USPTO serial 79353095
TRIALSCOPE ATLAS
Reviewed by CopyMark Law Group
- Filing date
- Status date
- Registration date
- —
- Examiner
- SWAIN, MICHELE LYNN
- Law office
- TMO LAW OFFICE 116 - EXAMINING ATTORNEY ASSIGNED
What this means
These status codes mean the trademark application is abandoned and no longer pending. Common reasons include missing an Office Action response (600), filing without a valid basis (602), express abandonment by the applicant (604), or failure to respond to an examiner's inquiry (618). Revival may be possible in limited circumstances. If abandonment was unintentional, consult counsel about a petition to revive. Otherwise file a new application if protection is still needed.
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Owner
Attorney of record
The USPTO lists this attorney as the applicant's representative for correspondence on this application.
William C. Wright
William C. Wright Epstein Drangel LLP60 East 42nd Street, Suite 1250New York, NY 10165UNITED STATESGoods and services
| Class | Description | Status | First use |
|---|---|---|---|
| 009 | Scientific, research, navigation, surveying, photographic, cinematographic, audio-visual, optical, weighing, measuring, signalling, detecting, testing, inspecting, life-saving and teaching apparatus and instruments; apparatus and instruments for conducting, switching, transforming, accumulating, regulating or controlling the distribution or use of electricity; apparatus and instruments for recording, transmitting, reproducing or processing sound, images or data; recorded and downloadable media, computer software, blank digital or analogue recording and storage media; mechanisms for coin-operated apparatus; cash registers, calculating devices; computers and computer peripheral devices; diving suits, divers' masks, ear plugs for divers, nose clips for divers and swimmers, gloves for divers, breathing apparatus for underwater swimming; fire-extinguishing apparatus; cases and bags adapted for laptops; cases for smartphones; computer hardware; computer memory devices and media; computer software; databases; downloadable multimedia files; downloadable publications; podcasts; software featuring information and intelligence data; software featuring searchable databases; software for business management; software for data capture, data analysis, and data processing; software for document management; software for research management; teaching apparatus; USB flash drives; computer software to assist with clinical trial disclosure management, clinical trial communications, patient referrals, clinical trial recruitment, clinical trial data, managing clinical data requests and clinical record management; computer software to assist with sharing of clinical data and clinical trial results, accelerate clinical study recruitment, optimise clinical study spending, build clinical trial awareness and reputation, automate and simplify global clinical trial disclosure, safeguard regulatory compliance in relation to clinical trials, mitigate risk in clinical trials, assist with disclosure activities and compliance in relation to clinical trials, fulfil and manage clinical data requests, track key performance indicators in relation to clinical trials, track industry benchmarks in relation to clinical trials, and provide clinical trial results summaries; database server software featuring clinical trial data; database server software featuring data in relation to sharing of clinical data and clinical trial results, acceleration of clinical study recruitment, optimisation of clinical study spending, building clinical trial awareness and reputation, automating and simplifying global clinical trial disclosure, safeguarding regulatory compliance in relation to clinical trials, mitigating risk in clinical trials, assisting with disclosure activities and compliance in relation to clinical trials, fulfilling and managing clinical data requests, tracking key performance indicators in relation to clinical trials, tracking industry benchmarks in relation to clinical trials, and providing clinical trial results summaries; database server software featuring information in relation to clinical trial disclosure management, clinical trial communications, patient referrals, clinical trial recruitment, clinical trial data, managing clinical data requests and clinical record management; downloadable publications in relation to clinical trial disclosure management, clinical trial communications, patient referrals, clinical trial recruitment, clinical trial data, managing clinical data requests and clinical record management; downloadable publications in relation to sharing of clinical data and clinical trial results, acceleration of clinical study recruitment, optimisation of clinical study spending, building clinical trial awareness and reputation, automating and simplifying global clinical trial disclosure, safeguarding regulatory compliance in relation to clinical trials, mitigating risk in clinical trials, assisting with disclosure activities and compliance in relation to clinical trials, fulfilling and managing clinical data requests, tracking key performance indicators in relation to clinical trials, tracking industry benchmarks in relation to clinical trials, and providing clinical trial results summaries; computer software for use in the management of clinical trials; computer software for use in relation to pharmaceutical and biotech compliance activities; computer software for the recording and processing of clinical trial disclosure rules; computer software for the recording and processing of clinical data; computer software featuring advice and guidance on compulsory and voluntary disclosure requirements in relation to clinical trials; databases featuring information in relation to the management of clinical trials; databases featuring information in relation to pharmaceutical and biotech compliance activities; databases featuring information on clinical trial disclosure rules; databases featuring information on clinical data; databases featuring advice and guidance on compulsory and voluntary disclosure requirements in relation to clinical trials; downloadable publications concerning the management of clinical trials; downloadable publications relating to pharmaceutical and biotech compliance activities; downloadable publications concerning clinical trial disclosure rules; downloadable publications concerning clinical data; downloadable publications featuring advice and guidance on compulsory and voluntary disclosure requirements in relation to clinical trials; parts and fittings for all of the aforesaid goods | ACTIVE | — |
| 041 | Education; providing of training; entertainment; sporting and cultural activities; arranging and conducting of colloquiums, conferences, congresses, seminars, symposiums and training workshops; arranging and conducting of exhibitions for cultural or educational purposes; arranging and conducting of in-person forums; book club services; books (publication of -); editing of periodicals, journals and publications; news reporting; preparation of educational courses and examinations; production of podcasts; production of webcasts; providing on-line electronic publications [not downloadable]; providing on-line training; provision of news online, gathering and dissemination of news; provision of news online; publication of booklets, brochures and fact sheets; publication of books and journals; publication of data reports, analysis and infographics; publication of texts [other than publicity texts]; publishing reviews of publications provided online, from a database, via the internet or any other communications network; providing online non-downloadable publications in relation to clinical trial disclosure management, clinical trial communications, patient referrals, clinical trial recruitment, clinical trial data, managing clinical data requests and clinical record management; providing online non-downloadable publications in relation to clinical data and clinical trial results, acceleration of clinical study recruitment, optimisation of clinical study spending, building clinical trial awareness and reputation, automating and simplifying global clinical trial disclosure, safeguarding regulatory compliance in relation to clinical trials, mitigating risk in clinical trials, assisting with disclosure activities and compliance in relation to clinical trials, fulfilling and managing clinical data requests, tracking key performance indicators in relation to clinical trials, tracking industry benchmarks in relation to clinical trials, and providing clinical trial results summaries; education in relation to clinical trials; education in relation to pharmaceutical and biotech compliance activities; education in relation to clinical trial disclosure rules; education in relation to clinical data; education in relation to clinical trials; education in relation to clinical trial disclosure management, clinical trial communications, patient referrals, clinical trial recruitment, clinical trial data, managing clinical data requests and clinical record management; education in relation to clinical data and clinical trial results, acceleration of clinical study recruitment, optimisation of clinical study spending, building clinical trial awareness and reputation, automating and simplifying global clinical trial disclosure, safeguarding regulatory compliance in relation to clinical trials, mitigating risk in clinical trials, assisting with disclosure activities and compliance in relation to clinical trials, fulfilling and managing clinical data requests, tracking key performance indicators in relation to clinical trials, tracking industry benchmarks in relation to clinical trials, and providing clinical trial results summaries; providing of training in relation to clinical trials; providing of training in relation to pharmaceutical and biotech compliance activities; providing of training in relation to clinical trial disclosure rules; providing of training in relation to clinical data; providing of training in relation to clinical trials; providing of training in relation to clinical trial disclosure management, clinical trial communications, patient referrals, clinical trial recruitment, clinical trial data, managing clinical data requests and clinical record management; providing of training in relation to clinical data and clinical trial results, acceleration of clinical study recruitment, optimisation of clinical study spending, building clinical trial awareness and reputation, automating and simplifying global clinical trial disclosure, safeguarding regulatory compliance in relation to clinical trials, mitigating risk in clinical trials, assisting with disclosure activities and compliance in relation to clinical trials, fulfilling and managing clinical data requests, tracking key performance indicators in relation to clinical trials, tracking industry benchmarks in relation to clinical trials, and providing clinical trial results summaries; arranging and conducting of conferences, educational seminars and training workshops in relation clinical trials; arranging and conducting of conferences, educational seminars and training workshops in relation to pharmaceutical and biotech compliance activities; arranging and conducting of conferences, educational seminars and training workshops in relation to clinical trial disclosure rules; arranging and conducting of conferences, educational seminars and training workshops in relation to clinical data; arranging and conducting of conferences, educational seminars and training workshops in relation to clinical trials; arranging and conducting of conferences, educational seminars and training workshops in relation to clinical trial disclosure management, clinical trial communications, patient referrals, clinical trial recruitment, clinical trial data, managing clinical data requests and clinical record management; arranging and conducting of conferences, educational seminars and training workshops in relation to clinical data and clinical trial results, acceleration of clinical study recruitment, optimisation of clinical study spending, building clinical trial awareness and reputation, automating and simplifying global clinical trial disclosure, safeguarding regulatory compliance in relation to clinical trials, mitigating risk in clinical trials, assisting with disclosure activities and compliance in relation to clinical trials, fulfilling and managing clinical data requests, tracking key performance indicators in relation to clinical trials, tracking industry benchmarks in relation to clinical trials, and providing clinical trial results summaries; information, consultancy and advisory services relating to all the aforesaid services including such services provided on-line or via the Internet | ACTIVE | — |
| 042 | Scientific and technological services and research and design relating thereto; industrial analysis, industrial research and industrial design services; quality control and authentication services; design and development of computer hardware and software; clinical trials; computer network services; computer programming; computer programming for data processing and communication systems; computer programming services for the protection of software; computer project management in the field of electronic data processing [EDP]; computer services for securing computer data; provision of customised web pages featuring user-defined information, personal profiles and information [computer services]; consultancy and information services relating to information technology; database design and development; design and development of systems for data input, output, processing, display and storage; design and development of testing and analysis methods; hosting computer application software; hosting of digital content, namely, online journals and blogs; hosting online web facilities for others for organising and conducting online meetings, gatherings, and interactive discussions; hosting web sites; hosting weblogs [blogs]; industrial analysis and research services; pharmaceutical research; in vitro analysis for medical and pharmaceutical research services; platform as a service; providing scientific research information and results from an on-line searchable database; providing search engines for obtaining data on a global computer network; providing software for generating data reports for use in publishing and printing; software as a service; technical research; hosting of digital content, namely, online journals and blogs in relation to clinical trial disclosure management, clinical trial communications, patient referrals, clinical trial recruitment, clinical trial data, managing clinical data requests and clinical record management; software as a service to assist with clinical trial disclosure management, clinical trial communications, patient referrals, clinical trial recruitment, clinical trial data, managing clinical data requests and clinical record management; hosting of digital content, namely, online journals and blogs in relation to sharing of clinical data and clinical trial results, acceleration of clinical study recruitment, optimisation of clinical study spending, building clinical trial awareness and reputation, automating and simplifying global clinical trial disclosure, safeguarding regulatory compliance in relation to clinical trials, mitigating risk in clinical trials, assisting with disclosure activities and compliance in relation to clinical trials, fulfilling and managing clinical data requests, tracking key performance indicators in relation to clinical trials, tracking industry benchmarks in relation to clinical trials, and providing clinical trial results summaries; software as a service to assist with sharing of clinical data and clinical trial results, accelerate clinical study recruitment, optimise clinical study spending, build clinical trial awareness and reputation, automate and simplify global clinical trial disclosure, safeguard regulatory compliance in relation to clinical trials, mitigate risk in clinical trials, assist with disclosure activities and compliance in relation to clinical trials, fulfil and manage clinical data requests, track key performance indicators in relation to clinical trials, track industry benchmarks in relation to clinical trials, and provide clinical trial results summaries; hosting of digital content, namely, online journals and blogs in relation to the management of clinical trials; hosting of digital content, namely, online journals and blogs in relation to pharmaceutical and biotech compliance activities; hosting of digital content, namely, online journals and blogs in relation to recording and processing of clinical trial disclosure rules; hosting of digital content, namely, online journals and blogs in relation to the recording and processing of clinical data; hosting of digital content, namely, online journals and blogs providing advice and guidance on compulsory and voluntary disclosure requirements in relation to clinical trials; software as a service to assist with the management of clinical trials; software as a service to assist with pharmaceutical and biotech compliance activities; software as a service to assist with recording and processing of clinical trial disclosure rules; software as a service to assist with recording and processing of clinical data; software as a service to provide advice and guidance on compulsory and voluntary disclosure requirements in relation to clinical trials; information, consultancy, and advisory services relating to all the aforesaid services including such services provided on-line or via the Internet | ACTIVE | — |
| 044 | Medical services; veterinary services; hygienic and beauty care for human beings or animals; agriculture, aquaculture, horticulture and forestry services; advisory services relating to pharmaceuticals; agriculture, horticulture and forestry services; beauty therapy services; cosmetic treatment services; dentistry services; dispensing of pharmaceuticals; healthcare services; health risk assessment surveys; hygienic and beauty care for human beings or animals; issuing of medical reports; medical analysis services; medical services; medical testing services; surgical treatment services; veterinary services; information, consultancy, and advisory services relating to all the aforesaid services including such services provided on-line or via the Internet | ACTIVE | — |
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.
- Other trademarks owned by Informa Business Intelligence, Inc.
- Other trademarks owned by Caerus US 1 Inc.
- Other trademarks in Class 009
- Other trademarks in Class 041
- Other trademarks in Class 042
- Other trademarks in Class 044
- Similar marks named TRIALSCOPE ATLAS
- Recently changed USPTO trademarks
- Recently filed trademarks
- Browse all trademark records
Prosecution history
| Date | Code | Event | What it means |
|---|---|---|---|
| Apr 24, 2025 | NREP | NEW REPRESENTATIVE AT IB RECEIVED | — |
| Aug 24, 2024 | FINT | FINAL DECISION TRANSACTION PROCESSED BY IB | — |
| Aug 2, 2024 | FICS | FINAL DISPOSITION NOTICE SENT TO IB | — |
| Aug 2, 2024 | FICR | FINAL DISPOSITION NOTICE CREATED, TO BE SENT TO IB | — |
| Apr 8, 2024 | OPNX | NOTIFICATION OF POSSIBLE OPPOSITION - PROCESSED BY IB | — |
| Mar 20, 2024 | OPNS | NOTIFICATION OF POSSIBLE OPPOSITION SENT TO IB | — |
| Mar 20, 2024 | OPNR | NOTIFICATION OF POSSIBLE OPPOSITION CREATED, TO BE SENT TO IB | — |
| Aug 1, 2023 | MAB2 | ABANDONMENT NOTICE E-MAILED - FAILURE TO RESPOND | The trademark application was abandoned because a required response or document was not filed by the deadline — usually a missed Office Action response. The application is dead unless a petition to revive is granted within a limited time. |
| Aug 1, 2023 | MAB2 | ABANDONMENT NOTICE MAILED - FAILURE TO RESPOND | The trademark application was abandoned because a required response or document was not filed by the deadline — usually a missed Office Action response. The application is dead unless a petition to revive is granted within a limited time. |
| Aug 1, 2023 | ABN2 | ABANDONMENT - FAILURE TO RESPOND OR LATE RESPONSE | The trademark application was abandoned because a required response or document was not filed by the deadline — usually a missed Office Action response. The application is dead unless a petition to revive is granted within a limited time. |
| Jul 26, 2023 | TCCA | TEAS CHANGE OF CORRESPONDENCE RECEIVED | — |
| Jul 26, 2023 | ARAA | ATTORNEY/DOM.REP.REVOKED AND/OR APPOINTED | This 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. |
| Jul 26, 2023 | REAP | TEAS REVOKE/APP/CHANGE ADDR OF ATTY/DOM REP RECEIVED | — |
| Jul 26, 2023 | CHAN | APPLICANT/CORRESPONDENCE CHANGES (NON-RESPONSIVE) ENTERED | — |
| Jul 26, 2023 | COAR | TEAS CHANGE OF OWNER ADDRESS RECEIVED | — |
| Feb 15, 2023 | RFNT | REFUSAL PROCESSED BY IB | — |
| Feb 4, 2023 | CHLD | CHANGE OF OWNER RECEIVED FROM IB | — |
| Jan 12, 2023 | RFCS | NON-FINAL ACTION MAILED - REFUSAL SENT TO IB | — |
| Jan 12, 2023 | RFRR | REFUSAL PROCESSED BY MPU | — |
| Nov 3, 2022 | RFCR | NON-FINAL ACTION (IB REFUSAL) PREPARED FOR REVIEW | — |
| Nov 2, 2022 | CNRT | NON-FINAL ACTION WRITTEN | A 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. |
| Oct 27, 2022 | DOCK | ASSIGNED TO EXAMINER | — |
| Oct 25, 2022 | MAFR | APPLICATION FILING RECEIPT MAILED | — |
| Oct 21, 2022 | NWOS | NEW APPLICATION OFFICE SUPPLIED DATA ENTERED | — |
| Oct 20, 2022 | REPR | SN ASSIGNED FOR SECT 66A APPL FROM IB | — |