Christine Erickson

MS, M.Ed.

Principal Regulatory Consultant

Christine is a highly experienced regulatory affairs professional who began her career more than 18 years ago in a quality assurance role within the Drug-Eluting Stent analytical lab at Boston Scientific Corporation. Leveraging her advanced education including multiple master’s degrees and broad regulatory affairs and quality assurance expertise, she is a tremendous asset to MRC Global and the clients we serve.

Prior to joining MRC Global, Christine built her career as a Senior/Principal Regulatory Affairs Specialist at several industry leading medical device manufacturers including Wright Medical (part of Stryker Corporation), Torax Medical (part of Ethicon/J&J), Medtronic, and Boston Scientific Corporation.

Christine holds a Master in Regulatory Science (M.S.) from the University of St. Thomas (UST) in Saint Paul, Minnesota and a Master in Education (M.Ed, Learning Technologies) from the University of Minnesota in Minneapolis. She also holds a Bachelor of Arts (B.A.) majoring in biology from Hamline University in Saint Paul. In addition, Christine holds graduate certificate in medical device development (UST) and other specialized training and certifications in the areas of regulatory affairs, quality assurance, and advertising/promotion of medical devices.


  • 18+ years of medical device industry experience within quality assurance and regulatory affairs
  • Master in Regulatory Science
  • Master in Education (Learning Technologies)
  • Experience with FDA and international regulatory agency requirements and standards; medical device (PMA, HDE), devices and/or combination drug-device