Lars Guntveit is from the 1st of January 2015 employed as Regulatory Manager Medical Device in LINK Medical Research. Lars has previous experience from Medistim ASA as VP Regulatory Affairs and from Alertis Medical ASA as VP Technology development. He has broad experience from regulatory requirements and documentation required for obtaining CE-mark in Europe and FDA 510(k) clearance in US for medical devices.
Lars holds a University degree from University of Salford, Manchester, England within Electronic Computer Systems. In addition to his regulatory expertise Lars also has many years of experience of product development and project management from other industries.
We are very happy to welcome Lars Guntveit to our Medical Device team.