EWAF
TEAS WITHDRAWAL OF ATTORNEY RECEIVED-FIRM RETAINS
07/05/2025
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Dado oficial do USPTO
FORMEDIX RYZE
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Active USPTO registrationTipo: VerbalEscritório: US
Snapshot rápido
FORMEDIX RYZE
ST13
US500000090132747Classe
35, 41, 42
Pedido
90132747
Registro
6482181
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
37
Atualização mais recente
14/05/2025
Classificação
Registrada
Tipo de marca
Verbal
Classes Nice
35, 41, 42
Data de depósito
24/08/2020
Data de registro
14/09/2021
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
14/09/2021
Última transação
14/05/2025
Escritório responsável
United States Patent and Trademark Office
Código da situação
700
Cadastro oficial
Principal Register
Fundamento do pedido
Foreign priority
Código do desenho
4
Tipo de titular
99
Localização do titular
Glasgow, SC
Examinador
BURCH,JILLIAN RENEE
Unidade examinadora
O10
Localização atual
PUBLICATION AND ISSUE SECTION
Titulares e representantes
Titulares
Formedix Limited
Formedix Limited
Representantes
Carrie Webb Olson DAY PITNEY LLP
Classificação técnica
Classes Nice
Classe 35Classe 41Classe 42
Códigos Vienna
Sem códigos Vienna disponíveis.
Produtos e serviços
Classe 35
On-line retail ordering services featuring clinical metadata management computer software for use in relation to clinical trialsclinical management computer software for use in relation to clinical trialscomputer software for use in exclusively collectingstoringcontrollingmanaging and submitting of clinical metadata and clinical data in relation to clinical trialsdatabase management computer software for use exclusively in relation to clinical trialscomputer software to allow users to collectstorecontrolmanage and submit clinical metadata and clinical data in relation to clinical trialscomputer databases for collectingstoringcontrollingmanaging and submitting clinical data in relation to clinical trialscomputer software designed to ensure that clinical metadata and clinical data meets the regulations and standards required by international and government agencies in relation to clinical trialscomputer software used by pharmaceutical companiesbiotechnology companiesmedical device manufacturerscontract research organizations to help collect the required clinical data and meet the required standards for data collectiontabulationanalysissubmission for clinical trialsall of the aforesaid computer software being used in relation to clinical trials only
Classe 41
Providing training services to enable pharmaceutical companiesbiotechnology companiesmedical device manufacturerscontract research organizations to use clinical metadata management software platforms for managing clinical trial metadata and clinical trial data; providing training services to enable pharmaceutical companiesbiotechnology companiesmedical device manufacturerscontract research organizations to collect the required clinical data and meet the regulations and standards required by international and government agencies for data collectiontabulationanalysissubmission for clinical trials; providing training services in relation to the use of clinical metadata management computer software for use in relation to clinical trials; providing training services in relation to the use of clinical management computer software for use in relation to clinical trials; all of the aforesaid training services being used in relation to clinical trials only
Classe 42
Providing temporary use of on-line non-downloadable clinical metadata management computer software for use in relation to clinical trials; providing temporary use of on-line non-downloadable clinical management computer software for use in relation to clinical trials; providing temporary use of on-line non-downloadable computer software for use in exclusively collectingstoringcontrollingmanaging and submitting of clinical metadata and clinical data in relation to clinical trials; providing temporary use of on-line non-downloadable database management computer software for use exclusively in relation to clinical trials; providing temporary use of on-line non-downloadable computer software to allow users to collectstorecontrolmanage and submit clinical metadata and clinical data in relation to clinical trials; providing on-line computer databases for collectingstoringcontrollingmanaging and submitting clinical data in relation to clinical trials; providing temporary use of on-line non-downloadable computer software designed to ensure that clinical metadata and clinical data meets the regulations and standards required by international and government agencies in relation to clinical trials; providing temporary use of on-line non-downloadable computer software used by pharmaceutical companiesbiotechnology companiesmedical device manufacturerscontract research organizations to help collect the required clinical data and meet the required standards for data collectiontabulationanalysissubmission for clinical trials; design and development of computer software exclusively for managing clinical metadata and clinical data in clinical trials; designingcreating and maintaining web pages exclusively in connection with collectingstoringcontrolling and managing clinical metadata and clinical datato meet the regulations and standards required by international and government agencies in conducting clinical trials; all of the aforesaid software services being used in relation to clinical trials only; technical support servicestroubleshooting of computer software problems related to clinical metadata management software platforms for managing clinical trial metadata and clinical trial data; providing medical and scientific research information in the field of clinical trials to enable pharmaceutical companiesbiotechnology companiesmedical device manufacturerscontract research organizations to collect the required clinical data and meet the regulations and standards required by international and government agencies for data collectiontabulationanalysissubmission for clinical trials; technical support servicestroubleshooting of computer software problems related to clinical metadata management computer software for use in relation to clinical trials; technical support servicestroubleshooting of computer software problems related to clinical management computer software for use in relation to clinical trials; all of the aforesaid information and support services being used in relation to clinical trials only
Publicações
Histórico de despachos e eventos da marca no USPTO.
37 publicações encontradas
TCCA
TEAS CHANGE OF CORRESPONDENCE RECEIVED
07/05/2025
ECDR
TEAS CHANGE OF DOMESTIC REPRESENTATIVES ADDRESS
07/05/2025
ARAA
ATTORNEY/DOM.REP.REVOKED AND/OR APPOINTED
07/05/2025
REAP
TEAS REVOKE/APP/CHANGE ADDR OF ATTY/DOM REP RECEIVED
07/05/2025
CHAN
APPLICANT/CORRESPONDENCE CHANGES (NON-RESPONSIVE) ENTERED
07/05/2025
COAR
TEAS CHANGE OF OWNER ADDRESS RECEIVED
07/05/2025
R.PR
REGISTERED-PRINCIPAL REGISTER
14/09/2021
DP1B
1(B) BASIS DELETED; PROCEED TO REGISTRATION
12/08/2021
AITU
CASE ASSIGNED TO INTENT TO USE PARALEGAL
12/08/2021
IUCN
NOTICE OF ALLOWANCE CANCELLED
03/08/2021
D1BR
TEAS DELETE 1(B) BASIS RECEIVED
03/08/2021
NOAM
NOA E-MAILED - SOU REQUIRED FROM APPLICANT
27/07/2021
NPUB
OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED
01/06/2021
PUBO
PUBLISHED FOR OPPOSITION
01/06/2021
NONP
NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED
12/05/2021
CNSA
APPROVED FOR PUB - PRINCIPAL REGISTER
23/04/2021
TEME
TEAS/EMAIL CORRESPONDENCE ENTERED
22/04/2021
CRFA
CORRESPONDENCE RECEIVED IN LAW OFFICE
22/04/2021
ERFR
TEAS REQUEST FOR RECONSIDERATION RECEIVED
22/04/2021
GNFN
NOTIFICATION OF FINAL REFUSAL EMAILED
20/04/2021
GNFR
FINAL REFUSAL E-MAILED
20/04/2021
CNFR
FINAL REFUSAL WRITTEN
20/04/2021
AMPX
PRELIMINARY/VOLUNTARY AMENDMENT - ENTERED
29/03/2021
PARI
TEAS VOLUNTARY AMENDMENT RECEIVED
29/03/2021
TEME
TEAS/EMAIL CORRESPONDENCE ENTERED
09/03/2021
CRFA
CORRESPONDENCE RECEIVED IN LAW OFFICE
09/03/2021
TROA
TEAS RESPONSE TO OFFICE ACTION RECEIVED
03/03/2021
GNRN
NOTIFICATION OF NON-FINAL ACTION E-MAILED
22/12/2020
GNRT
NON-FINAL ACTION E-MAILED
22/12/2020
CNRT
NON-FINAL ACTION WRITTEN
22/12/2020
DOCK
ASSIGNED TO EXAMINER
21/12/2020
AMPX
PRELIMINARY/VOLUNTARY AMENDMENT - ENTERED
02/12/2020
ALIE
ASSIGNED TO LIE
30/11/2020
NWOS
NEW APPLICATION OFFICE SUPPLIED DATA ENTERED
25/09/2020
PARI
TEAS VOLUNTARY AMENDMENT RECEIVED
14/09/2020
NWAP
NEW APPLICATION ENTERED
27/08/2020
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