Peggy Carter BA, PhD

Peggy have over ten years of In Vitro Diagnostic industry experience with a broad knowledge of Molecular Biology and Biochemistry in the IVD regulated environment. The focus of the last six years has been on in vitro companion diagnostic devices. She have a proven track record of premarket submissions including 510(k)s for five products within three years. She have successfully submitted both original PMA and PMA supplements (180 and 30 day). She also have experience with pre-IDE and IDE submissions and other FDA communications and face to face meetings . She enjoy working in a results oriented environment facilitating the design of innovative and quality products that improve the lives of patients.