Providing an on-line discussion platform and document sharing platform for transmission of messages and information among users concerning oncology, cancer research, and general medical and health topics.

Providing online education, namely, providing online courses of instruction from a computer database or via the internet or extranet in the fields of clinical trials; providing online education, namely, providing online courses of instruction, namely, e-learning solutions relating to clinical trials in the field of medicine; developing, arranging, and conducting educational conferences in the field of clinical, medical, and biological research studies; educational services, namely, webinars, seminars, and conferences in the field of clinical, medical, and biological research studies; electronic publications in the nature of articles, blog posts, case studies, and e-learning modules in the field of clinical, medical, and biological research studies.

Providing information in the field of medical and scientific research on the internet; providing digital content, namely, e-learning solutions relating to clinical trials, on the internet; providing temporary use of on-line non-downloadable software for use by clinical, medical, and biological researchers, research sponsors and clinical research organizations in automating the submission, review and approval process of human subject clinical research projects and providing access to forms and templates to researchers, research sponsors and clinical research organizations for automating the submission, review and approval of human subject clinical research projects; providing temporary use of non-downloadable computer software for use in healthcare and research for the management and administration of research for the protection of research participants by automating the conduct of research studies and consent of research participants; organizing and administering a network of research sites that conduct gene therapy and vaccine research; providing institutional biosafety committee services, namely, review and oversight of clinical trials involving genetically engineered gene therapy and vaccine research; assessing the readiness of research sites to conduct gene therapy and vaccine research; coverage analysis services, namely, determining whether particular goods or services in clinical trials are covered by Medicare; consultation services in the nature of health inspection readiness and remediation and quality management in the field of clinical, medical, and biological research studies; consultation services in the field of drug and medical device development, clinical trial oversight and remediation, and pharmacovigilance strategies to ensure compliance and patient safety in the field of clinical trials involving human subjects; consultation services in the field of research compliance, administration, and operations in the field of clinical trials involving human subjects; consultation services in the field of product research and development and scientific research and development; consultation services in the field of informed consent protocols for clinical trial participants; consulting services in the field of medical and scientific research for clinical trials; non-downloadable software for use by clinical, medical, and biological research study sponsors, contract research organizations, research sites, and research site staff in the design, administration, and tracking of clinical, medical, and biological research studies; non-downloadable software for use by clinical, medical, and biological research study sponsors, contract research organizations, research sites, and research site staff in the storage, analysis, and transfer of data related to clinical, medical, and biological research studies; non-downloadable software for use in collecting and managing consents from participants in clinical, medical, and biological research studies; non-downloadable software for use by clinical, medical, and biological research study sponsors, contract research organizations, research sites, and research site staff in regulatory reporting, compliance tracking, safety monitoring, and evaluation of clinical, medical, and biological research studies; non-downloadable software enabling real-time communication for use by clinical, medical, and biological research study sponsors, contract research organizations, research sites, research site staff, and institutional review boards in clinical, medical, and biological research studies; non-downloadable software for use by clinical, medical, and biological research study sponsors, contract research organizations, research sites, and research site staff in managing stipends and travel reimbursements in clinical, medical, and biological research studies; non-downloadable software for use by pharmaceutical companies and clinical, medical, and biological research study sponsors, and contract research organizations in the design and administration of scientific and medical research projects and of clinical trials for pharmaceuticals, medical devices and medical procedures; non-downloadable software for use by pharmaceutical companies and clinical, medical, and biological research study sponsors, contract research organizations, research sites, and research site staff for data collection, data sharing, information exchange, and collaboration regarding scientific and medical research projects and regarding clinical trials for pharmaceuticals, medical devices and medical procedures; non-downloadable software in the nature of a support platform for use by clinical, medical, and biological research study sponsors, contract research organizations, research sites, research site staff, study teams and patients in the performance of a clinical trial; non-downloadable software in the nature of a clinical trial management system for use by academic medical centers and cancer centers; non-downloadable software in the nature of a clinical trial management system for use by clinical, medical, and biological research sites, site networks, hospitals, and health systems; non-downloadable teaching apparatus in the nature of an e-learning apparatus support platform for use by clinical, medical, and biological research site staff, study teams and patients relating to clinical trials; non-downloadable software in the nature of a patient identification system for use by clinical, medical, and biological researchers for patients enrolled in clinical trials; non-downloadable software in the nature of a patient scheduling and tracking system for use by clinical, medical, and biological research sites and patients enrolled in clinical trials; troubleshooting of computer software problems; providing temporary use of non-downloadable cloud-based software for transmitting clinical trial data.

Providing regulatory compliance consultation services in the nature of advice concerning due diligence, strategic development, and regulatory policy in the field of clinical trials involving human subjects; providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research; providing information relating to regulatory compliance for independent review of clinical trials involving human subjects.

Providing an on-line discussion platform and document sharing platform for transmission of messages and information among users concerning oncology, cancer research, and general medical and health topics.

Providing online education, namely, providing online courses of instruction from a computer database or via the internet or extranet in the fields of clinical trials; providing online education, namely, providing online courses of instruction, namely, e-learning solutions relating to clinical trials in the field of medicine; developing, arranging, and conducting educational conferences in the field of clinical, medical, and biological research studies; educational services, namely, webinars, seminars, and conferences in the field of clinical, medical, and biological research studies; electronic publications in the nature of articles, blog posts, case studies, and e-learning modules in the field of clinical, medical, and biological research studies.

Providing information in the field of medical and scientific research on the internet; providing digital content, namely, e-learning solutions relating to clinical trials, on the internet; providing temporary use of on-line non-downloadable software for use by clinical, medical, and biological researchers, research sponsors and clinical research organizations in automating the submission, review and approval process of human subject clinical research projects and providing access to forms and templates to researchers, research sponsors and clinical research organizations for automating the submission, review and approval of human subject clinical research projects; providing temporary use of non-downloadable computer software for use in healthcare and research for the management and administration of research for the protection of research participants by automating the conduct of research studies and consent of research participants; organizing and administering a network of research sites that conduct gene therapy and vaccine research; providing institutional biosafety committee services, namely, review and oversight of clinical trials involving genetically engineered gene therapy and vaccine research; assessing the readiness of research sites to conduct gene therapy and vaccine research; coverage analysis services, namely, determining whether particular goods or services in clinical trials are covered by Medicare; consultation services in the nature of health inspection readiness and remediation and quality management in the field of clinical, medical, and biological research studies; consultation services in the field of drug and medical device development, clinical trial oversight and remediation, and pharmacovigilance strategies to ensure compliance and patient safety in the field of clinical trials involving human subjects; consultation services in the field of research compliance, administration, and operations in the field of clinical trials involving human subjects; consultation services in the field of product research and development and scientific research and development; consultation services in the field of informed consent protocols for clinical trial participants; consulting services in the field of medical and scientific research for clinical trials; non-downloadable software for use by clinical, medical, and biological research study sponsors, contract research organizations, research sites, and research site staff in the design, administration, and tracking of clinical, medical, and biological research studies; non-downloadable software for use by clinical, medical, and biological research study sponsors, contract research organizations, research sites, and research site staff in the storage, analysis, and transfer of data related to clinical, medical, and biological research studies; non-downloadable software for use in collecting and managing consents from participants in clinical, medical, and biological research studies; non-downloadable software for use by clinical, medical, and biological research study sponsors, contract research organizations, research sites, and research site staff in regulatory reporting, compliance tracking, safety monitoring, and evaluation of clinical, medical, and biological research studies; non-downloadable software enabling real-time communication for use by clinical, medical, and biological research study sponsors, contract research organizations, research sites, research site staff, and institutional review boards in clinical, medical, and biological research studies; non-downloadable software for use by clinical, medical, and biological research study sponsors, contract research organizations, research sites, and research site staff in managing stipends and travel reimbursements in clinical, medical, and biological research studies; non-downloadable software for use by pharmaceutical companies and clinical, medical, and biological research study sponsors, and contract research organizations in the design and administration of scientific and medical research projects and of clinical trials for pharmaceuticals, medical devices and medical procedures; non-downloadable software for use by pharmaceutical companies and clinical, medical, and biological research study sponsors, contract research organizations, research sites, and research site staff for data collection, data sharing, information exchange, and collaboration regarding scientific and medical research projects and regarding clinical trials for pharmaceuticals, medical devices and medical procedures; non-downloadable software in the nature of a support platform for use by clinical, medical, and biological research study sponsors, contract research organizations, research sites, research site staff, study teams and patients in the performance of a clinical trial; non-downloadable software in the nature of a clinical trial management system for use by academic medical centers and cancer centers; non-downloadable software in the nature of a clinical trial management system for use by clinical, medical, and biological research sites, site networks, hospitals, and health systems; non-downloadable teaching apparatus in the nature of an e-learning apparatus support platform for use by clinical, medical, and biological research site staff, study teams and patients relating to clinical trials; non-downloadable software in the nature of a patient identification system for use by clinical, medical, and biological researchers for patients enrolled in clinical trials; non-downloadable software in the nature of a patient scheduling and tracking system for use by clinical, medical, and biological research sites and patients enrolled in clinical trials; troubleshooting of computer software problems; providing temporary use of non-downloadable cloud-based software for transmitting clinical trial data.

Providing regulatory compliance consultation services in the nature of advice concerning due diligence, strategic development, and regulatory policy in the field of clinical trials involving human subjects.