Anna Christensen is an Affiliate Consultant with CardioMed Device Consultants and a well-recognized regulatory and quality assurance consultant with more than 12 years of medical device industry experience. Her expertise covers regulatory submissions, regulatory compliance, quality system development and implementation, and internal quality auditing.
Experience
Ms. Christensen most recently ran her own regulatory and quality assurance consulting business, supporting manufacturers of vascular stents, orthopedic devices, glucose monitors, and surgical instruments.
Earlier, she served as head of regulatory affairs and quality assurance and as a principal RA/QA consultant at a testing laboratory and consulting firm, where she also supported regulatory projects for its parent company. She began her career in the regulatory affairs department of a multinational cardiovascular device manufacturer.