Robin has over 20 years of global real-world experience in the MedTech industry and regulatory pathways. Experience includes leadership roles in large, start-up and private equity entities. Passions include early regulatory and clinical strategy designs that align concepts/products, business strategy, and regulatory requirements so as to achieve safe and effective products that gain market authorizations.
Early collaboration and partnerships with incubators with novel technologies and cross functional teams has allowed me to provide predictable regulatory guidance in ever-changing regulatory landscapes. Technologies that include electromechanical-software and implants for orthopedics, spine, neuro, hepatic disease, ENT, and ophthalmology treatments have been areas of focus.
Robin holds a MSc from Grace College, Indiana in Regulatory and Clinical Affairs and an active Regulatory Affairs Certification (RACs) through the Regulatory Affairs Professional Society. Practical patient experience includes clinical and surgical ophthalmic technology in private and academic facilities.