VEO

business consulting and management in the field of clinical trials, namely, clinical data and regulatory submission management on behalf of medical device and pharmaceutical companies to assist them with clinical research, clinical trials, and applications for the approval by governmental regulatory bodies of medical devices, pharmaceuticals, and combination products

regulatory submission management, namely, assisting others in preparing and filing applications with governmental regulatory bodies for new medical devices and pharmaceuticals or combinations thereof, including but not limited to new medical devices and pharmaceuticals for the eye