Travis Arola has 20 years of industry experience in the development and commercialization of new medical technologies.  Travis has validated software and implemented processes for quality management system and document control in a biotech company.  He has submitted 31 510(k)s, 2 IDEs, multiple pre-IDEs and pre-Subs, 4 Canadian Class IV approvals, 2 Australian Class III approvals, and multiple Class I, IIa, IIb and III CE Mark devices.  He developed and manages the project and facility risk management program for a local biotech company.  Travis has a BS in Mechanical Engineering from Ohio University, an MS in Materials Science and Engineering from the University of Florida, AATB CTBS accreditation, and RAPS Regulatory Affairs Certification.