Damaris DeGraft-Johnson, R. Ph.

Head, Regulatory Affairs

Over 18 years global regulatory experience in the pharmaceutical, device and biotechnology industries. Over 20 years hands-on experience in drug development including the areas of pre-formulation, formulation development, manufacturing transfer & scale-up, application of various analytical methodologies, contract manufacturing and life-cycle management. Currently, a global regulatory consultant to the pharmaceutical, device & biotechnology industries.