Description: Class 35: Promoting public awareness of clinical trial results, namely, reporting and presentation of clinical trial results; Providing consulting services in the field of regulatory submission management to medical, biopharmaceutical and biotechnology companies to assist them with the submission of clinical trial results for applications for new pharmaceuticals and medical devices with governmental regulatory bodies; Regulatory submission management, namely, responding to inquiries regarding clinical trials from governmental regulatory bodies; Customer services, namely, responding to participant inquiries for others regarding clinical trials
Class 42: Consulting services for pharmaceutical, medical device, biotechnology, and medical research industries; consulting services in the field of expert review of proposed clinical trial design; software as a service (SaaS) featuring software for statistical analysis and simulation tools for clinical trial design, analysis, and optimization; providing an online non-downloadable computer software platform for running in vivo studies; providing an online non-downloadable computer software platform for running in silico studies; data modeling and statistical consulting services for the pharmaceutical, medical device, biotechnology, and medical research industries; design, development and implementation of software for in vivo simulations; design, development and implementation of software for in silico simulations
Class 45: Representation of clients in biomedical and pharmaceutical regulatory proceedings
