Douglas R. Dillon

Doug is responsible for managing Actuated’s ISO-certified quality management system (QMS). He ensures design and manufacturing compliance to ISO 13485, ISO 14971, 21 CFR 820, Medical Devices Directive 93/42/EEC, and the Medical Devices Single Audit Program (MDSAP). He is also responsible for submissions to regulatory bodies, including the U.S. Food and Drug Administration (FDA), Health Canada, and the European Union (EU). Doug earned his B.S. in Chemistry from Juniata College and his M.S. in Material Science and Engineering from Drexel University.