NREP
NEW REPRESENTATIVE AT IB RECEIVED
05/07/2026
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Official data from USPTO
360
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Active USPTO registrationType: CombinedOffice: United States
Risk and opportunity diagnosis
Executive reading for naming, filing, and monitoring decisions.
USPTO status
Active USPTO registration
Case type
Application and registration
Recorded events
32
Latest update
05/08/2026
Trademark type
Combined
Nice classes
9, 41, 42, 45
Filing date
08/16/2023
Registration date
02/18/2025
Expiration date
-
Complete case details
Structured fields from the responsible authority and the official record.
Status date
02/18/2025
Last transaction
05/08/2026
Responsible office
United States Patent and Trademark Office
Status code
700
Official register
Principal Register
Drawing code
3
Owner type
99
Owner location
GB
Examiner
BUSH, KAREN K
Law office
L80
Current location
FILE REPOSITORY (FRANCONIA)
Mark description
The mark consists of "360" in stylized form within a broken circle design.
Holders and representatives
Holders
ARC Regulatory Limited
Representatives
Amy L. Wright Taft Stettinius & Hollister LLP
Technical classification
Nice Classes
Class 9Class 41Class 42Class 45
Vienna Codes
No Vienna codes available.
Goods and services
Class 9
Computerscomputer hardware and computer peripheral devices; computer softwarecomputer application softwareapplication software for mobile devicesall of the aforesaid being downloadable or recorded and for the purpose of accessingnavigatinganalysingupdating and identifying regulatory and legislative requirements in the field of medicinelife sciencespharmaceuticalslaboratory researchlaboratory testing and law; Computer softwarecomputer application softwareapplication software for mobile devicesall 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 medicinelife sciencespharmaceuticalslaboratory researchlaboratory 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 publicationsmagazinesnewslettersperiodicals and brochuresall in the field of medicinelife sciencespharmaceuticalslaboratory researchlaboratory testing and law; downloadable and recorded media including writtenimagevideoaudio and visual contentinfographicsnamely e-booksCDsDVDsaudio and video recordingsdigital image filespodcasts and webinars in the field of medicinelife sciencespharmaceuticalslaboratory researchlaboratory testing and law; downloadable electronic educational materialsbooksaudiobookstextbooksbrochures and video and audio recordings in the field of medicinelife sciencespharmaceuticalslaboratory researchlaboratory testing and law; downloadable data sets relating to regulatory compliance in the medical and life sciences industries
Class 41
Education servicesproviding training coursesonline and live classesseminarswebinarsworkshops and tutorials in the field of medicinelife sciencespharmaceuticalslaboratory researchlaboratory testing and legal industries; providing of training in the field of medicinelife sciencespharmaceuticalslaboratory researchlaboratory testing and legal industries; education services in the medical and life sciences industries; educational services in relation to regulatory complianceissuesupdates and developments; educational services in relation to compliancerisk managementdesign controlquality management solutionsstandard operating proceduresdata integrityunique 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 medicinelife sciencespharmaceuticalslaboratory researchlaboratory testing and legal industries; legal education services; publication of instructional literature; publishingreportingwriting of textsother than publicity texts; arranging and conducting conferencesworkshopsseminarssymposiumcompetitionsconventions and meetings in the medical and life sciences industries; writingreporting and publication of non-downloadable guidelinesreportsdata and case studies relating to the medical and life sciences industries; advisory and consultancy services relating to all above mentioned services
Class 42
Scientifictechnological and industrial analysisresearch and design services in the field of medicinelife sciencespharmaceuticalslaboratory researchlaboratory 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 medicinelife sciencespharmaceuticalslaboratory researchlaboratory testing and legal industries; biological research and medical research; site monitoring services; conducting early evaluations in the field of new pharmaceuticals; pharmaceutical product evaluation; product quality evaluation; quality control services for others; quality management servicesquality evaluation and analysisquality assurance and quality control in the medical and life sciences industries; scientific researchanalysistestingrelated scientific studies in the medical and life sciences industries; consultancy relating to industrial engineering related to medical and life sciences industries; biotechnologybiotechnology 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; testinganalysis 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 accessingnavigatinganalysingupdating and identifying regulatory and legislative requirements in the field of medicinelife sciencespharmaceuticalslaboratory researchlaboratory testing and law; software as a service SaaS for the purpose delivering trainingeducational content and reports in respect of regulatory and legislative requirements in the field of medicinelife sciencespharmaceuticalslaboratory researchlaboratory testing and law; providing onlinenon-downloadable software for the purpose of accessingnavigatinganalysingupdating and identifying regulatory and legislative requirements in the field of medicinelife sciencespharmaceuticalslaboratory researchlaboratory testing and law; providing onlinenon-downloadable software for the purpose delivering trainingeducational content and reports in respect of regulatory and legislative requirements in the field of medicinelife sciencespharmaceuticalslaboratory researchlaboratory testing and law; software designdevelopment and engineering; computer software consultancy; providing onlinenon-downloadable software for generating reports concerning regulatory requirements in the medical and life sciences industries; providing onlinenon-downloadable software for delivering training in relation to regulatory requirements in the medical and life sciences industries; informationconsultancy and advisory services relating to all above mentioned services
Class 45
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 fieldsreviewing standards and practices to assist others with compliance with governmental lawsregulations and rules pertaining to medical devicesmedical technologiesmedicationsbiopharmaceuticalsbiotechnology; 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; informationconsultancy and advisory services relating to all above mentioned services
Publications
History of USPTO decisions and trademark events.
32 publications found
NREP
NEW REPRESENTATIVE AT IB RECEIVED
11/29/2025
FINO
FINAL DECISION TRANSACTION PROCESSED BY IB
09/19/2025
FICS
FINAL DISPOSITION NOTICE SENT TO IB
09/01/2025
FIMP
FINAL DISPOSITION PROCESSED
09/01/2025
FICR
FINAL DISPOSITION NOTICE CREATED, TO BE SENT TO IB
05/18/2025
OPNX
NOTIFICATION OF POSSIBLE OPPOSITION - PROCESSED BY IB
04/04/2025
OPNS
NOTIFICATION OF POSSIBLE OPPOSITION SENT TO IB
03/18/2025
OPNR
NOTIFICATION OF POSSIBLE OPPOSITION CREATED, TO BE SENT TO IB
03/18/2025
NRCC
NOTICE OF REGISTRATION CONFIRMATION EMAILED
02/18/2025
R.PR
REGISTERED-PRINCIPAL REGISTER
02/18/2025
NPUB
OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED
12/31/2024
PUBO
PUBLISHED FOR OPPOSITION
12/31/2024
NONP
NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED
12/25/2024
CNSA
APPROVED FOR PUB - PRINCIPAL REGISTER
12/05/2024
XAEC
EXAMINER'S AMENDMENT ENTERED
11/15/2024
GNEN
NOTIFICATION OF EXAMINERS AMENDMENT E-MAILED
11/15/2024
GNEA
EXAMINERS AMENDMENT E-MAILED
11/15/2024
CNEA
EXAMINERS AMENDMENT -WRITTEN
11/15/2024
TEME
TEAS/EMAIL CORRESPONDENCE ENTERED
10/29/2024
CRFA
CORRESPONDENCE RECEIVED IN LAW OFFICE
10/28/2024
TROA
TEAS RESPONSE TO OFFICE ACTION RECEIVED
10/28/2024
ADCH
CHANGE OF NAME/ADDRESS REC'D FROM IB
06/14/2024
RFNT
REFUSAL PROCESSED BY IB
05/28/2024
RFCS
NON-FINAL ACTION MAILED - REFUSAL SENT TO IB
04/29/2024
RFRR
REFUSAL PROCESSED BY MPU
04/29/2024
RFCR
NON-FINAL ACTION (IB REFUSAL) PREPARED FOR REVIEW
04/19/2024
CNRT
NON-FINAL ACTION WRITTEN
04/18/2024
DOCK
ASSIGNED TO EXAMINER
04/17/2024
MAFR
APPLICATION FILING RECEIPT MAILED
10/24/2023
NWOS
NEW APPLICATION OFFICE SUPPLIED DATA ENTERED
10/20/2023
REPR
SN ASSIGNED FOR SECT 66A APPL FROM IB
10/19/2023
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