David Hammond

Director of MS in Biomedical Regulatory Affairs (BRAMS) Program, Teaching Associate Professor

Department of Pharmacy, Pharmacy Faculty, School Faculty

Education

  • MS in Biomedical Regulatory Affairs, University of Washington

Courses taught

  • PHRMRA 524: Introduction to Clinical Trials
  • PHRMRA 525: Implementation & Conduct of Clinical Trials
  • PHRMRA 526: Project Management & the Business of Clinical Trials
  • PHRMRA 527: International Regulatory Affairs
  • PHRMRA 548: Practicum
  • PHRMRA 554: Advanced Medical Products Regulation I

Biography

David Hammond is the Director of the BRAMS program, teaching associate professor in the Department of Pharmacy, and the lead for the Clinical Trials Certificate. He holds a Regulatory Affairs Certification in Medical Devices (RAC), the Certified IRB Professional (CIP), the Certified Clinical Research Professional (CCRP) and a number of other industry certifications. Hammond is the chair of an institutional review board and serves as a consultant to several biotechnology companies, providing guidance on regulatory strategy, clinical trial design and operations, and compliance with the FDA and other regulatory bodies around the world. He currently serves on the board of the Organization of Regulatory and Clinical Associates (ORCA) and was the inaugural recipient of the Martha Feldman Award for service and education to the regulatory community. Hammond is an alumnus of the UW BRAMS program.