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Dado oficial do USPTO

CAIDYA

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: VerbalEscritório: US

Snapshot rápido

CAIDYA

ST13

US500000097533860

Classe

35, 42, 45

Pedido

97533860

Registro

7517006

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

26

Atualização mais recente

24/09/2024

Classificação

Registrada

Tipo de marca

Verbal

Classes Nice

35, 42, 45

Data de depósito

03/08/2022

Data de registro

24/09/2024

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

24/09/2024

Última transação

24/09/2024

Escritório responsável

United States Patent and Trademark Office

Código da situação

700

Cadastro oficial

Principal Register

Fundamento do pedido

Intent to use

Primeiro uso

03/10/2022

Primeiro uso no comércio

03/10/2022

Código do desenho

4

Tipo de titular

03

Localização do titular

Morrisville, NC

Examinador

GANDARA, KEYLA

Unidade examinadora

N30

Localização atual

PUBLICATION AND ISSUE SECTION

Titulares e representantes

Titulares

Clinipace, Inc.

Representantes

Margarita Wallach, Esq. MCCARTER & ENGLISH, LLP

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 trialsclinical data and regulatory submission management on behalf of pharmaceuticalmedicalhealthcarelife sciences companies to assist them with clinical researchclinical trials and applications for drugbiologic and device approval; providing independent review of clinical trials for business purposes; Contract research organization (CRO) servicesbusiness management in the field of clinical trialsclinical data management

Classe 42

Contract research organization (CRO) servicesmonitoring of clinical trials for drugsbiologics and devices of pharmaceuticalmedicalhealthcarelife sciences companies for quality control purposesclinical trial project management in the nature of design and implementation of clinical trials and quality assurance for all major therapeutic areasin particular gastroenterologynephrologyurologyoncology; consulting services in the field of scientific research in the nature of conducting clinical trials in the pharmaceutical industrythe biotechnology industry and the medical device and diagnostics industries; providing quality assurance services in the field of regulatory submissions to the FDA by life sciences companies to ensure validity and accuracy; product development for othersproviding implementation services relating to the development and validation of drugsbiologics and medical devices; Software as a service (SaaS) services featuring software for accessingcollectingmanagingtrackinganalyzingreporting data and information on clinical trials; Contract research organization (CRO) servicescustom technical writing for others for non-advertising purposes in the nature of medical writing of clinical study protocols and reports; Contract research organization (CRO) servicescustom writing for others for non-advertising purposes in the nature of medical writing of clinical study protocols and reports for submission to regulatory authorities

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 pharmaceuticalmedicalhealthcarelife sciences fields

Publicações

Histórico de despachos e eventos da marca no USPTO.

26 publicações encontradas

NRCC

NOTICE OF REGISTRATION CONFIRMATION EMAILED

24/09/2024

R.PR

REGISTERED-PRINCIPAL REGISTER

24/09/2024

SUNA

NOTICE OF ACCEPTANCE OF STATEMENT OF USE E-MAILED

17/08/2024

CNPR

ALLOWED PRINCIPAL REGISTER - SOU ACCEPTED

17/08/2024

SUPC

STATEMENT OF USE PROCESSING COMPLETE

01/08/2024

AITU

CASE ASSIGNED TO INTENT TO USE PARALEGAL

01/08/2024

IUAF

USE AMENDMENT FILED

12/06/2024

EISU

TEAS STATEMENT OF USE RECEIVED

12/06/2024

NOAM

NOA E-MAILED - SOU REQUIRED FROM APPLICANT

12/12/2023

NPUB

OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED

17/10/2023

PUBO

PUBLISHED FOR OPPOSITION

17/10/2023

NONP

NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED

27/09/2023

CNSA

APPROVED FOR PUB - PRINCIPAL REGISTER

07/09/2023

XAEC

EXAMINER'S AMENDMENT ENTERED

07/09/2023

GNEN

NOTIFICATION OF EXAMINERS AMENDMENT E-MAILED

07/09/2023

GNEA

EXAMINERS AMENDMENT E-MAILED

07/09/2023

CNEA

EXAMINERS AMENDMENT -WRITTEN

07/09/2023

TEME

TEAS/EMAIL CORRESPONDENCE ENTERED

01/09/2023

CRFA

CORRESPONDENCE RECEIVED IN LAW OFFICE

01/09/2023

TROA

TEAS RESPONSE TO OFFICE ACTION RECEIVED

01/09/2023

GNRN

NOTIFICATION OF NON-FINAL ACTION E-MAILED

01/06/2023

GNRT

NON-FINAL ACTION E-MAILED

01/06/2023

CNRT

NON-FINAL ACTION WRITTEN

01/06/2023

DOCK

ASSIGNED TO EXAMINER

19/05/2023

NWOS

NEW APPLICATION OFFICE SUPPLIED DATA ENTERED

25/08/2022

NWAP

NEW APPLICATION ENTERED

06/08/2022

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