WCG CLINICAL INC.

platform as a service (PaaS) services featuring computer software platforms to enable users to conduct and manage clinical trials, namely, software to capture, manage, analyzing and store clinical data, materials, and documents

platform as a service (PaaS) services featuring computer software platforms to enable users to conduct and manage clinical trials, namely, software to capture, manage, analyzing and store clinical data, materials, and documents

training and educational services in the clinical trial industry, namely, medical training; Medical training of clinical professionals; arranging and conducting of educational conferences in the field of clinic trials; Educational services, namely, providing online learning management courses services in the field of clinical trial research training and compliance; providing safety and ethics instruction in the field of scientific clinical trials to the officials within the research site who oversee the human subjects during research; financial management in the clinical trial industry; patient recruitment services in the clinical trial industry; business consulting, management, and planning services in the clinical trial industry; collecting and providing statistical analysis of clinical trial data for business purposes; patient relationship management services, namely, providing patient retention services for retaining patients in clinical trials; all the foregoing relating to the clinical trial industry; 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; Regulatory compliance consulting in the field of clinical trials and life sciences research, namely, providing consultation to develop a corrective action plan for research misconduct or issues of noncompliance; conducting medical physical evaluation and medical diagnostic testing, monitoring and reporting services for patients participating in clinical trials; providing an online database featuring healthcare research information; "CLINICAL"; consulting services for others in the field of design, planning, and implementation project management of clinical trials; technical consulting in the design, planning, and implementation project management of clinic trials; providing consulting in the development of quality control standards for clinical trials and life sciences research in the field of clinical trials; Scientific research, namely, collecting and providing statistical analysis of clinical trial data for clinical research purposes; design, development, implementation, management, and maintenance of software, and software as a service (SaaS) for others in the clinical trial industry; design, development, implementation, and configuration management of computer hardware for others in the clinical trial industry; providing website platforms for the clinical trial industry, namely, providing a web hosting platform for medical professionals in the clinical trial industry; conducting scientific feasibility studies for clinical trials; providing scientific research information to prospective or current clinical trial participants; scientific research in the nature of evaluation and monitoring, namely, assisting and facilitating clinical trials for others

training and educational services in the clinical trial industry, namely, medical training; Medical training of clinical professionals; arranging and conducting of educational conferences in the field of clinic trials; Educational services, namely, providing online learning management courses services in the field of clinical trial research training and compliance; providing safety and ethics instruction in the field of scientific clinical trials to the officials within the research site who oversee the human subjects during research; financial management in the clinical trial industry; Patient recruitment services in the clinical trial industry; business consulting, management, and planning services in the clinical trial industry; collecting and providing statistical analysis of clinical trial data for business purposes; patient relationship management services, namely, providing patient retention services for retaining patients in clinical trials; all the foregoing relating to the clinical trial industry; 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; Regulatory compliance consulting in the field of clinical trials and life sciences research, namely, providing consultation to develop a corrective action plan for research misconduct or issues of noncompliance; Conducting medical physical evaluation and medical diagnostic testing, monitoring and reporting services for patients participating in clinical trials; providing an online database featuring healthcare research information; consulting services for others in the field of design, planning, and implementation project management of clinical trials; technical consulting in the design, planning, and implementation project management of clinical trials; providing consulting in the development of quality control standards for clinical trials and life sciences research in the field of clinical trials; Scientific research, namely, collecting and providing statistical analysis of clinical trial data for clinical research purposes; design, development, implementation, management, and maintenance of software, and software as a service (SaaS), for others in the clinical trial industry; design, development, implementation, and configuration management of computer hardware for others in the clinical trial industry; providing website platforms for the clinical trial industry, namely, providing a web hosting platform for medical professionals in the clinical trial industry; conducting scientific feasibility studies for clinical trials; providing scientific research information to prospective or current clinical trial participants; scientific research in the nature of evaluation and monitoring, namely, assisting and facilitating clinical trials for others

Training services in the field of clinical trials; training in the field of pharmaceutical testing relating to training on tested protocols designed to evaluate the abuse potential of pharmaceuticals during clinical testing or general clinical practice; Medical training of clinical professionals; training services to be delivered to participants involved in conducting clinical trials in the medical and pharmaceutical industries; Educational services, namely, providing online learning management courses and highly-specialized training for research professionals in the field of clinical trial research training and compliance; arranging and conducting seminars to prospective clinical trial participants about clinical trials research; providing safety instruction in the field of scientific clinical trials to the officials within the research site who oversee the human subjects during research; staff training, namely, business training for others in the field of clinical trial research; financial management of reimbursement payment for other clinical trial sites; financial management in the field of clinical trials, namely, accounts receivables financing and accounts payable debiting, for clinical trial sites; executing and tracking payments from the research sponsor to its associated research sites for payment for research studies; Financial advisory services, namely, budget negotiation in the field of clinical trials; Financial advisory services, namely, budget negotiation in the field of clinical trials, namely, between biopharmaceutical companies, contract research organizations and investigator sites around the world; providing business administrative procedure services for obtaining descriptions of participants' consents in clinical trials; business assistance for administrative procedures with schedule management of examination participants' visits and examinations, clinical investigators, and clinical participants; providing business administrative assistance for the creation and preservation of clinical trial documents and records related to the trial implementation plan, case report, substitute for recruitment of subjects; Business consulting, management, and planning services in the field of clinical trials, namely, cost analyses of patient insurance coverage for businesses, negotiating business contracts on behalf of research sites; business consulting, management, and planning services in the field of clinical trials, namely, analyzing and reporting possible cost savings in human research study protocol development and possible cost savings in research site identification on behalf of pharmaceutical trial sponsors and contract research organizations, all for business cost management purposes; business consulting, management, and planning services in the field of clinical trials, namely, applying business analytics to determine the appropriate payer coverage and for use in assisting with study budget negotiations for clinical trial sites; business consulting in the field of clinical trial study identification on behalf of clinical trial sites, namely, negotiating business contracts on behalf of clinical trial sites; business consulting in the field of clinical trials, namely, negotiating business contracts on behalf of clinical trial sites; business consulting and management in the field of clinical trials, namely, providing information management services; Business services, namely, formulation of best practices for clinical trial execution and management for the testing of drugs, biologics, and medical devices; management of telephone call centers for others; preparation of business reports related to key trends and innovations in clinical trial execution and management for the testing of drugs, biologics, and medical devices; Professional staffing services and staff management of institutional review boards, institutional biosafety committees and conflicts of interest; providing business administrative assistance to the officials within the research site who oversee the human subjects research; negotiating clinical trial business contracts between biopharmaceutical companies, contract research organizations and investigator sites around the world; Administration, billing and reconciliation of accounts on behalf of other clinical trial sites; providing patient retention services for retaining patients in clinical trials; Management and compilation of secure computerised databases of patient medical information; 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; Regulatory compliance consulting in the field of clinical trials and life sciences research, namely, providing consultation to develop a corrective action plan for research misconduct or issues of noncompliance; legal assistance in the drawing up of global contracts for others for resource placement, supported by technology-driven processes and a network of international attorneys who possess specialized, in-depth knowledge of local languages and regulations; Legal assistance in the drawing up of contracts and legal services in relation to the negotiation of contracts for others, all supported by technology-driven processes and an international network of attorneys who know about specific, in-depth local and regulations; Consulting services in the field of international and federal regulatory compliance requirements and guidelines for personnel safety relating to the protection of the rights and welfare of human subjects of clinical research studies; Medical evaluation of and medical diagnostic services for potential clinical trial patients with arthritic-based issues; medical evaluation and medical diagnostic testing, monitoring and reporting services of patients with arthritic-based issues for potential participation in clinical trials; providing an on-line database featuring healthcare research information; Consulting services for others in the field of implementation project management of testing research protocols designed to evaluate the abuse potential of pharmaceuticals during clinical testing or general clinical practice and the analysis of those results; clinical research consulting and advisory services related to ensuring the safety of pharmaceutical preparations administered to patients during clinical trials; collecting and providing statistical analysis of clinical trial data for clinical research purposes; technical consulting in the field of clinical research trials for the testing of drugs, biologics, and medical devices; providing information on drug clinical trials; Providing online non-downloadable computer software to manage health care research and support information through the Internet; providing temporary use of online non-downloadable software for use in assisting clinical trial sites, namely, providing temporary use of online non-downloadable software for conducting informed patient consent processes and featuring technology that enables potential patient users to access consistent institutional review board (IRB) and clinical trial sponsor approved messages, which helps potential patients make informed decisions regarding their participation in clinical studies; Providing a web site featuring technology enabling internet users to manage and exchange healthcare research information; providing consultation in the development and maintenance of standards required to meet accreditation by others in the field of clinical trials involving human subjects and research protocols relating to same; Scientific study and research in the field of clinical research, namely, providing scientific review of human subjects research protocols as to the design and risks involved; providing computer services in support of clinical trial start-up and management, namely, developing and hosting a web-accessed technology platform used for facilitating communication between clinical trial sponsors, contract research organizations, and clinical trial sites; providing a website featuring technology that enables users to collect, manage and share documents to facilitate communication during clinical trials; Providing temporary use of on-line non-downloadable software for conducting assessment surveys regarding suitability for site participation in clinical trials and utilizing data analytics to select appropriate clinical trial site locations; providing online non-downloadable software for posting, tracking, and accessing reports related to clinical training courses attended by clinical trial clinicians; providing scientific research information services, in the field of clinical trials, to prospective or current clinical trial participants, all for the purpose of increasing participant engagement and retention in clinical trials, and provided via telephone and e-mail; providing scientific research information services, in the field of clinical trials, to prospective or current clinical trial participants, all for clinical assistance and quality assurance purposes, and to increase rater reliability in trials where subjective scales are relied upon to improve rating consistency and trial efficacy; Providing on-line non-downloadable software for executing and tracking payments from the research sponsor to its associated research sites for payment for research studies; scientific research in the nature of evaluation and monitoring, namely, assisting and facilitating clinical trials for others; Graphic design of recruitment advertising materials for others for clinical trials; Implementing and managing enterprise system software applications in the nature of Clinical Trial Management System (CTMS)

Business consulting and management in the field of clinical trials, namely, providing information management services; formulation of best practices for clinical trial execution and management for the testing of drugs, biologics, and medical devices; preparation of business reports related to key trends and innovations in clinical trial execution and management for the testing of drugs, biologics, and medical devices; conducting conferences in the fields of clinical trials for the testing of drugs, biologics, and medical devices for business purposes; association services, namely, promoting the interests of the clinical trial field | Conducting seminars in the fields of clinical trials for the testing of drugs, biologics, and medical devices; conducting educational programs, presentations, conferences and seminars in the fields of clinical trials for the testing of drugs, biologics, and medical devices; Educational services, namely, providing on-line business training, courses and seminars in the field of clinical trials for the testing of drugs, biologics, and medical devices | Technical consulting in the field of clinical trials for the testing of drugs, biologics, and medical devices; consulting services in the fields of research and development for drugs, biologics, and medical devices

Class 042: Providing a web site featuring technology for use by others to manage and exchange healthcare research information; providing use of non-downloadable computer software via the internet for managing healthcare research and support information; services in the field of compliance with international and federal regulations and guidelines in the nature of development of quality control standards relating to clinical studies involving humans and informed consent; Providing an on-line database featuring healthcare in the nature of medical research information; Class 044: Providing an on-line database featuring healthcare research information; 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; reviewing the safety and ethics of research protocols for bio-pharmaceutical and medical device testing on humans, namely, investigating testing procedures, staff qualifications and consent forms; reviewing standards and practices to assure regulatory compliance with international and federal regulations relating to clinical studies involving humans and informed consent

Class 042: Providing a web site featuring technology for use by others to manage and exchange healthcare research information; providing use of non-downloadable computer software via the internet for managing healthcare research and support information; services in the field of compliance with international and federal regulations and guidelines in the nature of development of quality control standards relating to clinical studies involving humans and informed consent; Providing an on-line database featuring healthcare in the nature of medical research information; Class 044: Providing an on-line database featuring healthcare research information; 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; reviewing the safety and ethics of research protocols for bio-pharmaceutical and medical device testing on humans, namely, investigating testing procedures, staff qualifications and consent forms; reviewing standards and practices to assure regulatory compliance with international and federal regulations relating to clinical studies involving humans and informed consent

Class 042: Providing a web site featuring technology for use by others to manage and exchange healthcare research information; providing use of non-downloadable computer software via the internet for managing healthcare research and support information; providing an on-line database featuring healthcare in the nature of medical research information; Class 044: Providing an on-line database featuring healthcare research information

Class 042: Providing a web site featuring technology for use by others to manage and exchange healthcare research information; providing use of non-downloadable computer software via the internet for managing healthcare research and support information; providing an on-line database featuring healthcare in the nature of medical research information; Class 044: Providing an on-line database featuring healthcare research information

"GLOBAL"

providing instruction in the field of safety and ethics to the officials within the research site who oversee the human subjects research; staffing and management of institutional review boards, institutional biosafety committees and conflicts of interest; providing administrative support to the officials within the research site who oversee the human subjects research; 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 consultation to develop a corrective action plan for research misconduct or issues of noncompliance; providing an on-line database featuring healthcare research information; "GROUP"; providing a web site featuring technology enabling others to manage and exchange healthcare research information; providing use of non-downloadable computer software via the internet for managing healthcare research and support information; providing consultation in the development and maintenance of standards required to meet accreditation by others in the field of clinical trials involving human subjects and research protocols relating to same; scientific writing and editing of research protocols for others involved in human subjects research; developing research protocols for others involved in human subjects research; providing scientific review of human subjects research protocols as to the merit, design and risks involved

providing information in the field of clinical medical research to support the design, distribution and review of research protocols and guidelines