ASCK
ASSIGNMENT OF OWNERSHIP NOT UPDATED AUTOMATICALLY
25/01/2023
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Dado oficial do USPTO
ADVARRA
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Active USPTO registrationTipo: VerbalEscritório: US
Snapshot rápido
ADVARRA
ST13
US500000097070782Classe
9, 35, 36, 38, 41, 42, 45
Pedido
97070782
Registro
6910756
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
21
Atualização mais recente
25/01/2023
Classificação
Registrada
Tipo de marca
Verbal
Classes Nice
9, 35, 36, 38, 41, 42, 45
Data de depósito
12/10/2021
Data de registro
29/11/2022
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
29/11/2022
Última transação
29/11/2022
Escritório responsável
United States Patent and Trademark Office
Código da situação
700
Cadastro oficial
Principal Register
Primeiro uso
31/12/2020
Primeiro uso no comércio
31/12/2020
Código do desenho
4
Tipo de titular
03
Localização do titular
Columbia, MD, US
Examinador
SMITH, TARYN E
Unidade examinadora
L40
Localização atual
PUBLICATION AND ISSUE SECTION
Titulares e representantes
Titulares
Advarra, Inc.
Representantes
Andrew J. Ferren GOULSTON & STORRS PC
Classificação técnica
Classes Nice
Classe 9Classe 35Classe 36Classe 38Classe 41Classe 42Classe 45
Códigos Vienna
Sem códigos Vienna disponíveis.
Produtos e serviços
Classe 9
Downloadable electronic publications in the nature of articlescase studiese-learning modules in the field of clinicalmedicalbiological research studies
Classe 35
Business consulting; business administrative assistancebusiness 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 sitesbusiness consultation and management in the field of clinical trialsspecificallyproviding 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 servicesproviding independent review and oversight of clinical trials involving genetically engineered gene therapy and vaccine research for business purposes
Classe 36
Financial advisory servicesbudget negotiation and budget set-up services in the field of clinical trials involving human subjects; insurance coverage consultancy servicesdetermining whether particular goods and services in clinical trials are covered by Medicare
Classe 38
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 oncologycancer researchgeneral medical and health topics
Classe 41
Providing online educationproviding online courses of instruction from a computer database or via the internet or extranet in the fields of clinical trials; developingarrangingconducting educational conferences in the field of clinicalmedicalbiological research studies; educational servicesproviding onlinenon-downloadable webinarsseminarsconferences in the field of clinicalmedicalbiological research studies; non-downloadable electronic publications in the nature of articlesblog postscase studiese-learning modules in the field of clinicalmedicalbiological research studies; developingarranging and conducting business conferences in the field of clinicalmedicalbiological research studies
Classe 42
Providing information in the field of medical and scientific research on the internet; providing digital contente-learning solutions in the nature of software as a service (SAAS) services featuring software for database management and information management relating to clinical trialson the internet; providing temporary use of on-line non-downloadable software for use by clinicalmedicalbiological researchersresearch sponsors and clinical research organizations for use in automating the submissionreview and approval process of human subject clinical research projects and providing access to forms and templates to researchersresearch sponsors and clinical research organizations for automating the submissionreview 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 servicesreview and oversight of clinical trials involving genetically engineered gene therapy and vaccine researchspecificallyevaluating 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 researchtestinganalysisevaluation of gene therapy and vaccine research service providers to determine conformity with established accreditation standards; consultation services in the nature of quality managementquality evaluation and analysisquality assurancequality control in the field of clinicalmedicalbiological 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 complianceanalysis 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 clinicalmedicalbiological research study sponsorscontract research organizationsresearch sitesresearch site staff for use in the designadministrationtracking of clinicalmedicalbiological research studies; providing online non-downloadable software for use by clinicalmedicalbiological research study sponsorscontract research organizationsresearch sitesresearch site staff in the storageanalysistransfer of data related to clinicalmedicalbiological research studies; providing online non-downloadable software for use in collecting and managing consents from participants in clinicalmedicalbiological research studies; providing online non-downloadable software for use by clinicalmedicalbiological research study sponsorscontract research organizationsresearch sitesresearch site staff in regulatory reportingcompliance trackingsafety monitoringevaluation of clinicalmedicalbiological research studies; providing online non-downloadable software enabling real-time communication for use by clinicalmedicalbiological research study sponsorscontract research organizationsresearch sitesresearch site staffinstitutional review boards in clinicalmedicalbiological research studies; providing online non-downloadable software for use by clinicalmedicalbiological research study sponsorscontract research organizationsresearch sitesresearch site staff in managing stipends and travel reimbursements in clinicalmedicalbiological research studies; providing online non-downloadable software for use by pharmaceutical companies and clinicalmedicalbiological research study sponsorscontract research organizations in the design and administration of scientific and medical research projects and of clinical trials for pharmaceuticalsmedical devices and medical procedures; providing online non-downloadable software for use by pharmaceutical companies and clinicalmedicalbiological research study sponsorscontract research organizationsresearch sitesresearch site staff for data collectiondata sharinginformation exchangecollaboration regarding scientific and medical research projects and regarding clinical trials for pharmaceuticalsmedical devices and medical procedures; providing online non-downloadable software in the nature of a support platform for use by clinicalmedicalbiological research study sponsorscontract research organizationsresearch sitesresearch site staffstudy 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 clinicalmedicalbiological research sitessite networkshospitalshealth systems; providing online non-downloadable teaching software system in the nature of an e-learning apparatus support platform for content deliverypatient recruitment managementlearning process management and reporting for use by clinicalmedicalbiological research site staffstudy teams and patients relating to clinical trials; providing online non-downloadable software for patient identification for use by clinicalmedicalbiological researchers for patients enrolled in clinical trials; providing online non-downloadable software for patient scheduling and tracking for use by clinicalmedicalbiological 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 researchthe protection of research participantsthe automation and facilitation of the conduct of research studies and electronic consent of research participants; providing online educationsoftware as a service (SAAS) services featuring e-learning software for providing online courses of instruction relating to clinical trials in the field of medicine
Classe 45
Providing regulatory compliance consultation services in the nature of advice concerning due diligencestrategic developmentregulatory policy in the field of clinical trials involving human subjects; 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; providing information relating to regulatory compliance for independent review of clinical trials involving human subjects; providing institutional biosafety committee servicesindependent review and oversight of clinical trials involving genetically engineered gene therapy and vaccine researchspecificallyreviewing 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 researchreviewing 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 clinicalmedicalbiological 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 complianceregulatory compliance consultation services in the field of clinical trials involving human subjects
Publicações
Histórico de despachos e eventos da marca no USPTO.
21 publicações encontradas
NRCC
NOTICE OF REGISTRATION CONFIRMATION EMAILED
29/11/2022
R.PR
REGISTERED-PRINCIPAL REGISTER
29/11/2022
ASCK
ASSIGNMENT OF OWNERSHIP NOT UPDATED AUTOMATICALLY
02/11/2022
NPUB
OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED
13/09/2022
PUBO
PUBLISHED FOR OPPOSITION
13/09/2022
NONP
NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED
24/08/2022
CNSA
APPROVED FOR PUB - PRINCIPAL REGISTER
09/08/2022
XAEC
EXAMINER'S AMENDMENT ENTERED
09/08/2022
GNEN
NOTIFICATION OF EXAMINERS AMENDMENT E-MAILED
09/08/2022
GNEA
EXAMINERS AMENDMENT E-MAILED
09/08/2022
CNEA
EXAMINERS AMENDMENT -WRITTEN
09/08/2022
TEME
TEAS/EMAIL CORRESPONDENCE ENTERED
29/07/2022
CRFA
CORRESPONDENCE RECEIVED IN LAW OFFICE
29/07/2022
TROA
TEAS RESPONSE TO OFFICE ACTION RECEIVED
29/07/2022
GNRN
NOTIFICATION OF NON-FINAL ACTION E-MAILED
14/02/2022
GNRT
NON-FINAL ACTION E-MAILED
14/02/2022
CNRT
NON-FINAL ACTION WRITTEN
14/02/2022
DOCK
ASSIGNED TO EXAMINER
23/12/2021
NWOS
NEW APPLICATION OFFICE SUPPLIED DATA ENTERED
02/11/2021
NWAP
NEW APPLICATION ENTERED
15/10/2021
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