Ms. Christensen works with CardioMed Device Consultants as an affiliate consultant. She is a well-recognized regulatory and quality assurance consultant.
As an affiliate consultant, Anna Christensen brings over twelve years of medical device industry experience to CardioMed Device Consultants. Most recently, Ms. Christensen led a successful regulatory and quality assurance consulting business providing services for manufacturers of vascular stents, orthopedic devices, glucose monitors, and surgical instruments, among others. Her areas of expertise include the preparation of regulatory submissions, regulatory compliance, quality system development and implementation, and internal quality auditing.
Prior to consulting, she served as the head of regulatory affairs (RA) and quality assurance (QA) and as a principal RA/QA consultant for a testing lab and consulting firm, while supporting regulatory projects for its parent company. Additionally, she served several years in the regulatory affairs department of a multinational, cardiovascular device manufacturer.
Ms. Christensen is member of the Regulatory Affairs Professional Society (RAPS) and the American Society of Quality (ASQ).