معرفی
David Hammond is a Teaching Associate Professor at the University of Washington School of Pharmacy, where he serves as the Director of the MS in Biomedical Regulatory Affairs (BRAMS) Program and leads the Clinical Trials Certificate initiative. He holds the Regulatory Affairs Certification in Medical Devices (RAC), Certified IRB Professional (CIP), and Certified Clinical Research Professional (CCRP), alongside other industry certifications.
Education
- MS in Biomedical Regulatory Affairs, University of Washington
Hammond's expertise spans biotechnology, regulatory affairs, and clinical trial design. He chairs an institutional review board and consults for biotechnology companies on global regulatory compliance, including FDA and international standards. His work emphasizes the intersection of medical product regulation, project management, and clinical operations.
He is actively involved in professional service as a board member of the Organization of Regulatory and Clinical Associates (ORCA) and was the inaugural recipient of the Martha Feldman Award, recognizing his contributions to regulatory education and community service.
Hammond teaches courses in clinical trials, regulatory affairs, and project management, including PHRMRA 524 through PHRMRA 554, and is an alumnus of the UW BRAMS program.
