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Greg Cannedy joined Osteotech in May, 2006 as the Senior Director, Quality Assurance and Regulatory Affairs and was elected Vice President, Quality Assurance, Regulatory Affairs & Good Tissue Practices in May, 2007. Prior to joining Osteotech, Mr. Cannedy has over 20 years in the areas of regulatory affairs, quality systems, compliance and clinical affairs. Mr. Cannedy has consulted to both the IVD and medical device industries. Mr. Cannedy served as the Director, Regulatory Affairs for Medtronic Powered Surgical Solutions, and as a Senior Regulatory/Clinical Affairs Principle at DePuy-Acromed (a Johnson & Johnson Company). Mr. Cannedy was a sales representative for API and has held various clinical laboratory positions. Mr. Cannedy holds an EMBA from Cleveland State University and has a Bachelor's of Science in Medical Technology from Old Dominion University.
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