for investigational and marketing applications. He has more than 16 years of pharmaceutical development experience, including 10 years of regulatory affairs experience from multi-functional roles within small pharma and consulting firms. His knowledge of regulatory affairs spans a wide breadth of therapeutic indications and pharmaceutical product types (drugs, biologics, drug/device and biologic/device combination products), across early/late-stage development and post-market/commercial activities for various regulatory pathways.

Matthew is a skilled regulatory writer proficient in communicating complex ideas and has authored of various regulatory document types across the eCTD framework.

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