Marcia Page joined Calypso Medical Technologies, Inc. in June 2002.

With over twenty-five years in the medical device industry in the quality, compliance and regulatory areas she oversees all aspects of quality systems including FDA, CMDCAS, MDD and ISO 13485 as well as regulatory product submissions.

Prior to joining Calypso Medical, Ms. Page was vice president of quality assurance and regulatory affairs for Plexus/SeaMED and corporate director of regulatory compliance and quality systems for Plexus Corporation, a contract design service provider for medical and complex high-tech products. Her responsibilities included ensuring compliance for multiple business divisions in various geographic locations. As a consultant with Noblitt and Rueland, a leading medical device consulting firm, she implemented compliant quality systems and identified and resolved problem areas for clients. 

Ms. Page attended Washington State University with a focus on business administration. She is a frequent instructor for the University of Washington Regulatory Affairs and Biomedical Certificate Program. Ms. Page is the past-president and Device Co-Chair for the Organization of Regulatory and Clinical Associates (ORCA).