Mike is a medical device leader with proven track record over 20 years, of assisting companies with product development and commercialization —as well as over 15,000 hours of surgical and interventional procedural experience in animal, human cadaveric, and bench models. Mike has held various Management and Director roles within CROs and has been tapped as a Subject Matter Expert for US and OUS industry presentations and panels. Mike has co-authored multiple publications, abstracts, and posters. He founded Osiris Med Dev to collaboratively assist client core teams represented by R&D, regulatory, clinical, and quality experts in the development and implementation of efficient plans for successful global regulatory clearance, as well as sales force and end-user training for market adoption.

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