Chris A. Parr

Chris A. Parr, PMP has extensive work experience in regulatory affairs and quality assurance in the medical device industry. Chris A. is currently the Principal - Regulatory & Quality Practice at RQM+, where they serve as the technical lead for client projects in the medical device and in vitro diagnostic device sectors. Prior to this, they worked as the Head of Regulatory Affairs Europe - Medical Devices at Bausch + Lomb, leading a team of 15 RA Managers and Specialists across Europe. Chris A. also gained experience at MAETRICS, Merck Group, Cook Medical, Medtronic, and GSK, where they held various roles and responsibilities related to regulatory affairs and compliance. Overall, Chris possesses expertise in managing regulatory activities, submitting regulatory filings, ensuring compliance with industry standards, and building relationships with regulatory bodies.

Chris A. Parr, PMP completed a Bachelor of Science (Hons) in Chemistry at Heriot-Watt University from 1995 to 1999. Prior to that, Chris attended Monifieth High School from 1989 to 1995. In addition, Chris holds multiple certifications including a Project Management Professional (PMP) certification obtained in February 2024 and a Certified Associate in Project Management (CAPM) obtained in January 2023. They have also obtained various other certifications and completed training courses in project management, regulatory compliance, and quality management.