Hammond Clinical Trial and FDA Medical Device Consulting
Providing FDA regulatory and clinical research consulting services at just the right level
About Hammond Clinical Trial Consulting, LLC
About Hammond CTC
Hammond Clinical Trial Consulting, LLC (also called Hammond CTC) was founded in 2008 with the goal of providing customized clinical research and regulatory consulting services to medical device and biotechnology companies.
Dave Hammond, the founder of Hammond CTC, is a veteran of medical technology development with more than 25 years of experience.
Dave began as a research coordinator at a site management organization and over the last, nearly, three decades has worked at a number of medical device, combination product, and biotechnology companies.
In addition to consulting, Dave is an Associate Teaching Professor at the University of Washington and academic director of their BRAMS program (MS in Biomedical Regulatory Affairs) in the School of Pharmacy.
Dave holds an MS in Regulatory Affairs, the RAC-Devices certification from the Regulatory Affairs Professional Society, the CCRP certification from the Society of Clinical Research Associates, and the ACRP-CP, ACRP-MDP, and ACRP-PM certifications from the Association of Clinical Research Professionals.
His areas of expertise include regulatory strategy, FDA submissions and negotiations, clinical trial design and management, training, and GCP compliance audits.