ADVARRA, INC.

Software as a service (SaaS) services featuring software using artificial intelligence to improve the design and operational efficiency of clinical trials by means of generating actionable insights, predictions, and workflow automation; Software as a service (SaaS) services featuring software using artificial intelligence to extract structured and unstructured data from clinical trial protocols to create, de-identify, encrypt, standardize and tokenize machine readable data; Software as a service (SaaS) featuring software for use in providing a data clean room enabling researchers to securely access and analyze digitized clinical trial protocol data; Software as a service (SaaS) services featuring software using artificial intelligence to optimize clinical research protocols and study feasibility by benchmarking a given protocol against the operational outcomes of similar past protocols; Software as a service (SaaS) services featuring software using artificial intelligence that enables researchers to engage in predictive planning to model the budget, timeline, enrollment, site performance, and investigator trends in clinical research; Software as a service (SaaS) services featuring software using artificial intelligence to automate Institutional Review Board (IRB) workflow for submission validation, conversational guidance and digital protocol delivery; Software as a service (SaaS) services featuring software using artificial intelligence to enable research study startup workflows that digitize artifacts, research site communications, predictive planning, and regulatory tracking for accelerated initiation of research sites; Software as a service (SaaS) services featuring software using artificial intelligence and integrated workflow automation to plan, track, and manage clinical trial operations at research sites effectively with real-time visibility to identify opportunities for further efficiency; Providing temporary use of online non-downloadable chatbot software using artificial intelligence to respond to natural language queries from researchers with charts, summaries, and follow-up prompts; Software as a service (SaaS) services featuring software using artificial intelligence to create research data visualizations that automatically generate dashboards, graphing, and charting for evidence-backed insights; Software as a service (SaaS) services featuring software using artificial intelligence to forecast and recommend actions that enable researchers to improve the design, planning, and execution of clinical trials

Software as a service (SaaS) services featuring software using artificial intelligence to improve the design and operational efficiency of clinical trials by means of generating actionable insights, predictions, and workflow automation; Software as a service (SaaS) services featuring software using artificial intelligence to extract structured and unstructured data from clinical trial protocols to create, de-identify, encrypt, standardize and tokenize machine readable data; Software as a service (SaaS) featuring software for use in providing a data clean room enabling researchers to securely access and analyze digitized clinical trial protocol data; Software as a service (SaaS) services featuring software using artificial intelligence to optimize clinical research protocols and study feasibility by benchmarking a given protocol against the operational outcomes of similar past protocols; Software as a service (SaaS) services featuring software using artificial intelligence that enables researchers to engage in predictive planning to model the budget, timeline, enrollment, site performance, and investigator trends in clinical research; Software as a service (SaaS) services featuring software using artificial intelligence to automate Institutional Review Board (IRB) workflow for submission validation, conversational guidance and digital protocol delivery; Software as a service (SaaS) services featuring software using artificial intelligence to enable research study startup workflows that digitize artifacts, research site communications, predictive planning, and regulatory tracking for accelerated initiation of research sites; Software as a service (SaaS) services featuring software using artificial intelligence and integrated workflow automation to plan, track, and manage clinical trial operations at research sites effectively with real-time visibility to identify opportunities for further efficiency; Providing temporary use of online non-downloadable chatbot software using artificial intelligence to respond to natural language queries from researchers with charts, summaries, and follow-up prompts; Software as a service (SaaS) services featuring software using artificial intelligence to create research data visualizations that automatically generate dashboards, graphing, and charting for evidence-backed insights; Software as a service (SaaS) services featuring software using artificial intelligence to forecast and recommend actions that enable researchers to improve the design, planning, and execution of clinical trials

Software as a service (SaaS) services featuring software using artificial intelligence to improve the design and operational efficiency of clinical trials by means of generating actionable insights, predictions, and workflow automation; Software as a service (SaaS) services featuring software using artificial intelligence to extract structured and unstructured data from clinical trial protocols to create, de-identify, encrypt, standardize and tokenize machine readable data; Software as a service (SaaS) featuring software for use in providing a data clean room enabling researchers to securely access and analyze digitized clinical trial protocol data; Software as a service (SaaS) services featuring software using artificial intelligence to optimize clinical research protocols and study feasibility by benchmarking a given protocol against the operational outcomes of similar past protocols; Software as a service (SaaS) services featuring software using artificial intelligence that enables researchers to engage in predictive planning to model the budget, timeline, enrollment, site performance, and investigator trends in clinical research; Software as a service (SaaS) services featuring software using artificial intelligence to automate Institutional Review Board (IRB) workflow for submission validation, conversational guidance and digital protocol delivery; Software as a service (SaaS) services featuring software using artificial intelligence to enable research study startup workflows that digitize artifacts, research site communications, predictive planning, and regulatory tracking for accelerated initiation of research sites; Software as a service (SaaS) services featuring software using artificial intelligence and integrated workflow automation to plan, track, and manage clinical trial operations at research sites effectively with real-time visibility to identify opportunities for further efficiency; Providing temporary use of online non-downloadable chatbot software using artificial intelligence to respond to natural language queries from researchers with charts, summaries, and follow-up prompts; Software as a service (SaaS) services featuring software using artificial intelligence to create research data visualizations that automatically generate dashboards, graphing, and charting for evidence-backed insights; Software as a service (SaaS) services featuring software using artificial intelligence to forecast and recommend actions that enable researchers to improve the design, planning, and execution of clinical trials

Education services, namely, providing non-downloadable webinars in the field of oncology research; Education services, namely, providing panel discussions in the field of oncology research; Arranging and conducting of conferences in the field of oncology research; Providing in-person educational forums in the field of oncology research; Arranging and conducting of seminars in the field of oncology research; Providing on-line non-downloadable articles in the field of oncology research; Online publication of blogs; Downloadable webinars in the field of oncology research; Downloadable written articles in the field of oncology research; Providing online educational forums in the field of oncology research; Printed articles in the field of oncology research

Downloadable electronic publications in the nature of articles, case studies, and e-learning modules in the field of clinical, medical, and biological research studies | Business consulting; business administrative assistance, namely, business support services for the preparation and filing of institutional biosafety committee and institutional review board forms for use in the field of human subject research; business management consultation services concerning organization transformation in the field of clinical trials involving human subjects; professional staffing services in the field of medical and scientific research; organizing and administering a network of research sites, namely, business consultation and management in the field of clinical trials, specifically, providing governmental registration assistance in the nature of regulatory submission management on behalf of research sites that conduct gene therapy and vaccine research to assist them with clinical research and clinical trials; providing institutional biosafety committee services, namely, providing independent review and oversight of clinical trials involving genetically engineered gene therapy and vaccine research for business purposes | Financial advisory services, namely, budget negotiation and budget set-up services in the field of clinical trials involving human subjects; insurance coverage consultancy services, namely, determining whether particular goods and services in clinical trials are covered by Medicare | Providing an on-line discussion platform and document sharing platform in the nature of an on-line forum for transmission of messages and information among computer 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; developing, arranging, and conducting educational conferences in the field of clinical, medical, and biological research studies; educational services, namely, providing online, non-downloadable webinars, seminars, and conferences in the field of clinical, medical, and biological research studies; non-downloadable 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; developing, arranging and conducting business conferences 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 in the nature of software as a service (SAAS) services featuring software for database management and information management 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 for use 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; providing institutional biosafety committee services, namely, review and oversight of clinical trials involving genetically engineered gene therapy and vaccine research, specifically, evaluating research sites involved in gene therapy and vaccine research clinical trials to determine whether the organizations conform to an established accreditation standard; assessing the readiness of research sites to conduct gene therapy and vaccine research, namely, testing, analysis, and evaluation of gene therapy and vaccine research service providers to determine conformity with established accreditation standards; consultation services in the nature of quality management, namely, quality evaluation and analysis, quality assurance, and quality control in the field of clinical, medical, and biological research studies; consultation services in the field of drug and medical device development; consultation services in the field of conducting clinical trials for others; consultation services in the field of scientific research compliance, namely, analysis and evaluation of scientific research of others in the field of clinical trials involving human subjects to assure compliance with industry standards; consultation services in the field of scientific research 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; consulting services in the field of medical and scientific research for clinical trials; providing online non-downloadable software for use by clinical, medical, and biological research study sponsors, contract research organizations, research sites, and research site staff for use in the design, administration, and tracking of clinical, medical, and biological research studies; providing online 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; providing online non-downloadable software for use in collecting and managing consents from participants in clinical, medical, and biological research studies; providing online 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; providing online 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; providing online 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; providing online 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; providing online 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; providing online 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 for use in information management in the performance of a clinical trial; providing online non-downloadable software in the nature of a clinical trial management system for data processing and information management for use by academic medical centers and cancer centers; providing online non-downloadable software in the nature of a clinical trial management system for data processing and information management for use by clinical, medical, and biological research sites, site networks, hospitals, and health systems; providing online non-downloadable teaching software system in the nature of an e-learning apparatus support platform for content delivery, patient recruitment management, and learning process management and reporting for use by clinical, medical, and biological research site staff, study teams and patients relating to clinical trials; providing online non-downloadable software for patient identification for use by clinical, medical, and biological researchers for patients enrolled in clinical trials; providing online non-downloadable software for patient scheduling and tracking 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; business technology software consultation services regarding the implementation of computer software provided online for use in healthcare and research that is for the management and administration of research, the protection of research participants, and the automation and facilitation of the conduct of research studies and electronic consent of research participants; providing online education, namely, software as a service (SAAS) services featuring e-learning software for providing online courses of instruction relating to clinical trials in the field of medicine | 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 institutional biosafety committee services, namely, independent review and oversight of clinical trials involving genetically engineered gene therapy and vaccine research, specifically, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research; assessing the readiness of research sites to conduct gene therapy and vaccine research, namely, reviewing standards and practices to assure compliance with laws and regulations in the field of clinical trials involving human subjects; regulatory compliance consultation services in the nature of health inspection readiness and remediation in the field of clinical, medical, and biological research studies; consultation services in the field of pharmacovigilance strategies to ensure regulatory compliance and patient safety in the field of clinical trials involving human subjects; regulatory compliance consultation services in the field of informed consent protocols for clinical trial participants; consultation services in the field of research compliance, namely, regulatory compliance consultation services in the field of clinical trials involving human subjects

Business consulting; business administrative assistance, namely, business support services for the preparation and filing of institutional biosafety committee and institutional review board forms for use in the field of human subject research; business management consultation services concerning organization transformation in the field of clinical trials involving human subjects; professional staffing services in the field of medical and scientific research; organizing and administering a network of research sites, namely, business consultation and management in the field of clinical trials, specifically, providing governmental registration assistance in the nature of regulatory submission management on behalf of research sites that conduct gene therapy and vaccine research to assist them with clinical research and clinical trials; providing institutional biosafety committee services, namely, providing independent review and oversight of clinical trials involving genetically engineered gene therapy and vaccine research for business purposes | Financial advisory services, namely, budget negotiation and budget set-up services in the field of clinical trials involving human subjects; insurance coverage consultancy services, namely, determining whether particular goods and services in clinical trials are covered by Medicare | Providing an on-line discussion platform and document sharing platform in the nature of an on-line forum for transmission of messages and information among computer 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; developing, arranging, and conducting educational conferences in the field of clinical, medical, and biological research studies; educational services, namely, providing online, non-downloadable webinars, seminars, and conferences in the field of clinical, medical, and biological research studies; non-downloadable 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; developing, arranging and conducting business conferences 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 in the nature of software as a service (SAAS) services featuring software for database management and information management 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 for use 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; providing institutional biosafety committee services, namely, review and oversight of clinical trials involving genetically engineered gene therapy and vaccine research, specifically, evaluating research sites involved in gene therapy and vaccine research clinical trials to determine whether the organizations conform to an established accreditation standard; assessing the readiness of research sites to conduct gene therapy and vaccine research, namely, testing, analysis, and evaluation of gene therapy and vaccine research service providers to determine conformity with established accreditation standards; consultation services in the nature of quality management, namely, quality evaluation and analysis, quality assurance, and quality control in the field of clinical, medical, and biological research studies; consultation services in the field of drug and medical device development; consultation services in the field of conducting clinical trials for others; consultation services in the field of scientific research compliance, namely, analysis and evaluation of scientific research of others in the field of clinical trials involving human subjects to assure compliance with industry standards; consultation services in the field of scientific research 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; consulting services in the field of medical and scientific research for clinical trials; providing online non-downloadable software for use by clinical, medical, and biological research study sponsors, contract research organizations, research sites, and research site staff for use in the design, administration, and tracking of clinical, medical, and biological research studies; providing online 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; providing online non-downloadable software for use in collecting and managing consents from participants in clinical, medical, and biological research studies; providing online 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; providing online 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; providing online 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; providing online 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; providing online 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; providing online 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 for use in information management in the performance of a clinical trial; providing online non-downloadable software in the nature of a clinical trial management system for data processing and information management for use by academic medical centers and cancer centers; providing online non-downloadable software in the nature of a clinical trial management system for data processing and information management for use by clinical, medical, and biological research sites, site networks, hospitals, and health systems; providing online non-downloadable teaching software system in the nature of an e-learning apparatus support platform for content delivery, patient recruitment management, and learning process management and reporting for use by clinical, medical, and biological research site staff, study teams and patients relating to clinical trials; providing online non-downloadable software for patient identification for use by clinical, medical, and biological researchers for patients enrolled in clinical trials; providing online non-downloadable software for patient scheduling and tracking 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; business technology software consultation services regarding the implementation of computer software provided online for use in healthcare and research that is for the management and administration of research, the protection of research participants, and the automation and facilitation of the conduct of research studies and electronic consent of research participants; providing online education, namely, software as a service (SAAS) services featuring e-learning software for providing online courses of instruction relating to clinical trials in the field of medicine | 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 institutional biosafety committee services, namely, independent review and oversight of clinical trials involving genetically engineered gene therapy and vaccine research, specifically, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research; assessing the readiness of research sites to conduct gene therapy and vaccine research, namely, reviewing standards and practices to assure compliance with laws and regulations in the field of clinical trials involving human subjects; regulatory compliance consultation services in the nature of health inspection readiness and remediation in the field of clinical, medical, and biological research studies; consultation services in the field of pharmacovigilance strategies to ensure regulatory compliance and patient safety in the field of clinical trials involving human subjects; regulatory compliance consultation services in the field of informed consent protocols for clinical trial participants; consultation services in the field of research compliance, namely, regulatory compliance consultation services in the field of clinical trials involving human subjects

Business consulting; business administrative assistance, namely, business support services for the preparation and filing of institutional biosafety committee and institutional review board forms for use in the field of human subject research; business management consultation services concerning organization transformation in the field of clinical trials involving human subjects; professional staffing services in the field of medical and scientific research; organizing and administering a network of research sites, namely, business consultation and management in the field of clinical trials, specifically, providing governmental registration assistance in the nature of regulatory submission management on behalf of research sites that conduct gene therapy and vaccine research to assist them with clinical research and clinical trials; providing institutional biosafety committee services, namely, providing independent review and oversight of clinical trials involving genetically engineered gene therapy and vaccine research for business purposes | Financial advisory services, namely, budget negotiation and budget set-up services in the field of clinical trials involving human subjects; insurance coverage consultancy services, namely, determining whether particular goods and services in clinical trials are covered by Medicare | 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; developing, arranging, and conducting educational conferences in the field of clinical, medical, and biological research studies; educational services, namely, providing online, non-downloadable webinars, seminars, and conferences in the field of clinical, medical, and biological research studies; non-downloadable 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; developing, arranging and conducting business conferences 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 in the nature of software as a service (SAAS) services featuring software for database management and information management 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 for use 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; providing institutional biosafety committee services, namely, review and oversight of clinical trials involving genetically engineered gene therapy and vaccine research, specifically, evaluating research sites involved in gene therapy and vaccine research clinical trials to determine whether the organizations conform to an established accreditation standard; assessing the readiness of research sites to conduct gene therapy and vaccine research, namely, testing, analysis, and evaluation of gene therapy and vaccine research service providers to determine conformity with established accreditation standards; consultation services in the nature of quality management, namely, quality evaluation and analysis, quality assurance, and quality control in the field of clinical, medical, and biological research studies; consultation services in the field of drug and medical device development; consultation services in the field of conducting clinical trials for others; consultation services in the field of scientific research compliance, namely, analysis and evaluation of scientific research of others in the field of clinical trials involving human subjects to assure compliance with industry standards; consultation services in the field of scientific research 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; consulting services in the field of medical and scientific research for clinical trials; providing online non-downloadable software for use by clinical, medical, and biological research study sponsors, contract research organizations, research sites, and research site staff for use in the design, administration, and tracking of clinical, medical, and biological research studies; providing online 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; providing online non-downloadable software for use in collecting and managing consents from participants in clinical, medical, and biological research studies; providing online 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; providing online 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; providing online 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; providing online 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; providing online 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; providing online 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 for use in information management in the performance of a clinical trial; providing online non-downloadable software in the nature of a clinical trial management system for data processing and information management for use by academic medical centers and cancer centers; providing online non-downloadable software in the nature of a clinical trial management system for data processing and information management for use by clinical, medical, and biological research sites, site networks, hospitals, and health systems; providing online non-downloadable teaching software system in the nature of an e-learning apparatus support platform for content delivery, patient recruitment management, and learning process management and reporting for use by clinical, medical, and biological research site staff, study teams and patients relating to clinical trials; providing online non-downloadable software for patient identification for use by clinical, medical, and biological researchers for patients enrolled in clinical trials; providing online non-downloadable software for patient scheduling and tracking 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; business technology software consultation services regarding the implementation of computer software provided online for use in healthcare and research that is for the management and administration of research, the protection of research participants, and the automation and facilitation of the conduct of research studies and electronic consent of research participants; providing online education, namely, software as a service (SAAS) services featuring e-learning software for providing online courses of instruction relating to clinical trials in the field of medicine | 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 institutional biosafety committee services, namely, independent review and oversight of clinical trials involving genetically engineered gene therapy and vaccine research, specifically, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research; assessing the readiness of research sites to conduct gene therapy and vaccine research, namely, reviewing standards and practices to assure compliance with laws and regulations in the field of clinical trials involving human subjects; regulatory compliance consultation services in the nature of health inspection readiness and remediation in the field of clinical, medical, and biological research studies; consultation services in the field of pharmacovigilance strategies to ensure regulatory compliance and patient safety in the field of clinical trials involving human subjects; regulatory compliance consultation services in the field of informed consent protocols for clinical trial participants; consultation services in the field of research compliance, namely, regulatory compliance consultation services in the field of clinical trials involving human subjects

Downloadable electronic publications in the nature of articles, case studies, and e-learning modules in the field of clinical, medical, and biological research studies | Business consulting; business administrative assistance, namely, business support services for the preparation and filing of institutional biosafety committee and institutional review board forms for use in the field of human subject research; business management consultation services concerning organization transformation in the field of clinical trials involving human subjects; professional staffing services in the field of medical and scientific research; organizing and administering a network of research sites, namely, business consultation and management in the field of clinical trials, specifically, providing governmental registration assistance in the nature of regulatory submission management on behalf of research sites that conduct gene therapy and vaccine research to assist them with clinical research and clinical trials; providing institutional biosafety committee services, namely, providing independent review and oversight of clinical trials involving genetically engineered gene therapy and vaccine research for business purposes | Financial advisory services, namely, budget negotiation and budget set-up services in the field of clinical trials involving human subjects; insurance coverage consultancy services, namely, determining whether particular goods and services in clinical trials are covered by Medicare | Providing an on-line discussion platform and document sharing platform in the nature of an on-line forum for transmission of messages and information among computer 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; developing, arranging, and conducting educational conferences in the field of clinical, medical, and biological research studies; educational services, namely, providing online, non-downloadable webinars, seminars, and conferences in the field of clinical, medical, and biological research studies; non-downloadable 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; developing, arranging and conducting business conferences 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 in the nature of software as a service (SAAS) services featuring software for database management and information management 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 for use 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; providing institutional biosafety committee services, namely, review and oversight of clinical trials involving genetically engineered gene therapy and vaccine research, specifically, evaluating research sites involved in gene therapy and vaccine research clinical trials to determine whether the organizations conform to an established accreditation standard; assessing the readiness of research sites to conduct gene therapy and vaccine research, namely, testing, analysis, and evaluation of gene therapy and vaccine research service providers to determine conformity with established accreditation standards; consultation services in the nature of quality management, namely, quality evaluation and analysis, quality assurance, and quality control in the field of clinical, medical, and biological research studies; consultation services in the field of drug and medical device development; consultation services in the field of conducting clinical trials for others; consultation services in the field of scientific research compliance, namely, analysis and evaluation of scientific research of others in the field of clinical trials involving human subjects to assure compliance with industry standards; consultation services in the field of scientific research 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; consulting services in the field of medical and scientific research for clinical trials; providing online non-downloadable software for use by clinical, medical, and biological research study sponsors, contract research organizations, research sites, and research site staff for use in the design, administration, and tracking of clinical, medical, and biological research studies; providing online 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; providing online non-downloadable software for use in collecting and managing consents from participants in clinical, medical, and biological research studies; providing online 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; providing online 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; providing online 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; providing online 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; providing online 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; providing online 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 for use in information management in the performance of a clinical trial; providing online non-downloadable software in the nature of a clinical trial management system for data processing and information management for use by academic medical centers and cancer centers; providing online non-downloadable software in the nature of a clinical trial management system for data processing and information management for use by clinical, medical, and biological research sites, site networks, hospitals, and health systems; providing online non-downloadable teaching software system in the nature of an e-learning apparatus support platform for content delivery, patient recruitment management, and learning process management and reporting for use by clinical, medical, and biological research site staff, study teams and patients relating to clinical trials; providing online non-downloadable software for patient identification for use by clinical, medical, and biological researchers for patients enrolled in clinical trials; providing online non-downloadable software for patient scheduling and tracking 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; business technology software consultation services regarding the implementation of computer software provided online for use in healthcare and research that is for the management and administration of research, the protection of research participants, and the automation and facilitation of the conduct of research studies and electronic consent of research participants; providing online education, namely, software as a service (SAAS) services featuring e-learning software for providing online courses of instruction relating to clinical trials in the field of medicine | 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 institutional biosafety committee services, namely, independent review and oversight of clinical trials involving genetically engineered gene therapy and vaccine research, specifically, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research; assessing the readiness of research sites to conduct gene therapy and vaccine research, namely, reviewing standards and practices to assure compliance with laws and regulations in the field of clinical trials involving human subjects; regulatory compliance consultation services in the nature of health inspection readiness and remediation in the field of clinical, medical, and biological research studies; consultation services in the field of pharmacovigilance strategies to ensure regulatory compliance and patient safety in the field of clinical trials involving human subjects; regulatory compliance consultation services in the field of informed consent protocols for clinical trial participants; consultation services in the field of research compliance, namely, regulatory compliance consultation services in the field of clinical trials involving human subjects

Providing business information about the performance and availability of research sites and institutions for use by research sponsors and contract research organizations (CROs) | Providing information in the field of medical and scientific research; providing technological information about the performance and availability of research sites and institutions for use by research sponsors and contract research organizations (CROs)

Class 042: providing temporary use of non-downloadable cloud-based software for transmitting clinical trial data

"GENE THERAPY"

Business administrative assistance namely, business support services for the preparation and filing of institutional biosafety committee forms for use in the field of human subjects research

Providing temporary use of on-line non-downloadable software for use by 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; help desk support services for troubleshooting of computer software problems

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 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

Computer software for a support platform for use by site staff, study teams and patients in the performance of a clinical trial downloaded from the internet; computer software featuring e-learning solutions relating to clinical trials, downloaded from the internet; teaching apparatus in the nature of an e-learning apparatus support platform for use by site staff, study teams and patients relating to clinical trials | 44(e)) Distribution of data or audio visual images via a global computer network or the internet; Distribution of data or audio visual images, specifically e-learning solutions content relating to clinical trials, via a global computer network or the internet; streaming of video material on the internet; streaming of video material, specifically e-learning content relating to clinical trials, on the internet | Provision of education online, namely, providing online courses of instruction from a computer database or via the internet or extranet in the fields of clinical trials; provision of education online, namely, providing online courses of instruction, specifically e-learning solutions relating to clinical trials in the field of medicine, from a computer database or via the internet or extranet | 44(e)) Hosting of digital content on the internet; hosting of digital content, specifically e-learning solutions relating to clinical trials, on the internet; providing medical and scientific research in the field of pharmaceuticals and clinical trials

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

Regulatory compliance consulting services in the field of healthcare and research regarding providing regulatory and technology solutions for research studies and the protection of research participants in order to ensure regulatory compliance and efficient research operations; Technology consulting services in the field of healthcare and research regarding technology solutions for research studies and the protection of research participants in order to ensure regulatory compliance and efficient research study operations; 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 and facilitating the conduct of research studies, consent of research participants, and management of meetings where research studies are reviewed

Providing independent review of research involving human subjects, namely, reviewing protocols and related information to ensure protection of the rights and welfare of human subjects; regulatory compliance consulting services in the field of healthcare and research regarding regulatory for research studies and the protection of research participants in order to ensure regulatory compliance and efficient research study operations; Technology consulting services in the field of healthcare and research regarding technology solutions for research studies and the protection of research participants in order to ensure regulatory compliance and efficient research study operations; 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 and facilitating the conduct of research studies, consent of research participants, and management of meetings where research studies are reviewed

"CONSENT"; Technology consulting services regarding the implementation of computer software provided online for use in healthcare and research that is for the management and administration of research, the protection of research participants, and the automation and facilitation of the conduct of research studies and electronic consent of research participants; 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

"SITE"

"TRIAL"

[ 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 downloadable software for use by pharmaceutical companies and others in the design and administration of scientific and medical research projects and of clinical trials for pharmaceuticals, medical devices and medical procedures; Providing downloadable software for use by pharmaceutical companies and others in 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 | Managing databases for use by pharmaceutical companies and others in the design and administration of scientific and medical research projects, and of clinical trials for pharmaceuticals, medical devices and medical procedures; Managing databases for use by pharmaceutical companies and others in the 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 | Providing on-line non-downloadable software for use in design and administration of scientific and medical research projects, and of clinical trials for pharmaceuticals, medical devices and medical procedures; [ providing a website featuring non-downloadable software for use in the design and administration of scientific and medical research projects, and of clinical trials for pharmaceuticals, medical devices and medical procedures; ] Hosting, managing, developing, and maintaining [ web sites, ] software, and applications for use by pharmaceutical companies and others in the design and administration of scientific and medical research projects, and of clinical trials for pharmaceuticals, medical devices and medical procedures; Providing on-line non-downloadable software for use in 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, providing a website featuring non-downloadable software for use in 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; Hosting, managing, developing, and maintaining [ web sites, ] software, applications, and databases for use by pharmaceutical companies and others in 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; Providing on-line non-downloadable software for use by pharmaceutical companies and others in the tracking and management of patients, specimens, equipment, materials, funding, schedules, and performance milestones and metrics involved in scientific and medical research, and in clinical trials for pharmaceuticals, medical devices and medical procedures, providing a website featuring non-downloadable software for use by pharmaceutical companies and others in the tracking and management of patients, specimens, equipment, materials, funding, schedules, and performance milestones and metrics involved in scientific and medical research, and in clinical trials for pharmaceuticals, medical devices and medical procedures; Hosting, managing, developing, and maintaining [ web sites, ] software, and applications for use by pharmaceutical companies and others in the tracking and management of patients, specimens, equipment, materials, funding, schedules, and performance milestones and metrics involved in scientific and medical research, and in clinical trials for pharmaceuticals, medical devices and medical procedures; Providing on-line non-downloadable software for use by pharmaceutical companies and others in the monitoring and reporting of regulatory, standards, and safety compliance in scientific and medical research, and in clinical trials for pharmaceuticals, medical devices and medical procedures, providing a website featuring non-downloadable software for use by pharmaceutical companies and others in the monitoring and reporting of regulatory, standards, and safety compliance in scientific and medical research, and in clinical trials for pharmaceuticals, medical devices and medical procedures; Hosting, managing, developing, and maintaining [ web sites, ] software, and applications for use by pharmaceutical companies and others in the monitoring and reporting of regulatory, standards, and safety compliance in scientific and medical research, and in clinical trials for pharmaceuticals, medical devices and medical procedures; consulting services regarding all of the foregoing

"RESEARCH SYSTEMS"

"RESEARCH SYSTEMS"

"RESEARCH SYSTEMS"

Software as a service (SAAS) and application service provider (ASP) services, namely, providing, hosting, managing, developing, and maintaining software, applications, web sites, and databases for use by others in the design and administration of, and for data collection and data sharing in, scientific research projects, in the tracking and management of funding involved in scientific research, and in the monitoring and reporting of regulatory, standards, and safety compliance in scientific research

developing, arranging and conducting business conferences | developing, arranging and [ conduction ] * conducting * educational conferences

Software for the design and administration of clinical, medical, and biological research studies; software for the storage and analysis of data related to clinical, medical, and biological research samples; software for regulatory reporting, compliance tracking, and safety monitoring for clinical, medical, and biological research studies; software for financial accounting in clinical, medical, and biological research studies

Providing on-line forums, chat rooms and electronic bulletin boards for transmission of messages and information among users concerning oncology, cancer research, and general medical and health topics

Class 045: 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

Technology consultation in the field of engineering; consultation services in the fields of product research and development, and scientific research and development