Glenda Guest, BS, CCRA, RQAP-GCP, FACRP has over 20 years experience with regulated research involving pharmaceuticals, medical devices and biotech products. Through her experiences as a Quality Consultant and her years experience in a clinical CRO (NCRA) she's developed a unique perspective not only of the regulatory requirements for product development and market approval, but also insights from collaboration with multiple sponsor companies’ varying approaches in meeting those requirements.