NRCC
NOTICE OF REGISTRATION CONFIRMATION EMAILED
19/07/2022
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Dado oficial do USPTO
USDM
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Active USPTO registrationTipo: VerbalEscritório: US
Snapshot rápido
USDM
ST13
US500000090026935Classe
35, 41, 42, 45
Pedido
90026935
Registro
6791916
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
28
Atualização mais recente
01/07/2023
Classificação
Registrada
Tipo de marca
Verbal
Classes Nice
35, 41, 42, 45
Data de depósito
29/06/2020
Data de registro
19/07/2022
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
19/07/2022
Última transação
01/07/2023
Escritório responsável
United States Patent and Trademark Office
Código da situação
700
Cadastro oficial
Principal Register
Fundamento do pedido
Intent to use
Primeiro uso
05/11/2013
Primeiro uso no comércio
05/11/2013
Código do desenho
4
Tipo de titular
16
Localização do titular
Santa Barbara, CA, US
Examinador
BEVERLY, JOSETTE
Unidade examinadora
M60
Localização atual
PUBLICATION AND ISSUE SECTION
Titulares e representantes
Titulares
US Data Management, LLC
Representantes
Darren B. Cohen REED SMITH LLP
Classificação técnica
Classes Nice
Classe 35Classe 41Classe 42Classe 45
Códigos Vienna
Sem códigos Vienna disponíveis.
Produtos e serviços
Classe 35
Business advisorydevelopmentstrategic planning services provided to companies for business purposes in the life sciences industries; Business consultation services in the field of GxP (Good Practice) compliance; Business consulting services on processes and workflows related to content creationlocalization and publishing strategy including Translation Memory and Terminology ManagementQuality ManagementLife Sciences Regulatory Compliance and Risk Management; Business consulting and management in the field of clinical trialsclinical data and regulatory submission management on behalf of medicalbiopharmaceutical and biotechnology companies to assist them with clinical researchclinical trials and applications for drug approval; Regulatory submission managementassisting others in preparing and filing applications for new medical devicesmedical technologiesmedicationsbiopharmaceuticalsbiotechnology with governmental regulatory bodies around the world; Regulatory submission managementproviding simultaneous multiple country submissions of applications for the registration and approval of medical devicesmedical technologiesmedicationsbiopharmaceuticalsbiotechnology; providing information online regarding regulatory submission management; Business management consultingstrategic planning and business advisory services provided to medicalmedical technologybiopharmaceuticalbiotechnology companiesgovernment agencieseducational and research institutionslaw firmsinvestment firms in the fields of biologicspharmaceuticals and medical devices; Providing consulting services in the field of regulatory submission management to medical companies to assist them with applications for drug and medical device approval; Regulatory submission managementassisting others in preparing and filing applications for new drugs and medical devices with governmental regulatory bodies; Business consulting services in the field of biologicspharmaceuticalsprescription drugs and medical devices; Business consulting and management for companies in the life sciences fields pertaining to business operations including standard operating proceduresaudits and assessments; Business consulting and for companies in the life sciences fields related to supply chain managementincludinginternet of medical things (IoMT)connected service and quality managementproduct lifecycle managementproduct master managemententerprise resource planning; Providing IT staffing services for companies in the life sciences fields and employment consultation pertaining to staffing augmentation services and onsite and remote on-demand compliance staff augmentation; Business consulting and management for companies in the life sciences fields pertaining to business operations including information and data compiling and analyzing relating to business management; consulting services in the field of medical device product approval for commercial purposes
Classe 41
Providing educational programs in the life science fields using on-line activitiesnon-downloadable webinars and blogsworkshopsprintable materials distributed therewith featuring Regulatory issues and developmentsGxP (Good Practice) ComplianceRisk ManagementDesign ControlQMS (Quality Management Solutions)CSV (Computer System Validation)SOP (Standard Operating Procedures)Data IntegrityUDI (Unique Device Identification)Regulatory readinessother related practice areas in the life sciences fields
Classe 42
Consulting services in the fields of biotechnologypharmaceutical research and development and genetic science; biotechnology research consulting services; pharmaceutical research and product development for use in manufacturing; information technology consultation services; computer aided design services; Consulting services for others in the field of designing pre-clinical and clinical studies and trials for others; product research and development for others in the fields of biologicspharmaceuticalsprescription drugs and medical devices; quality management servicesquality evaluation and analysisquality assurance and quality control in the field of biologicspharmaceuticalsprescription drugs and medical devices; scientific consulting and research services relating to the field of pharmaceuticalsmedical deviceslife sciencesbiologymedicine; design and development and technical verification consulting services in the fields of biotechnology and pharmaceutical researchscientific and technological servicesscientific researchanalysistestingrelated scientific studies in the field of chemistry and molecular biologybiologics and protein detectioncharacterizationanalysis and testing; Computer consulting services in the field of cloud computing in the field of life science; Technical and scientific research consulting and computer project management for companies in the life sciences fields pertaining to cloud-based data migration; Technical and scientific consulting and management for companies in the life sciences fields pertaining to technical verification and validation laboratory equipment and instrumentation; Technical and scientific consulting and management for companies in the life sciences fields for digital purposesincluding digital compression of computer data; Technical and scientific consulting and management for companies in the life sciences fields for cloud computing purposesincluding GxP (Good Practice) cloud seeding services
Classe 45
Regulatory compliance consulting services in the life sciences fieldsreviewing standards and practices to assist clients with compliance with governmental lawsregulations and rules pertaining to medical devicesmedical technologiesmedicationsbiopharmaceuticalsbiotechnology; providing technical regulatory affair consulting services directed to medicalmedical technologybiopharmaceuticalbiotechnology companies in order to assure compliance with food and drug administration's laws and regulations; provision of information online pertaining to regulatory compliance in the fields of medical devicesmedical technologiesmedicationsbiopharmaceuticalsbiotechnology; and regulatory compliance consulting in the fields of biologicspharmaceuticalsprescription drugs and medical device
Publicações
Histórico de despachos e eventos da marca no USPTO.
28 publicações encontradas
R.PR
REGISTERED-PRINCIPAL REGISTER
19/07/2022
NPUB
OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED
03/05/2022
PUBO
PUBLISHED FOR OPPOSITION
03/05/2022
NONP
NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED
13/04/2022
AAUA
NOTICE OF ACCEPTANCE OF AMENDMENT TO ALLEGE USE E-MAILED
01/04/2022
CNSA
APPROVED FOR PUB - PRINCIPAL REGISTER
31/03/2022
IUAA
USE AMENDMENT ACCEPTED
31/03/2022
AUPC
AMENDMENT TO USE PROCESSING COMPLETE
30/03/2022
IUAF
USE AMENDMENT FILED
30/03/2022
EAAU
TEAS AMENDMENT OF USE RECEIVED
29/03/2022
TEME
TEAS/EMAIL CORRESPONDENCE ENTERED
28/03/2022
CRFA
CORRESPONDENCE RECEIVED IN LAW OFFICE
27/03/2022
ERSI
TEAS RESPONSE TO SUSPENSION INQUIRY RECEIVED
27/03/2022
RCSC
REPORT COMPLETED SUSPENSION CHECK CASE STILL SUSPENDED
20/11/2021
RCCK
SUSPENSION CHECKED - TO ATTORNEY FOR ACTION
08/11/2021
GNS3
NOTIFICATION OF LETTER OF SUSPENSION E-MAILED
05/05/2021
GNSL
LETTER OF SUSPENSION E-MAILED
05/05/2021
CNSL
SUSPENSION LETTER WRITTEN
05/05/2021
TEME
TEAS/EMAIL CORRESPONDENCE ENTERED
16/04/2021
CRFA
CORRESPONDENCE RECEIVED IN LAW OFFICE
15/04/2021
TROA
TEAS RESPONSE TO OFFICE ACTION RECEIVED
15/04/2021
GNRN
NOTIFICATION OF NON-FINAL ACTION E-MAILED
15/10/2020
GNRT
NON-FINAL ACTION E-MAILED
15/10/2020
CNRT
NON-FINAL ACTION WRITTEN
15/10/2020
DOCK
ASSIGNED TO EXAMINER
30/09/2020
NWOS
NEW APPLICATION OFFICE SUPPLIED DATA ENTERED
28/07/2020
NWAP
NEW APPLICATION ENTERED
02/07/2020
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