NRCC
NOTICE OF REGISTRATION CONFIRMATION EMAILED
24/02/2026
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Dado oficial do USPTO
WCG
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Active USPTO registrationTipo: VerbalEscritório: US
Snapshot rápido
WCG
ST13
US500000097922801Classe
35, 36, 41, 42, 44, 45
Pedido
97922801
Registro
8152462
Diagnóstico de risco e oportunidade
Leitura executiva para decisão de naming, protocolo e monitoramento.
Situação USPTO
Active USPTO registration
Tipo de processo
Pedido e registro
Eventos registrados
28
Atualização mais recente
25/02/2026
Classificação
Registrada
Tipo de marca
Verbal
Classes Nice
35, 36, 41, 42, 44, 45
Data de depósito
05/05/2023
Data de registro
24/02/2026
Data de expiração
-
Ação recomendada
Execute uma análise de colidência completa e valide classes antes de qualquer protocolo ou investimento de marca.
Próximo passo
Esses são os detalhes do processo de registro. Mesmo assim, o monitoramento constante é o que garante tranquilidade de que o seu principal ativo continue protegido.
Dados completos do processo
Campos estruturados da autoridade responsável e do histórico oficial.
Data da situação
24/02/2026
Última transação
25/02/2026
Escritório responsável
United States Patent and Trademark Office
Código da situação
700
Cadastro oficial
Principal Register
Fundamento do pedido
Intent to use
Primeiro uso
12/06/2023
Primeiro uso no comércio
12/06/2023
Código do desenho
4
Tipo de titular
03
Localização do titular
Princeton, NJ, US
Examinador
MACDOUGALL, KIERRA RYNNE
Unidade examinadora
N80
Localização atual
PUBLICATION AND ISSUE SECTION
Titulares e representantes
Titulares
WCG Clinical Inc.
Representantes
Jessica L. Rothstein GOODWIN PROCTER LLP
Classificação técnica
Classes Nice
Classe 35Classe 36Classe 41Classe 42Classe 44Classe 45
Códigos Vienna
Sem códigos Vienna disponíveis.
Produtos e serviços
Classe 35
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 examinationsclinical investigatorsclinical participants; providing business administrative assistance for the creation and preservation of clinical trial documents and records related to the trial implementation plancase reportsubstitute for recruitment of subjects; Business consultingmanagementplanning services in the field of clinical trialscost analyses of patient insurance coverage for businessesnegotiating business contracts on behalf of research sites; business consultingmanagementplanning services in the field of clinical trialsanalyzing 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 organizationsall for business cost management purposes; business consultingmanagementplanning services in the field of clinical trialsapplying 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 sitesnegotiating business contracts on behalf of clinical trial sites; business consulting in the field of clinical trialsnegotiating business contracts on behalf of clinical trial sites; business consulting and management in the field of clinical trialsproviding information management services; Business servicesformulation of best practices for clinical trial execution and management for the testing of drugsbiologicsmedical 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 drugsbiologicsmedical devices; Professional staffing services and staff management of institutional review boardsinstitutional 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 companiescontract research organizations and investigator sites around the world; Administrationbilling 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
Classe 36
financial management of reimbursement payment for other clinical trial sites; financial management in the field of clinical trialsaccounts receivables financing and accounts payable debitingfor clinical trial sites; executing and tracking payments from the research sponsor to its associated research sites for payment for research studies; Financial advisory servicesbudget negotiation in the field of clinical trials; Financial advisory servicesbudget negotiation in the field of clinical trialsbetween biopharmaceutical companiescontract research organizations and investigator sites around the world
Classe 41
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 servicesproviding 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 trainingbusiness training for others in the field of clinical trial research
Classe 42
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 drugsbiologicsmedical 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 sitesproviding 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 messageswhich 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 researchproviding 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 managementdeveloping and hosting a web-accessed technology platform used for facilitating communication between clinical trial sponsorscontract research organizationsclinical trial sites; providing a website featuring technology that enables users to collectmanage 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 postingtrackingaccessing reports related to clinical training courses attended by clinical trial clinicians; providing scientific research information servicesin the field of clinical trialsto prospective or current clinical trial participantsall for the purpose of increasing participant engagement and retention in clinical trialsprovided via telephone and e-mail; providing scientific research information servicesin the field of clinical trialsto prospective or current clinical trial participantsall for clinical assistance and quality assurance purposesto 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 monitoringassisting 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)
Classe 44
Medical evaluation of and medical diagnostic services for potential clinical trial patients with arthritic-based issues; medical evaluation and medical diagnostic testingmonitoring and reporting services of patients with arthritic-based issues for potential participation in clinical trials; providing an on-line database featuring healthcare research information
Classe 45
Providing independent review of clinical trials involving human subjectsreviewing 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 researchproviding 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 placementsupported by technology-driven processes and a network of international attorneys who possess specializedin-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 othersall supported by technology-driven processes and an international network of attorneys who know about specificin-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
Publicações
Histórico de despachos e eventos da marca no USPTO.
28 publicações encontradas
R.PR
REGISTERED-PRINCIPAL REGISTER
24/02/2026
SUNA
NOTICE OF ACCEPTANCE OF STATEMENT OF USE E-MAILED
30/01/2026
CNPR
ALLOWED PRINCIPAL REGISTER - SOU ACCEPTED
30/01/2026
SUPC
STATEMENT OF USE PROCESSING COMPLETE
07/10/2025
EXRA
NOTICE OF APPROVAL OF EXTENSION REQUEST E-MAILED
15/09/2025
IUAF
USE AMENDMENT FILED
10/06/2025
EISU
TEAS STATEMENT OF USE RECEIVED
10/06/2025
EX1G
SOU EXTENSION 1 GRANTED
10/06/2025
EXT1
SOU EXTENSION 1 FILED
10/06/2025
EEXT
SOU TEAS EXTENSION RECEIVED
10/06/2025
NOAM
NOA E-MAILED - SOU REQUIRED FROM APPLICANT
10/12/2024
NPUB
OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED
29/10/2024
PUBO
PUBLISHED FOR OPPOSITION
29/10/2024
NONP
NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED
09/10/2024
CNSA
APPROVED FOR PUB - PRINCIPAL REGISTER
21/09/2024
TEME
TEAS/EMAIL CORRESPONDENCE ENTERED
30/07/2024
CRFA
CORRESPONDENCE RECEIVED IN LAW OFFICE
30/07/2024
TROA
TEAS RESPONSE TO OFFICE ACTION RECEIVED
30/07/2024
ASCK
ASSIGNMENT OF OWNERSHIP NOT UPDATED AUTOMATICALLY
20/06/2024
XELG
APPLICATION EXTENSION GRANTED/RECEIPT PROVIDED
24/04/2024
XELR
APPLICATION EXTENSION TO RESPONSE PERIOD - RECEIVED
24/04/2024
GNRN
NOTIFICATION OF NON-FINAL ACTION E-MAILED
09/02/2024
GNRT
NON-FINAL ACTION E-MAILED
09/02/2024
CNRT
NON-FINAL ACTION WRITTEN
09/02/2024
DOCK
ASSIGNED TO EXAMINER
31/01/2024
NWOS
NEW APPLICATION OFFICE SUPPLIED DATA ENTERED
05/06/2023
NWAP
NEW APPLICATION ENTERED
09/05/2023
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