Classe 35
Data management, namely, abstraction and collection of medical data from clinical tests for business purposesmarket research and business marketing consulting services in the pharmaceutical, biotechnology, medical device, and diagnostics industries
Classe 42
Programming of software for managing and collecting patient-generated health data for scientific research purposescloud computing featuring software that allows users to collect, review, analyze and report on clinical researchtechnical support services, namely, installation and remote administration of software, and troubleshooting of software problems and hosted software applications, all for use in connection with medical research and product regulatory approval, environmental health, health care, and in relation to the design, research, development, and testing of new medical products and devicescloud computing featuring software for providing telehealth, telemedicine, remote care and virtual health care services to patientscloud computing featuring software that allows users to collect, track, retrieve, validate, summarize, statistically analyze and present data used in the areas of medical research and product regulatory approval, environmental health, health care, and in relation to the design, research, development, and testing of new medical products and devicescloud computing featuring software to aggregate, integrate, transfer and manage data generated from home health and remote monitoring devices and applications and health-related smart-phone applicationscloud computing featuring software that provides integrated workflows, analytics, visualizations, and reporting features to deliver, process, analyze, elevate, and display patient-generated health datacloud computing featuring software that integrates remotely collected health data into databases, systems, platforms, applications, and software that inform clinical research, remote monitoring, and care managementhosting of web-based portal for study sponsors and contract research organizations (CROS) to build programs, enroll members, automate actions, and visualize/analyze data in connection with clinical studiestechnical consulting services, namely, evaluating the safety of pharmaceutical, medical, cosmetic and consumer devices and products in clinical development or in commercial productionconsulting services for others in the field of design, planning, and implementation project management of clinical trialsanalysis of statistical data relating to clinical trials for pharmaceuticals, biotechnology, medical devices and diagnostics for scientific research
Classe 45
Development of regulatory compliance strategies in the field of medical research, namely, regulatory compliance in drug, biologic, cosmetic and medical device development