IPAS770
Concessão de registro em designação
RPI 2795
30/07/2024
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Dado oficial do INPI
CAIDYA
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Registro de marca em vigor (Madri)Tipo: VerbalEscritório: Brasil
Snapshot rápido
CAIDYA
ST13
BR500000501739797Classe
9, 10, 16, 35, 37, 38, 39, 41, 42, 44, 45
Pedido
501739797
Registro
501739797
Andamento no INPI
- Depósito02/02/23
- Publicação23/01/24
- Exame
- Deferimento21/05/24
- Concessão30/07/24
- Vigente02/02/33
Registro concedido em 30/07/2024 e em vigor até 02/02/2033, quando precisa ser renovado.
Proteção válida até:02/02/2033
Última movimentação publicada pelo INPI: 30/07/2024. Atualizamos a cada nova RPI, publicada semanalmente.
Diagnóstico de risco e oportunidade
Leitura executiva para decisão de naming, protocolo e monitoramento.
Situação INPI
Registro de marca em vigor (Madri)
Tipo de processo
Pedido e registro
Eventos registrados
3
Atualização mais recente
30/07/2024
Tipo de marca
Verbal
Classes Nice
9, 10, 16, 35, 37, 38, 39, 41, 42, 44, 45
Data de depósito
02/02/2023
Data de registro
30/07/2024
Data de expiração
02/02/2033
Dados completos do processo
Campos estruturados da autoridade responsável e do histórico oficial.
Natureza
Madri
Produto/Serviço
Escritório responsável
Brasil
Tipo de titular
NÃO RESIDENTE
Localização do titular
US
Titulares e representantes
Titulares
Clinipace, Inc.
Representantes
Sem dados de representantes.
Classificação técnica
Classes Nice
Classe 9Classe 10Classe 16Classe 35Classe 37Classe 38Classe 39Classe 41Classe 42Classe 44Classe 45
Códigos Vienna
Sem códigos Vienna disponíveis.
Produtos e serviços
Classe 9
Computer software, namely, computer programs, computer program systems and program libraries, databases recorded on a data carrier in the field of pharmaceutical research and development
Classe 10
Medical apparatus, namely health monitoring equipment for clinical trials
Classe 16
Printed users manuals
Classe 35
Business consulting and management in the field of clinical trials, namely, clinical data and regulatory submission management on behalf of pharmaceutical, medical, healthcare, and life sciences companies to assist them with clinical research, clinical trials and applications for drug, biologic and device approvalbusiness analysis, namely providing independent review of clinical trials for business purposescontract research organization (CRO) services, namely, business management in the field of clinical trials, namely, clinical data management
Classe 37
Real estate site selection, namely, construction consultation in the course of building construction
Classe 38
Providing user access to a global computer network in connection with clinical trials and drug developmentprovision of access to a computer network in connection with clinical trials and drug development
Classe 39
Clinical trial logistical services such as delivering clinical trial kits to sites, delivering wearables to patients and/or site locations
Classe 41
Contract research organization (CRO) services, namely, custom writing for others for non-advertising purposes in the nature of medical writing of clinical study protocols and reportsconsultation in the field of publishing and issuing scientific papers in relation to conducting clinical trials, regulatory affairs, drug development, manufacturing compliance and validation, advanced technology, clinical benchmarking and clinical performance improvement in the field of international health and in the pharmaceutical, biotechnology, and medical device industries
Classe 42
Contract research organization (CRO) services, namely, monitoring of clinical trials for drugs, biologics and devices of pharmaceutical, medical, healthcare, and life sciences companies for quality control purposes, and clinical trial project management in the nature of design and implementation of clinical trials and quality assurance for all major therapeutic areas, in particular gastroenterology, nephrology, urology, and oncologyconsulting services in the field of conducting clinical trials in the pharmaceutical industry, the biotechnology industry and the medical device and diagnostics industriesproviding quality assurance services in the field of regulatory submissions to the FDA by life sciences companies to ensure validity and accuracyproduct development for others, namely, providing implementation services relating to the development and validation of drugs, biologics and medical devicessoftware as a service (SaaS) services featuring software for accessing, collecting, managing, tracking, analyzing, and reporting data and information on clinical trialsproviding quality assurance services in the field of regulatory submissions to regulatory authorities and government agencies by life sciences companies to ensure validity and accuracy of clinical trials
Classe 44
Medical and pharmaceutical consultation
Classe 45
Legal assistance services, namely providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of researchregulatory compliance consulting in the pharmaceutical, medical, healthcare, and life sciences fields
Publicações
Histórico de despachos e eventos da marca no INPI.
3 publicações encontradas
IPAS768
Deferimento de designação
RPI 2785
21/05/2024
IPAS756
Publicação de pedido de registro para oposição (exame formal de designação concluído)
RPI 2768
23/01/2024
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