|
Mr. March joined Cytomedix in February, 2005, as its Director of Quality Assurance and Regulatory Affairs with more than 25 years of regulatory experience. Mr. March started his career as a Presidential Internship Award winner working at the Naval Aerospace Medical Research Laboratory in Pensacola, Florida. Following his work there and later with the Department of Defense, he joined the FDA in 1980, holding a number of positions in the Office of Device Evaluation and as a Compliance Officer for the Office of Compliance in the Center for Devices and Radiological Health. He was promoted to Assistant Director of the Division of Standards Enforcement, Office of Compliance where he directed the program for evaluating the conformance of medical devices to voluntary standards. Since 1994 and leaving FDA, Mr. March has been employed as a Senior Consultant to industry in the medical device regulatory area preparing applications for FDA approval of new medical devices and providing advice on FDA’s Quality System Regulation. He is an active member of the Regulatory Affairs Professional Society and the Association for the Advancement of Medical Instrumentation. Mr. March received a B.S. in Aerospace Engineering and M. S. degrees in Bioengineering and Management Science. | 