Christopher Larson
Sr. Product Development Engineer
Chris Larson has over 15 years of experience as an engineer in the medical industry with the last 10 of those years being a Senior Product Development Engineer. His expertise ranges from Medical Device Product Development, QMS Creation and Remediation, DHF Creation and Remediation, and Data Analysis and Statistical Analysis.
As a Senior Product Development Engineer at Regulatory Compliance Associates® (RCA), Chris works with a wide variety of medical device development projects as a consultant on a team under the guidance of our Senior Consultants and Subject Matter Experts.
Chris has helped companies of various sizes develop class I, II, and III devices including orthopedic implants, combination devices, Software (in/as) a Medical Device, and sterile implants. This work has involved the development of user needs and design input requirements, creation of risk analysis and risk management documents, implementation of cybersecurity policies, and development of verification and validation testing plans.
Chris has his Master of Science in Biomedical Engineering from the New Jersey Institute of Technology in Newark, NJ and his Bachelor of Science in Biomedical Engineering from Rutgers University in New Brunswick, NJ.