YES

Business consulting and management in the field of clinical trials, namely, clinical data and regulatory submission management on behalf of medical, biopharmaceutical and biotechnology companies to assist them with clinical research, clinical trials and applications for drug approval; regulatory submission management, namely, assisting others in preparing and filing applications for new drugs with governmental regulatory bodies; Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information for business purposes

Providing for the transmission, receipt, and exchange of, data and information on a computer network in the areas of medical research, pharmaceutical research and product regulatory approval

Consulting services in the fields of pharmaceutical research and development, laboratory testing, diagnostics, and pharmacovigilance