Providing technical consulting services and information management services, namely, clinical data and regulatory submission management to medical, pharmaceutical and biotechnology companies to assist them with clinical research, clinical trials and applications for drug approval; providing the services of project management, namely, business project management in the field of clinical trials; providing the services of site management, namely, identifying, qualifying, and selecting sites for clinical trials, negotiating clinical trial site contracts and budgets, organizing and conducting business meetings of clinical trial investigators, assisting investigators with developing business strategies for recruiting clinical trial participants, submitting clinical trial protocols to institutional review boards and independent ethics committees, monitoring clinical trial investigators' activities for compliance with clinical protocols and regulations and for patient safety; providing the services of data management, namely, data compiling, analyzing and tracking in the field of clinical trials; providing the services of vendor management to medical, pharmaceutical, biopharmaceutical and biotechnology companies, namely, selecting and managing third-party providers of services that support clinical trials

Medical and scientific research, namely, conducting clinical trials, medical research, research in the field of biotechnology pharmaceutical research services, medical monitoring, pharmacovigilance in the nature of detection, assessment, and prevention of adverse effects of drugs and other drug-related problems, statistical analysis, medical writing, and drug logistics, all in the field of clinical research; maintenance of databases for others