Mark:

WCG

Status Date:

02-09-2024

Registration Number:

N/A

Goods and Services:

Training services in the field of clinical trials; training in the field of testing protocols designed to evaluate the abuse potential of pharmaceuticals during clinical testing or general clinical practice; training of clinical professionals; training services to be delivered to participants involved in conducting clinical trials in the medical and pharmaceutical industries; providing online learning management services for training and compliance within the research professionals including highly-specialized areas of training in clinical research; services for arranging and conducting seminars designed to inform potential candidates about clinical trials or new health care products being marketed directly to patients; scientific research in the nature of evaluation and monitoring, namely, assisting and facilitating clinical trials for others; 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 Administration, billing and reconciliation of accounts for clinical trial site; financial management of reimbursement payment for clinical trial sites; and financial management in the field of clinical trials, including accounts receivable 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 Advertising, promotion, and marketing services in the nature of customized internal and publicly presented digital and traditional media for health providers, including dental and veterinary practices, clinical research trial sites, pharmaceutical trial sponsors and contract research organizations; recruitment advertisement services, namely, posting of clinical trial notices for the purpose of recruiting patients for participation in clinical trials for the testing of drugs; market research services; design of recruitment advertising materials for others for clinical trials; patient marketing programs services for others in the medical and pharmaceutical fields; market research services for customizing selection of patients for clinical trials; support for administrative procedures with descriptions of consent to participants in clinical trials; assistance for administrative procedures with schedule management of examination participants' visits and examinations, clinical investigators, clinical participants, and pharmacies; support for administrative procedures with communication coordination between the nursing department, the examination department, the medical department, 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, developing coverage analyses, negotiating clinical trial budgets and contracts on behalf of research sites, financial management, Clinical Trial Management System (CTMS) implementation and management, and staff training as it relates to any of the foregoing; 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 negotiate study budgets for clinical trial sites; business consulting in the field of clinical trial study identification on behalf of clinical trial sites; business consulting in the field of clinical trials, namely, negotiating clinical trial budgets and business contracts on behalf of clinical trial sites; spoke fluent of business contracts for third, supported by technology-driven processes and an international network of attorneys who know about specific, in-depth local and regulations; providing the services of identifying and choosing the clinical trial and an electronic document management system to collect, manage, store, and facilitate the documents for such site identification; 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; 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; 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; negotiating clinical trial contracts and budgets between biopharmaceutical companies, contract research organizations and investigator sites around the world 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; offering a variety of global contract negotiation resource placement, supported by technology-driven processes and a network of international attorneys who possess specialized, in-depth knowledge of local languages and regulations Evaluation and diagnostic services in the field of reviewing 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 patient retention services for retaining patients 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 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; consulting services in the field of compliance with international and federal regulations and guidelines relating to clinical studies involving humans and informed consent; technical consulting in the field of clinical trials for the testing of drugs, biologics, and medical devices; providing information regarding drug clinical trials and related matters; management and compilation of secure computer databases of patient medical information; 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 in conducting an informed consent process tailored for helping such sites deliver robust and accurate information to potential patients by providing accessible and consistent institutional review board (IRB) and clinical trial sponsor approved messages, and empowering patients to make informed decisions regarding their participation in clinical studies; Providing a web site featuring technology enabling others 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 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 services in support of clinical trial start-up and management, namely, developing and managing 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; 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 related information services to prospective or current clinical trial participants to increase engagement and retention in clinical trials via telephone and email; providing scientific research related information services to prospective or current clinical trial participants for clinical assistance and quality assurance purposes to increase rater reliability in trials where subjective scales are relied upon to improve rating consistency and trial efficacy

Class:

Legal services

Published for Opposition Date:

N/A

Mark Drawing Status:

4

Business Name:

620 EIGHTH AVENUE