Medical Device Regulatory Advisors, Inc. (MDRA) was founded in 1998 by Mr. Robert Clark to fill what he saw as a particular need for technically competent regulatory and quality system expertise.  His professional background encompasses over 30 years of product development, manufacturing, quality assurance, and regulatory affairs, working both domestically and internationally with a broad group of FDA regulated biomedical companies.

He has authored and presented educational articles and participated in regional and national biomedical industry seminars.  Mr. Clark is Regulatory Affairs Certified (RAC), and holds degrees in Physics and Electrical Engineering.