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Official data from USPTO

AFORTIORI

Did you know this trademark is already registered in United States?

Before investing in name, identity, and promotion, validate collision risk and registration strategy to avoid wasting time and budget.

Active USPTO registrationType: WordOffice: US

Quick snapshot

AFORTIORI

ST13

US500000090893451

Class

35, 41, 42, 45

Filing

90893451

Registration

7123887

Risk and opportunity diagnosis

Executive reading for naming, filing, and monitoring decisions.

Attention: there is active risk

USPTO status

Active USPTO registration

Case type

Application and registration

Recorded events

30

Latest update

09/28/2023

Classification

Registered

Trademark type

Word

Nice classes

35, 41, 42, 45

Filing date

08/20/2021

Registration date

08/01/2023

Expiration date

-

Recommended action

Perform a full collision analysis and validate classes before any filing or trademark investment.

Next step

These are the details of the registration process. Even so, constant monitoring is what ensures peace of mind that your main asset remains protected.

Complete case details

Structured fields from the responsible authority and the official record.

Status date

08/01/2023

Last transaction

09/28/2023

Responsible office

United States Patent and Trademark Office

Status code

700

Official register

Principal Register

Filing basis

Intent to use, Foreign priority

Drawing code

4

Owner type

03

Owner location

Galway, IE

Examiner

FRENCH, CURTIS W

Law office

M60

Current location

PUBLICATION AND ISSUE SECTION

Holders and representatives

Holders

Afortiori Development Limited

Representatives

P. Jay Hines MUNCY, GEISSLER, OLDS & LOWE, P.C.

Technical classification

Nice Classes

Class 35Class 41Class 42Class 45

Vienna Codes

No Vienna codes available.

Goods and services

Class 35

Business strategy and planning services; expert evaluations and reports relating to business matters; collection and analysis of quality metric data for specialist medical professionals for business purposes; 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; data processing; business data analysis in the field of clinical trials; database management; business analysing and compiling of non-technical data in the fields of medicinepharmaceuticalsbiopharmaceuticalsmedical devices and drug approval; business evaluation in the fields of medicinepharmaceuticalsbiopharmaceuticalsmedical devices and drug approval; analysis of business data; analysis of market research data; business research and surveys; conducting surveys for business purposes; market research and analysis; business administration; consultancyinformation and advisory services relating to all of the aforesaid services

Class 41

Publication of on-line reportsarticlesjournals and scientific texts featuring the results of clinical trials; consultancyinformation and advisory services relating to all of the aforesaid services

Class 42

Medical and scientific researchconductingdeveloping and designing clinical trials for others; medical and scientific researchclinical trial monitoring and management services; medical and scientific researchplanningarranging and conducting clinical trials; medical and scientific researchstrategic planning relating to clinical trials; conducting early evaluations in the field of new pharmaceuticals; medical and scientific researchcollection of technical data relating to clinical trialsmedicinepharmaceuticalsbiopharmaceuticalsdrug approvalmedical devices and the development of software applications; evaluation of product development; medical and scientific researchexpert evaluations and reports relating to clinical trials; medical and scientific researchproviding information about the results of clinical trials for pharmaceutical productsincluding biopharmaceuticals and medical devices; providing medical and scientific research information in the field of pharmaceuticals and clinical trials; technical project planning and project management in the fields of medical and scientific researchclinical trialspharmaceuticalsbiopharmaceuticalsdrug approvalmedical devices or software applications; technical analysis and evaluation of clinical reports in the field of medical and scientific research; technical statistical analysis in the field of medical and scientific research; analysismanagement and review of technical data in the fields of medical and scientific researchclinical trialspharmaceuticalsbiopharmaceuticalsdrug approvalmedical devices or software applications; technical testingmeasuringsurvey and evaluation services; pharmaceutical product evaluation; analysis of product development; expert evaluations and reports relating to technical matters in the fields of medical and scientific researchclinical trialspharmaceuticalsbiopharmaceuticalsdrug approvalmedical devices or software applications; database design; maintenance of on-line databases for others; online electronic data storage; measurement evaluation services in the field of medical and scientific research; providing quality assurance services in the fields of medical and scientific researchclinical trialspharmaceuticalsbiopharmaceuticalsdrug approvalmedical devices or software applications; quality management servicesquality evaluation and analysisquality assurancequality controlin the field of medical sciencescientific research and medical consultancy; consulting services for others in the field of designplanning and implementation project management of scientific research or clinical trials

Class 45

Advisory services relating to regulatory affairsregulatory compliance consulting in the field of pharmaceuticalsbiopharmaceuticalsdrug approvalclinical trialsmedicines or medical devices; reviewing standards and practices to assure compliance with laws and regulations; regulatory compliance auditing; consultancyinformation and advisory services relating to all of the aforesaid services

Publications

History of USPTO decisions and trademark events.

30 publications found

TCCA

TEAS CHANGE OF CORRESPONDENCE RECEIVED

09/28/2023

CHAN

APPLICANT/CORRESPONDENCE CHANGES (NON-RESPONSIVE) ENTERED

09/28/2023

COAR

TEAS CHANGE OF OWNER ADDRESS RECEIVED

09/28/2023

NRCC

NOTICE OF REGISTRATION CONFIRMATION EMAILED

08/01/2023

R.PR

REGISTERED-PRINCIPAL REGISTER

08/01/2023

DP1B

1(B) BASIS DELETED; PROCEED TO REGISTRATION

06/28/2023

IUCN

NOTICE OF ALLOWANCE CANCELLED

05/23/2023

D1BR

TEAS DELETE 1(B) BASIS RECEIVED

05/23/2023

NOAM

NOA E-MAILED - SOU REQUIRED FROM APPLICANT

05/23/2023

NPUB

OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED

03/28/2023

PUBO

PUBLISHED FOR OPPOSITION

03/28/2023

NONP

NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED

03/08/2023

FIXD

ELECTRONIC RECORD REVIEW COMPLETE

02/23/2023

ERRR

ON HOLD - ELECTRONIC RECORD REVIEW REQUIRED

02/17/2023

CNSA

APPROVED FOR PUB - PRINCIPAL REGISTER

02/13/2023

TEME

TEAS/EMAIL CORRESPONDENCE ENTERED

02/10/2023

CRFA

CORRESPONDENCE RECEIVED IN LAW OFFICE

02/06/2023

ERSI

TEAS RESPONSE TO SUSPENSION INQUIRY RECEIVED

02/06/2023

GNS3

NOTIFICATION OF LETTER OF SUSPENSION E-MAILED

10/10/2022

GNSL

LETTER OF SUSPENSION E-MAILED

10/10/2022

CNSL

SUSPENSION LETTER WRITTEN

10/10/2022

TEME

TEAS/EMAIL CORRESPONDENCE ENTERED

09/24/2022

CRFA

CORRESPONDENCE RECEIVED IN LAW OFFICE

09/23/2022

TROA

TEAS RESPONSE TO OFFICE ACTION RECEIVED

09/23/2022

GNRN

NOTIFICATION OF NON-FINAL ACTION E-MAILED

05/25/2022

GNRT

NON-FINAL ACTION E-MAILED

05/25/2022

CNRT

NON-FINAL ACTION WRITTEN

05/25/2022

DOCK

ASSIGNED TO EXAMINER

05/23/2022

NWOS

NEW APPLICATION OFFICE SUPPLIED DATA ENTERED

10/07/2021

NWAP

NEW APPLICATION ENTERED

08/24/2021

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