Robert (Bob) joined Endeavour Vision in 2011 and brings exceptional insights into regulatory matters concerning the medical devices industry. Bob has been closely involved in several of the Endeavour II LP investments including Nfocus, Symetis and CeQur, and was part of the deal team for the EMG II fund’s investment in Rapid Micro Biosystems. Bob represents Endeavour Vision on the boards of CeQur, Nuvaira and Gynesonics.
Previously Bob was Worldwide Vice President of Regulatory Affairs for the Medical Devices and Diagnostics Group at Johnson & Johnson before retiring from the company in May 2008. Throughout his career, Bob has held both regulatory, R&D, and quality assurance positions with manufacturers of medical equipment, implants, and sterile disposables. He has managed sterilization laboratories, R&D IT functions, as well as Information Sciences, Regulatory Affairs, and Compliance Groups.
Bob has extensive experience in medical device regulatory submissions and played a key role in securing the approval of a number of novel products. These include absorbable implants, surgical staplers, orthopaedic implants, diagnostic devices, neurological devices, and combination products, including drug eluting stents. He also played a leadership role in establishing a global regulatory strategy for these products. He has been active with industry associations in the areas of product approval and FDA legislation. He has worked on every amendment to the medical device provisions of the US Food Drug and Cosmetic Act since 1980. He was also active in shaping the Medical Device Directive in the EU.
In 2002, Bob was awarded the Richard E. Greco Award, the highest honour bestowed by the Regulatory Affairs Professionals Society (RAPS). He was made Chairman of the society in 2006. Bob was also a member of the Food and Drug Law Institute’s Medical Devices committee and an industry representative to the FDA’s General and Plastic Surgery Advisory Panel. Bob has been honoured as an AdvaMed Achiever in recognition of his contributions on behalf of the medical device industry and has served on numerous AdvaMed Working Groups. He chaired the AdvaMed Technology and Regulatory Committee for 13 years in addition to playing key roles in over 20 other working groups. He chaired the User Fee Committee at AdvaMed for the first three user fee negotiations with FDA. Bob has also testified before the US Congress and Senate as well as EU authorities on various regulatory issues.
Bob graduated in Biology from Upsala College, US and then completed an MBA at Fairleigh, Dickinson University, US.
Bob holds a patent for an absorbable staple design and given his extensive knowledge of the sector, he is the author of several articles and book chapters on regulatory issues. He has also written several publications regarding health products.