NRCC
NOTICE OF REGISTRATION CONFIRMATION EMAILED
02/07/2024
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Dado oficial do USPTO
MEDPRO SYSTEMS
Sabia que essa marca já está registrada no Estados Unidos?
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Active USPTO registrationTipo: MistaEscritório: US
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
16
Atualização mais recente
02/07/2024
Classificação
Registrada
Tipo de marca
Mista
Classes Nice
35, 41, 42, 45
Data de depósito
19/06/2023
Data de registro
02/07/2024
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
02/07/2024
Última transação
02/07/2024
Escritório responsável
United States Patent and Trademark Office
Código da situação
700
Cadastro oficial
Principal Register
Primeiro uso
01/04/2021
Primeiro uso no comércio
01/04/2021
Código do desenho
3
Tipo de titular
16
Localização do titular
Mt. Arlington, NJ
Examinador
BLOHM, LINDA
Localização atual
FILE REPOSITORY (FRANCONIA)
Descrição da marca
The mark consists of a rectangle consisting of two interlocking puzzle pieces. The puzzle piece on the left is gray and contains the word "MEDPRO" in white, and the puzzle piece on the right is navy blue and contains the word "SYSTEMS" in white.
Titulares e representantes
Titulares
MedPro Systems LLC
Representantes
Christine Amara SHERMAN ATLAS SYLVESTER & STAMELMAN LLP
Classificação técnica
Classes Nice
Classe 35Classe 41Classe 42Classe 45
Códigos Vienna
Sem códigos Vienna disponíveis.
Produtos e serviços
Classe 35
Business consulting services for life sciencespharmaceuticalsbiotechnology and medical device companies in the nature of regulatory compliance program development and enhancement and transparency program supportreviewing program status and performing gap analysesdrafting programs plansprogram implementation supportdevelopment and improvement of policiesstandard operating procedures and codes of conduct; business consulting services in the nature of monitoring of pharmaceutical and medical device manufacturer interactions with healthcare professionalshealthcare organizationspatientsother customers; business consulting services in the nature of auditing of pharmaceutical and medical device manufacturer interactions with and payments to healthcare professionalshealthcare organizationspatientsother customers; business consulting services in the nature of business investigation support for internally and externally raised complaints made against a pharmaceutical or medical device manufacturer related to potential violations of their company policy or codeindustry codelaw or regulation; transparency reporting regulatory submission managementassisting others in preparing and filing regulatory submissions in the field of transparency reporting for pharmaceuticalbiotechnology and medical device companies; business consulting servicestracking and monitoring regulatory requirements for others in the field of life sciencespharmaceuticalsbiotechnologymedical devices for regulatory compliance; business consulting servicescompliance program gap analysis for life sciencespharmaceuticalbiotechnologymedical device companies
Classe 41
Consulting services in the nature of conducting trainings for life sciencespharmaceuticalsbiotechnologymedical device companies personnel and partners on pharmaceutical and medical device compliance program requirementsfraud and corruption laws and regulationsindustry codes and best practices; consulting servicesdeveloping and providing trainings for life sciencespharmaceuticalbiotechnologymedical device companies in the field of corporate compliance and transparency programs
Classe 42
Software as a service (SaaS) services featuring software for use to assist in tracking and reporting healthcare practitioner and healthcare organization interactions and complying with internationalfederalstate and local spend and transparency laws and regulations; software as a service (SaaS) services featuring software to assist pharmaceuticalbiotechnology and medical device companies in managingvalidating and enriching healthcare organization and healthcare practitioner data attributes in connection with regulatory compliancesales and marketing efforts
Classe 45
Regulatory compliance consulting in the field of life sciencespharmaceuticalsbiotechnologymedical devices; consulting services to assist life sciencespharmaceuticalbiotechnology and medical device companies in the fields of regulatory compliancecompliance in the areas of aggregate spend disclosure reportingthe Prescription Drug Marketing Actthe Drug Supply Chain Security ActCondition of Participation for Outpatient ServicesStark Law and Ohio Terminal Distributor of Dangerous Drugs requirements; regulatory compliance audits for life sciencespharmaceuticalbiotechnology and medical device companies to assist with regulatory compliance; consulting services in the field of life sciencespharmaceuticalbiotechnology and medical device corporate compliance program and transparency program developmentimplementation and support; providing online searchable databases and information concerning historicalcurrent and pending lawsregulationsguidance documents governing the life sciences industry; regulatory compliance consulting services in the field of aggregate spend disclosure reporting; regulatory and compliance information for pharmaceuticalbiotechnology and medical device companiesfor entities involved in the drug and device supply chainregarding transparency and aggregate spendmarketingadditional compliance requirements; regulatory compliance consultingreviewingdevelopingtraining on and assisting with the implementation and monitoring of standardspracticesprocedures and policies to support regulatory compliance for companies in the fields of life sciencespharmaceuticalsbiotechnologymedical devices
Publicações
Histórico de despachos e eventos da marca no USPTO.
16 publicações encontradas
R.PR
REGISTERED-PRINCIPAL REGISTER
02/07/2024
NPUB
OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED
16/04/2024
PUBO
PUBLISHED FOR OPPOSITION
16/04/2024
NONP
NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED
27/03/2024
CNSA
APPROVED FOR PUB - PRINCIPAL REGISTER
11/03/2024
TEME
TEAS/EMAIL CORRESPONDENCE ENTERED
05/03/2024
CRFA
CORRESPONDENCE RECEIVED IN LAW OFFICE
05/03/2024
TROA
TEAS RESPONSE TO OFFICE ACTION RECEIVED
05/03/2024
GNRN
NOTIFICATION OF NON-FINAL ACTION E-MAILED
01/03/2024
GNRT
NON-FINAL ACTION E-MAILED
01/03/2024
CNRT
NON-FINAL ACTION WRITTEN
01/03/2024
DOCK
ASSIGNED TO EXAMINER
26/02/2024
MDSC
NOTICE OF DESIGN SEARCH CODE E-MAILED
22/07/2023
NWOS
NEW APPLICATION OFFICE SUPPLIED DATA ENTERED
21/07/2023
NWAP
NEW APPLICATION ENTERED
22/06/2023
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