|Medical Device Regulatory and Quality Compliance Consulting
Gary Riordan started Reg Pro 1, LLC in December 2010 and is the sole Sole Proprietor.
Mr. Riordan has extensive global regulatory and quality experience, including serving as a primary reviewer at the U.S. Food and Drug Administration (FDA). He was the V.P. of Quality and Regulatory Affairs at Sequenom and PrimeraDX. Mr. Riordan also worked at Ventana Medical Systems (a Member of the Roche Group), and at Roche Molecular Systems as Director, Regulatory Affairs. In these positions, he developed regulatory strategies and obtained many marketing authorizations. Mr. Riordan holds a B.A. in Molecular Biology, with a minor in Chemistry, from San Jose State University. He has co-authored articles published in peer-reviewed journals, and abstracts and posters for scientific conferences.