Drawing for REQUALITE

USPTO serial 79374035

REQUALITE

Reviewed by CopyMark Law Group

Reg. 7561478Status 700Registered
Filing date
Status date
Registration date
Nov 12, 2024
Examiner
OSGOOD, KRYSTINA E
Law office
FILE REPOSITORY (FRANCONIA)

What this means

Status 700 means the trademark is registered and active on the Principal Register. You have nationwide rights for the listed goods and services and may use ®. Section 8 maintenance is due between years five and six. Calendar Section 8 between years five and six, and consider trademark monitoring.

Status 700: Status 700 means the trademark is registered and active on the Principal Register. You have nationwide rights for the listed goods and services and may use ®. Section 8 maintenance is due between years five and six.

Need help with REQUALITE?

If you own this trademark, we can monitor new filings and help with USPTO deadlines. If you do not, we can file a new U.S. application.

Current trademark owner
Monitor this mark, or talk with CopyMark about this registration.
Not the owner?
File a new U.S. trademark application, or speak with our attorneys.

Owner

Attorney of record

The USPTO lists this attorney as the applicant's representative for correspondence on this application.

Thilo C. Agthe

Thilo C. Agthe Wuersch & Gering LLP100 Wall Street, 10th FloorNew York, NY 10005United States

Goods and services

ClassDescriptionStatusFirst use
035Business consultancy services relating to the supply of quality management systems; market reporting services, namely, preparation of marketing reports; business advisory services relating to the management of businesses; business advisory services for business management; advice relating to the organization and management of business; business management and organization consultancy; business consultancy relating to data processing; business consultancy relating to business document management; business planning consultancy; professional business consultancy; business process management and consulting; assistance and advice regarding business organization and management; business research; conducting online business management research surveys; business appraisals; evaluations relating to commercial matters; writing being preparation of business project reports; writing being preparation of business project studies reports; writing being preparation of business reports; administering of professional certifications, namely, business administration of regulatory and certification affairs of medical device manufacturers; maintaining a registry of certified medical technical professionals; business advisory and consultancy services relating to obtaining and maintaining commercial product certifications; business advisory and consultancy services relating to obtaining and maintaining commercial product certifications for medical devices; business administrative support and data processing services; employee administration support services for employees with regard to business matters; statistical analysis and reporting for business purposes; compilation of scientific information into computer databasesACTIVE—
041Education services relating to quality services, namely, providing classes in the field of business quality services; consultancy services relating to the business training of employees; consultation services relating to the publication of written texts; consultation services relating to the publication of magazines; advice relating to medical training; advisory services relating to book publishing; consultancy and information services relating to arranging, conducting and organization of symposiums; consultancy relating to arranging, conducting and organization of conferences; providing information relating to education services in the field of arranging conducting and organization of symposiums; consultancy relating to arranging, conducting and organization of congresses; providing information relating to education services in the field of arranging conducting and organization of congresses; IT training; information on education; advisory consultation services relating to education; training in business management; education services relating to medicine, namely, training and teaching in the field of medical device and in vitro diagnostic (IVD) medical device regulations; vocational training services in the field of medical device and in vitro diagnostic (IVD) medical device regulations; career coaching services; legal education services, namely, providing continue professional education seminars in the legal field; publication of instructional literature books and magazines; reference libraries of literature and documentary records; publishing of written text, news syndication reporting, and writing of articles for journals other than for advertising or publicity; creation of educational content for podcasts, namely, creating educational podcast content in the field of medical device and in vitro diagnostic (IVD) medical device regulations for non-advertising purposes; writing of articles for journals other than for advertising or publicity purposes; written text editing services other than publicity texts; speech writing for non-advertising purposes and publication of texts, other than publicity texts; writing of texts, namely, writing of articles for journals other than for advertising or publicity; writing services for blogs, namely, writing of articles for journals other than for advertising or publicity; educational services, namely, conducting educational support programs for healthcare professionals; providing computer-delivered educational testing and assessmentsACTIVE—
042Scientific and technological services, namely, scientific research; consultancy in the field of scientific research, namely, scientific research consulting in the field of medical devices; consultancy services relating to quality control for others; quality assurance consultancy in the field of medical devices; quality control being quality control for others; providing quality assurance services in the field of medical devices; conducting of quality control tests, namely, product quality testing; quality control testing, namely, product quality evaluation; quality checking, namely, quality control of services; quality audits, namely, quality control for others; quality checking and testing, namely, quality testing of quality management systems necessary to obtain medical device approvals and registrations; process monitoring for quality assurance, namely, monitoring services for tracking quality management systems necessary to obtain medical device approvals and registrations; testing, authentication and quality control, namely, quality control of internal quality management systems necessary to obtain medical device approvals and registrations; quality control for others and user authentication services using technology for e-commerce transactions; quality control of services; inspection of pharmaceuticals; quality testing of products for certification purposes; certification, namely, testing analysis and evaluation of the goods of others to determine conformity with certification standards; testing services of others to determine conformity with certification standards; consultancy relating to biotechnology; consultancy relating to research in the field of pharmacogenetics; consultancy relating to scientific research and development in the field of therapeutics; consultancy pertaining to pharmacology; advisory services relating to material testing in the field of biochemistry; advisory services relating to scientific research; advisory services relating to product testing; consultancy in the field of pharmaceutical research; advisory services relating to gene therapy research; technical consulting in the field of environmental engineering; technological consultancy in the field of medical devices; advisory services relating to the certification and registration of medical devices; advisory services relating to scientific instruments, namely, consultation relating to medical device products development; professional consultancy relating to the science of ergonomics, namely, designing workplace facilities and equipment to optimize efficiency and safety; design and development of medical diagnostic apparatus; scientific research and development in the field of diagnostic preparations; expert reporting services relating to technology, namely, reporting of online website performance to determine technological effectiveness of the websites for non-business purposes in connection with the processing of clinical-medical data and data on biocompatibility; providing scientific research information and results from an online searchable database in the field of medical devices; technical writing; technical writing for others; testing, analysis and evaluation of the goods of others to determine conformity with certification standards for the purpose of certification; testing, analysis and evaluation of the services of others for the purpose of certification, namely, testing, analysis and evaluation of the services of others to determine conformity with certification standards; testing services for the certification of quality or standards, namely, testing of the services of others to determine conformity with certification standards; testing of apparatus of others in the field of medical devices to determine conformity with certification standards for certification purposes; information technology support services, namely, troubleshooting of computer software problems and computer operating system problems; provision of technical support, namely, troubleshooting of computer software problems in the operation of computing networks; providing information on clinical studies via an interactive website; providing medical and scientific research information in the field of pharmaceuticals and clinical trials; clinical research in the field of in vitro diagnostic (IVD) medical devices; biological research, medical research; analysis and evaluation of product development of the goods of others to assure compliance with industry standards; analysis and evaluation of product designs of the goods of others to assure compliance with industry standards; conducting early evaluations in the field of new pharmaceuticals; pharmaceutical product evaluation; product quality evaluationACTIVE—
044Professional consultancy relating to health care; medical counseling; health care consultancy services; medical advisory services relating to medical instruments; medical consulting and advisory services relating to medical instruments regarding obtaining and maintaining commercial product certifications for medical devices; professional medical consultancy relating to health; medical consultations; pharmacy advice, namely, pharmaceutical advice; medical consultancy and information services relating to biopharmaceutical products; medical consultancy and information services relating to medical products; medical consultancy and information services relating to pharmaceutical products; medical consultancy and information services provided via the Internet relating to pharmaceutical products; public health counseling; pharmaceutical advice; medical diagnostic testing, monitoring and reporting services; medical tele-reporting services; medical evaluation services; health care consulting and advisory services in the field of international in vitro diagnostics; medical consulting and advisory services relating to medical devices; medical consulting and advisory services relating to international in vitro diagnostics; health care consulting and advisory services relating to medical devices; medical evaluation services for patients receiving rehabilitation for the purposes of guiding treatment and assessing effectiveness; preparation of reports relating to medical matters, namely, providing medical information to medical professionals in the form of reports in the field of medical productsACTIVE—
045Expert consultancy relating to legal issues; regulatory compliance auditing; legal compliance auditing; regulatory compliance consultation in relation to data protection compliance; reviewing standards and practices to assure compliance with medical device laws and regulations; legal consulting and advisory services relating to legal aspects of international in vitro regulations; legal consulting and advisory services relating to legal aspects of international medical device regulations; legal support servicesACTIVE—

Related trademarks

CopyMark links this record to cited §2(d) serials, the owner's other marks, Nice classes, similar mark names, and recently changed USPTO applications.

Prosecution history

DateCodeEventWhat it means
May 3, 2025FINOFINAL DECISION TRANSACTION PROCESSED BY IB—
Apr 12, 2025FICSFINAL DISPOSITION NOTICE SENT TO IB—
Apr 12, 2025FIMPFINAL DISPOSITION PROCESSED—
Feb 12, 2025FICRFINAL DISPOSITION NOTICE CREATED, TO BE SENT TO IB—
Jan 4, 2025OPNXNOTIFICATION OF POSSIBLE OPPOSITION - PROCESSED BY IB—
Dec 16, 2024OPNSNOTIFICATION OF POSSIBLE OPPOSITION SENT TO IB—
Dec 13, 2024OPNRNOTIFICATION OF POSSIBLE OPPOSITION CREATED, TO BE SENT TO IB—
Nov 12, 2024NRCCNOTICE OF REGISTRATION CONFIRMATION EMAILED—
Nov 12, 2024R.PRREGISTERED-PRINCIPAL REGISTERYour trademark is registered on the Principal Register — the strongest form of federal trademark protection. You may use the ® symbol for the covered goods and services. Maintenance filings (Section 8 and renewals) are required to keep the registration alive.
Aug 27, 2024NPUBOFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED—
Aug 27, 2024PUBOPUBLISHED FOR OPPOSITIONYour mark was published in the USPTO Official Gazette for a 30-day opposition window. During that period, third parties who believe they would be harmed can file an opposition. If no opposition is filed, prosecution usually continues toward registration or a Notice of Allowance.
Aug 7, 2024NONPNOTIFICATION OF NOTICE OF PUBLICATION E-MAILED—
Jul 24, 2024CNSAAPPROVED FOR PUB - PRINCIPAL REGISTER—
Jul 18, 2024TEMETEAS/EMAIL CORRESPONDENCE ENTERED—
Jul 18, 2024CRFACORRESPONDENCE RECEIVED IN LAW OFFICE—
Jul 18, 2024TROATEAS RESPONSE TO OFFICE ACTION RECEIVEDThis event means the applicant filed a response to a USPTO Office Action — typically arguments, amendments, or evidence addressing the examiner's objections. The USPTO will review the response and either allow the mark to proceed or issue another action.
Feb 14, 2024RFNTREFUSAL PROCESSED BY IB—
Jan 19, 2024RFCSNON-FINAL ACTION MAILED - REFUSAL SENT TO IB—
Jan 19, 2024RFRRREFUSAL PROCESSED BY MPU—
Dec 2, 2023RFCRNON-FINAL ACTION (IB REFUSAL) PREPARED FOR REVIEW—
Dec 1, 2023CNRTNON-FINAL ACTION WRITTENA non-final Office Action means the USPTO examining attorney has raised at least one issue with your trademark application but has not made a final decision. You usually have three months to respond with arguments, amendments, or evidence. Missing the deadline can abandon the application.
Dec 1, 2023DOCKASSIGNED TO EXAMINER—
Jul 18, 2023MAFRAPPLICATION FILING RECEIPT MAILED—
Jul 14, 2023NWOSNEW APPLICATION OFFICE SUPPLIED DATA ENTERED—
Jul 13, 2023REPRSN ASSIGNED FOR SECT 66A APPL FROM IB—

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