Serial #79390896
LIVE

Serial Number

79390896

Owner

ARC Regulatory Limited

Attorney

Amy L. Wright

Filing Date

Aug 16, 2023

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Serial #79390896 Trademark

Serial Number: 79390896 • Registration: 7691423

Serial #79390896 is a trademark filed by ARC Regulatory Limited on August 16, 2023. The trademark is classified under Class 9 (Computers & Electronics), Class 41 (Education & Entertainment), Class 42 (Computer & Scientific), Class 44 (Medical Services), Class 45 (Legal & Security Services), Class 35 (Advertising & Business). The application is currently registered and active.

Owner Contact Info

ARC Regulatory Limited (4 trademarks)

Unit 1a Concourse Building 1,

Entity Type: 99

Trademark Details

Filing Date

August 16, 2023

Registration Date

February 18, 2025

Published for Opposition

December 31, 2024

Goods & Services

Advertising; business management, organization and administration; providng office functions; market research, prospecting and analysis; collection, compilation, analysis, reporting and dissemination of statistics, data and information; marketing assistance and consultancy; business consultancy services relating to the supply of quality management systems; consultancy relating to data processing; business consulting services in the medical and life sciences industries; business advisory, development, and strategic planning services provided to companies for business purposes in the medical and life sciences industries; business consulting and management in the field of clinical trials, namely, clinical data and regulatory submission management on behalf of medical, biopharmaceutical and biotechnology companies to assist them with clinical research, clinical trials and applications for drug approval; regulatory submission business management, in the nature of administrative assistance, namely, assisting others in preparing and filing applications for regulatory approval of medical devices, medical technologies, medications, pharmaceuticals, and biotechnology; providing information online regarding regulatory submission business management in the nature of administrative assistance; commercial consultancy relating to the development and marketing of medical apparatus and devices; advice on the implementation of communication strategies relating to medical devices; business and advisory consultancy services relating to obtaining and maintaining commercial product certifications.

Clinical medical consultation services; medical information; professional consultancy relating to health care; advisory services relating to medical and surgical instruments and devices; consulting and advisory services relating to obtaining and maintaining commercial product certifications for medical and surgical instruments and devices; consultancy and information services relating to medical, pharmaceutical and biopharmaceutical products; consulting and advisory services relating to the European union in vitro diagnostic regulation (IVDR); consulting and advisory services relating to the European union medical device regulation (MDR); consulting and advisory services relating to medical aspects of the European union in vitro diagnostic regulation (IVDR); consulting and advisory services relating to medical aspects of the European union medical device regulation (MDR); preparation of reports relating to medical matters; preparation of clinical and performance evaluation reports; preparation of clinical and performance evaluation reports for medical devices; information, consultancy and advisory services relating to all above mentioned services.

Education services, namely, providing training courses, online and live classes, seminars, webinars, workshops and tutorials in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and legal industries; providing of training in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and legal industries; education services in the medical and life sciences industries; educational services in relation to regulatory compliance, issues, updates and developments; educational services in relation to good practice compliance, risk management, design control, quality management solutions, standard operating procedures, data integrity, unique device identification and regulatory readiness; education and training in relation to compliance and legal aspects of the European union in vitro diagnostic regulation; education services relating to quality services in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and legal industries; legal education services; publication of instructional literature; publishing, reporting, and writing of texts, other than publicity texts; arranging and conducting conferences, workshops, seminars, symposia, competitions, conventions and meetings in the medical and life sciences industries; writing, reporting and publication of non-downloadable guidelines, reports, data and case studies relating to the medical and life sciences industries; advisory and consultancy services relating to all above mentioned services.

Legal services; regulatory and legal compliance auditing; advisory services relating to regulatory affairs; expert consultancy relating to legal issues regulatory compliance consulting services in the life sciences fields; regulatory compliance consulting services in the life sciences fields namely, reviewing standards and practices to assist others with compliance with governmental laws, regulations and rules pertaining to medical devices, medical technologies, medications, biopharmaceuticals, and biotechnology; consulting and advisory services relating to legal aspects of the European Union In vitro Diagnostic Regulation (IVDR); consulting and advisory services relating to legal aspects of the European Union Medical Device Regulation (MDR); legal support services; information, consultancy and advisory services relating to all above mentioned services.

Computers, computer hardware and computer peripheral devices; computer software; computer application software; application software for mobile devices, all of the aforesaid being downloadable or recorded and for the purpose of accessing, navigating, analysing, updating and identifying regulatory and legislative requirements in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; Computer software; computer application software; application software for mobile devices, all of the aforesaid being downloadable or recorded and for the purpose of delivering training and educational content in respect of regulatory and legislative requirements in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; downloadable and recorded computer software for generating reports concerning regulatory requirements in the medical and life sciences industries; downloadable and recorded computer software for delivering training in relation to regulatory requirements in the medical and life sciences industries; downloadable publications, namely, magazines, newsletters, periodicals and brochures, all in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; downloadable and recorded media including written, image, video, audio and visual content, and infographics, namely, e-books, CDs, DVDs, audio and video recordings, digital image files, podcasts and webinars in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; downloadable educational materials, namely, books, audiobooks, textbooks, brochures and video and audio recordings in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; downloadable electronic educational materials; downloadable data sets; downloadable data sets relating to regulatory compliance in the medical and life sciences industries

Scientific, technological and industrial analysis, research and design services in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and legal industries; conducting and designing clinical trials for others; laboratory testing of materials; consultancy services related to laboratory testing of materials; clinical research in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and legal industries; biological research and medical research; site monitoring services; analysis and evaluation of product development; analysis and evaluation of product design; conducting early evaluations in the field of new pharmaceuticals; pharmaceutical product evaluation; product quality evaluation; quality control services for others; quality management services, namely, quality evaluation and analysis, quality assurance and quality control in the medical and life sciences industries; scientific research, analysis, testing, and related scientific studies in the medical and life sciences industries; consulting services in the medical and life sciences industries; biotechnology, biotechnology research consulting services; pharmaceutical research and product development for use in manufacturing; consulting services for others in the field of designing pre-clinical and clinical studies and trials for others; technical writing; technical writing for others; testing, analysis and evaluation of the services of others for the purpose of certification; testing of apparatus in the field of medical devices for certification purposes; electronic data storage; software as a service [SaaS] for the purpose of accessing, navigating, analysing, updating and identifying regulatory and legislative requirements in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; software as a service [SaaS] for the purpose delivering training, educational content and reports in respect of regulatory and legislative requirements in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; providing online, non-downloadable software for the purpose of accessing, navigating, analysing, updating and identifying regulatory and legislative requirements in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; providing online, non-downloadable software for the purpose delivering training, educational content and reports in respect of regulatory and legislative requirements in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; software design, development and engineering; computer software consultancy; providing online, non-downloadable software for generating reports concerning regulatory requirements in the medical and life sciences industries; providing online, non-downloadable software for delivering training in relation to regulatory requirements in the medical and life sciences industries; information, consultancy and advisory services relating to all above mentioned services.

Filing History

NEW REPRESENTATIVE AT IB RECEIVED
May 7, 2026 NREP
NEW REPRESENTATIVE AT IB RECEIVED
Nov 29, 2025 NREP
FINAL DECISION TRANSACTION PROCESSED BY IB
Sep 19, 2025 FINO
FINAL DISPOSITION NOTICE SENT TO IB
Sep 2, 2025 FICS
FINAL DISPOSITION PROCESSED
Sep 1, 2025 FIMP
NOTIFICATION OF POSSIBLE OPPOSITION - PROCESSED BY IB
Aug 22, 2025 OPNX
NOTIFICATION OF POSSIBLE OPPOSITION SENT TO IB
Aug 6, 2025 OPNS
NOTIFICATION OF POSSIBLE OPPOSITION CREATED, TO BE SENT TO IB
Aug 6, 2025 OPNR
FINAL DISPOSITION NOTICE CREATED, TO BE SENT TO IB
May 19, 2025 FICR
NOTICE OF REGISTRATION CONFIRMATION EMAILED
Feb 18, 2025 NRCC
REGISTERED-PRINCIPAL REGISTER
Feb 18, 2025 R.PR
OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED
Dec 31, 2024 NPUB
PUBLISHED FOR OPPOSITION
Dec 31, 2024 PUBO
NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED
Dec 25, 2024 NONP
APPROVED FOR PUB - PRINCIPAL REGISTER
Dec 5, 2024 CNSA
EXAMINER'S AMENDMENT ENTERED
Nov 15, 2024 XAEC
NOTIFICATION OF EXAMINERS AMENDMENT E-MAILED
Nov 15, 2024 GNEN
EXAMINERS AMENDMENT E-MAILED
Nov 15, 2024 GNEA
EXAMINERS AMENDMENT -WRITTEN
Nov 15, 2024 CNEA
TEAS/EMAIL CORRESPONDENCE ENTERED
Oct 29, 2024 TEME
CORRESPONDENCE RECEIVED IN LAW OFFICE
Oct 29, 2024 CRFA
TEAS RESPONSE TO OFFICE ACTION RECEIVED
Oct 29, 2024 TROA
CHANGE OF NAME/ADDRESS REC'D FROM IB
Jun 14, 2024 ADCH
REFUSAL PROCESSED BY IB
May 28, 2024 RFNT
NON-FINAL ACTION MAILED - REFUSAL SENT TO IB
Apr 30, 2024 RFCS
REFUSAL PROCESSED BY MPU
Apr 30, 2024 RFRR
APPLICATION FILING RECEIPT MAILED
Apr 24, 2024 MAFR
NON-FINAL ACTION (IB REFUSAL) PREPARED FOR REVIEW
Apr 20, 2024 RFCR
NON-FINAL ACTION WRITTEN
Apr 19, 2024 CNRT
ASSIGNED TO EXAMINER
Apr 17, 2024 DOCK
NEW APPLICATION OFFICE SUPPLIED DATA ENTERED
Mar 13, 2024 NWOS
NEW APPLICATION OFFICE SUPPLIED DATA ENTERED
Mar 10, 2024 NWOS
NEW APPLICATION OFFICE SUPPLIED DATA ENTERED
Mar 10, 2024 NWOS
SN ASSIGNED FOR SECT 66A APPL FROM IB
Mar 7, 2024 REPR