Karissa Turtle Email Address

Microbiologist

A top CRO, and the world's only Medical Research Organization, we offer services for each phase of medical product development. Learn how we can help today.

Experienced Regulatory Affairs and Medical Writing Consultant with a demonstrated history of working in the medical device industry. Skilled in Medical Devices, U.S. Food and Drug Administration (FDA), EU Medical Device Directive (MDD), Medical Device Regulation (MDR), InVitro Diagnostic Regulation (IVDR), Design Control, Validation, Quality System and CAPA remediation. Masters of Science, Regulatory Affairs, focused in Regulatory Affairs and Services from UNIVERSITY OF ST. CLOUD MINNESOTA.