Chris Hendry is a veteran in the development and manufacture of protein biologics with an emphasis on selection and oversight of drug substance and drug product contract manufacturing organizations, development of commercial manufacturing processes, and quality risk management. He is also experienced in the transfer and validation of drug substance and drug product manufacturing processes; preparation of CMC sections of INDs, BLAs, and CTDs; project management of cross-functional development teams; and GMP facility and equipment design, validation, and development master planning. Mr. Hendry has a bachelor’s degree in biochemistry from the University of Maine.

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