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Dado oficial do USPTO

PRC CLINICAL

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

PRC CLINICAL

ST13

US500000086839995

Classe

35, 36, 41, 42, 45

Pedido

86839995

Registro

5107883

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

21

Atualização mais recente

28/12/2025

Classificação

Registrada

Tipo de marca

Verbal

Classes Nice

35, 36, 41, 42, 45

Data de depósito

04/12/2015

Data de registro

27/12/2016

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

28/06/2023

Última transação

28/12/2025

Escritório responsável

United States Patent and Trademark Office

Código da situação

705

Cadastro oficial

Principal Register

Primeiro uso

2010-11-00

Primeiro uso no comércio

2010-11-00

Código do desenho

4

Tipo de titular

03

Localização do titular

San Mateo, CA

Examinador

PARKER,JUSTINE D

Unidade examinadora

L10

Titulares e representantes

Titulares

P. C. (pessoa física)
P. C. (pessoa física)

Representantes

Michael J. Leonard FOX ROTHSCHILD, LLP

Classificação técnica

Classes Nice

Classe 35Classe 36Classe 41Classe 42Classe 45

Códigos Vienna

Sem códigos Vienna disponíveis.

Produtos e serviços

Classe 35

Business process outsourcing services for others in the fields of pharmacy and healthcare; Consumer research services in the field of drug safetycollectinganalyzingprocessing data related to adverse events and product quality complaintsaggregate reporting of adverse events and product quality complaintsproduct life cycle case handling related to adverse events and product quality complaints; Business management services in the field of clinical trialscompilation and management of regulatory submission data on behalf of medicalbiopharmaceutical and biotechnology companies to assist them with clinical researchclinical trials and applications for drug approval; Business consulting services in the field of medical clinical trials management; Data collection services for business purposes in the nature of extractingsummarizinganalyzing and validating information from medical records in the field of clinical trials management; Business data compilation and tracking services for othersinteractive tracking of clinical trial subject enrollmentstatus and adverse/side effects of treatment and medication; Compiling and analyzing statisticsdata and other sources of information for business purposes

Classe 36

payment processing services in the field of FDA clinical trial payments

Classe 41

Education servicesproviding of classesseminarsworkshopsworking groups and panel discussions the field of clinical trials and medical research; providing clinical research education classes to healthcare professionals

Classe 42

Consulting services for others in the field of designplanningimplementation project management of clinical trials; Providing medical and scientific research information in the fields of pharmaceuticalsdrug safetyclinical researchclinical testing and clinical trials; medical research and scientific research and scientific consulting servicesdesigning and conducting scientific research drug safety and dosage assessment and drug compatibility studies; Providing quality assurance services in the field of clinical trials; Testinganalysisevaluation of clinical trials of others to assure compliance with industry standards; Providing temporary use of non-downloadable software for use in accessingmanaginganalyzing data in the fields of clinical trials and drug safety; Providing informationadvice and consulting in the field of drug safety testing

Classe 45

Regulatory compliance consulting in the field of clinical trials

Publicações

Histórico de despachos e eventos da marca no USPTO.

21 publicações encontradas

REM2

COURTESY REMINDER - SEC. 8 (10-YR)/SEC. 9 E-MAILED

27/12/2025

NA85

NOTICE OF ACCEPTANCE OF SEC. 8 & 15 - E-MAILED

28/06/2023

C15P

REGISTERED - PARTIAL SEC. 8 (6-YR) ACCEPTED & SEC. 15 ACK.

28/06/2023

APRE

CASE ASSIGNED TO POST REGISTRATION PARALEGAL

28/06/2023

E815

TEAS SECTION 8 & 15 RECEIVED

05/01/2023

REM1

COURTESY REMINDER - SEC. 8 (6-YR) E-MAILED

27/12/2021

R.PR

REGISTERED-PRINCIPAL REGISTER

27/12/2016

NPUB

OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED

11/10/2016

PUBO

PUBLISHED FOR OPPOSITION

11/10/2016

NONP

NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED

21/09/2016

CNSA

APPROVED FOR PUB - PRINCIPAL REGISTER

03/09/2016

TEME

TEAS/EMAIL CORRESPONDENCE ENTERED

30/08/2016

CRFA

CORRESPONDENCE RECEIVED IN LAW OFFICE

29/08/2016

TROA

TEAS RESPONSE TO OFFICE ACTION RECEIVED

29/08/2016

GNRN

NOTIFICATION OF NON-FINAL ACTION E-MAILED

15/03/2016

GNRT

NON-FINAL ACTION E-MAILED

15/03/2016

CNRT

NON-FINAL ACTION WRITTEN

15/03/2016

DOCK

ASSIGNED TO EXAMINER

09/03/2016

MPMK

NOTICE OF PSEUDO MARK E-MAILED

10/12/2015

NWOS

NEW APPLICATION OFFICE SUPPLIED DATA ENTERED

09/12/2015

NWAP

NEW APPLICATION ENTERED

08/12/2015

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