​George, a U.S. citizen, brings extensive experience in medical device regulatory science, quality systems, and engineering. He has supervised and directed all aspects of compliance for more than 3,500 medical device products, including complex and high-risk technologies. His expertise spans FDA regulations, ISO 13485 quality systems, MDSAP, CE Marking, clinical evaluation, sterility assurance, combination products, and global market access.  Jenifer supports RegPro Medical in a business development role while continuing to own and operate specialty health services practices and provide practitioner training across Western Canada.

George & Jenifer, and their team, support international medical device manufacturers in the U.S. and Canadian markets, as well as North American companies seeking expansion into Europe and other global regions.