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Dado oficial do USPTO

A

Sabia que essa marca já está registrada no Estados Unidos?

Antes de investir em nome, identidade e divulgação, valide risco de colisão e estratégia de registro para não perder tempo nem budget.

Active USPTO registrationTipo: MistaEscritório: US

Snapshot rápido

A

ST13

US500000097915043

Classe

35, 42, 45

Pedido

97915043

Registro

7391557

Diagnóstico de risco e oportunidade

Leitura executiva para decisão de naming, protocolo e monitoramento.

Atenção: há risco ativo

Situação USPTO

Active USPTO registration

Tipo de processo

Pedido e registro

Eventos registrados

14

Atualização mais recente

21/05/2024

Classificação

Registrada

Tipo de marca

Mista

Classes Nice

35, 42, 45

Data de depósito

01/05/2023

Data de registro

21/05/2024

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

21/05/2024

Última transação

21/05/2024

Escritório responsável

United States Patent and Trademark Office

Código da situação

700

Cadastro oficial

Principal Register

Primeiro uso

31/10/2022

Primeiro uso no comércio

31/10/2022

Código do desenho

3

Tipo de titular

16

Localização do titular

Lake Mary, FL, US

Examinador

PHILLIPS, WENDELL

Unidade examinadora

M10

Localização atual

FILE REPOSITORY (FRANCONIA)

Descrição da marca

The mark consists of a stylized "A" comprised of four curved triangles.

Titulares e representantes

Titulares

Clinical Research Holdings, LLC

Representantes

Mark A. Wright McLane Middleton, P.A.

Classificação técnica

Classes Nice

Classe 35Classe 42Classe 45

Códigos Vienna

Sem códigos Vienna disponíveis.

Produtos e serviços

Classe 35

Business consulting and management in the field of clinical trials in all phases as it relates to pre-study document collection and reviewsite selectionvisits and auditssite complianceproject tracking and monitoring reportsnegotiation and administration of investigator grants and clinical trial budgets and contractsfinancial and management accountingdistributioncoordination and tracking of clinical trial products and materialsregulatory document processinglaboratory selection and coordination; Business consulting and management in the field of clinical trials in all phases as it relates to managing site and study-specific subject recruitment strategies and programs in the nature of contingency strategies and solutions to address specific project challenges; Business consulting and management in the field of clinical trials in all phases as it relates to managing the development of all study related documents and materials in the nature of study protocolscontractsbudgetsamendmentspaper and electronic case report formsinformed consent formssafety narrativespresentation posterstraining manuals; Business consulting and management in the field of clinical trials in all phases as it relates to managing all aspects of studydrug reconciliationinventory and distribution reports; Business management for all aspects of clinical trials in all phases as it relates to managing investigatorscoordinatorsmonitorstechniciansparticipants for compliance with clinical protocols and regulations; Business consulting and management in the field of clinical trials in all phases as it relates to management and compilation of computerized databases in the field of clinical trials for business purposes; Business consulting and management in the field of clinical trials in all phases as it relates to ethical reviewssubmitting clinical trial protocols to institutional review boards and independent ethics committees on behalf of medicalbiopharmaceutical and biotechnology companies to assist them with clinical trials; Statistical analysis and reporting services for business purposes in the field of clinical trials; Business project management in the field of clinical trials in all phases as it relates to organizing and conducting business meetings of clinical trial investigators; Business managementmanaging randomization logisticsin the pharmaceutical and biotechnological field for business purposes; Development and implementation of personnel recruitment and retention programs for investigatorscoordinatorsmonitorstechnicians and participants for use in clinical trials; Business consulting and management in the field of clinical trials in all phases as it relates to the administration of protocols involving volunteer research patients and the recruiting of such volunteer research patients; Providing data management services in the medicalpharmaceutical and biotechnological field for business purposes

Classe 42

Medical and scientific research consulting services for others in the field of designplanningimplementation of clinical trials in all phases; providing quality assurance services in the pharmaceutical and biotechnological industries

Classe 45

Regulatory affairsreviewing standards and practices to assure compliance with clinical trial laws and regulations; 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

Publicações

Histórico de despachos e eventos da marca no USPTO.

14 publicações encontradas

NRCC

NOTICE OF REGISTRATION CONFIRMATION EMAILED

21/05/2024

R.PR

REGISTERED-PRINCIPAL REGISTER

21/05/2024

NPUB

OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED

05/03/2024

PUBO

PUBLISHED FOR OPPOSITION

05/03/2024

NONP

NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED

14/02/2024

NPUB

OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED

14/02/2024

TCCA

TEAS CHANGE OF CORRESPONDENCE RECEIVED

29/01/2024

ARAA

ATTORNEY/DOM.REP.REVOKED AND/OR APPOINTED

29/01/2024

REAP

TEAS REVOKE/APP/CHANGE ADDR OF ATTY/DOM REP RECEIVED

29/01/2024

CNSA

APPROVED FOR PUB - PRINCIPAL REGISTER

26/01/2024

DOCK

ASSIGNED TO EXAMINER

26/01/2024

MDSM

NOTICE OF DESIGN SEARCH CODE E-MAILED

31/05/2023

NWOS

NEW APPLICATION OFFICE SUPPLIED DATA ENTERED

30/05/2023

NWAP

NEW APPLICATION ENTERED

04/05/2023

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