Vizma Carver has over 25 years successfully pioneering healthcare, life-science, and Health Information Technology (HIT) at FDA, DoD, VA and private industry. At FDA Centers for Devices and Radiological Health (CDRH) she was a Sr. Advisor in their Entrepreneur-In-Residence (EIR) program at their Innovation Center. There she co-led the workgroup on ‘Rebalancing the Pre- and Post- data requirements’. Additionally she facilitated the single protocol development between FDA CDRH Divisions, multiple medical device companies, Society for Vascular Surgery® and the registry developer. For the first-time in history, multiple companies are utilizing the identical protocol for their Post Approval Study, and shifting the data collection burden from Pre-Market to Post Approval Study with the use of a registry. Ms. Carver began her career successfully conducting stem cell R&D for a combination device through FDA approvals. She led the technical implementation of the first and only world-wide EHR system, and the development of one of the largest Health Information Exchange (HIE) systems between DoD and VA, setting several of the HIT standards currently used by EHRs.

Currently Ms. Carver is the Founder & CEO of Carver Global Health Group LLC, which has built a cloud based tool, ClearRoadmapTM to guide mHealth and medical device innovators from ‘Idea to MarketTM’.