USPTO serial 90156971
Reviewed by CopyMark Law Group
This registration is in, or will soon enter, a USPTO maintenance window. Missing a Section 8 or Section 9 filing can cancel the registration.
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Carrie Webb Olson
Carrie Webb Olson DAY PITNEY LLPOne Federal Street - 29th FloorBoston, MA 02110United States| Class | Description | Status | First use |
|---|---|---|---|
| 035 | On-line retail ordering services featuring clinical metadata management computer software for use in relation to clinical trials, clinical management computer software for use in relation to clinical trials, computer software for use in exclusively collecting, storing, controlling, managing and submitting of clinical metadata and clinical data in relation to clinical trials, database management computer software for use exclusively in relation to clinical trials, computer software to allow users to collect, store, control, manage and submit clinical metadata and clinical data in relation to clinical trials, computer databases for collecting, storing, controlling, managing and submitting clinical data in relation to clinical trials, computer software designed to ensure that clinical metadata and clinical data meets the regulations and standards required by international and government agencies in relation to clinical trials, computer software used by pharmaceutical companies, biotechnology companies, medical device manufacturers, and contract research organizations to help collect the required clinical data and meet the required standards for data collection, tabulation, analysis, and submission for clinical trials, all of the aforesaid computer software being used in relation to clinical trials only | ACTIVE | — |
| 041 | Providing training services to enable pharmaceutical companies, biotechnology companies, medical device manufacturers, and contract research organizations to use clinical metadata management software platforms for managing clinical trial metadata and clinical trial data; providing training services to enable pharmaceutical companies, biotechnology companies, medical device manufacturers, and contract research organizations to collect the required clinical data and meet the regulations and standards required by international and government agencies for data collection, tabulation, analysis, and submission for clinical trials; providing training services in relation to the use of clinical metadata management computer software for use in relation to clinical trials; providing training services in relation to the use of clinical management computer software for use in relation to clinical trials; all of the aforesaid training services being used in relation to clinical trials only | ACTIVE | — |
| 042 | Providing temporary use of on-line non-downloadable clinical metadata management computer software for use in relation to clinical trials; providing temporary use of on-line non-downloadable clinical management computer software for use in relation to clinical trials; providing temporary use of on-line non-downloadable computer software for use in exclusively collecting, storing, controlling, managing and submitting of clinical metadata and clinical data in relation to clinical trials; providing temporary use of on-line non-downloadable database management computer software for use exclusively in relation to clinical trials; providing temporary use of on-line non-downloadable computer software to allow users to collect, store, control, manage and submit clinical metadata and clinical data in relation to clinical trials; providing on-line computer databases for collecting, storing, controlling, managing and submitting clinical data in relation to clinical trials; providing temporary use of on-line non-downloadable computer software designed to ensure that clinical metadata and clinical data meets the regulations and standards required by international and government agencies in relation to clinical trials; providing temporary use of on-line non-downloadable computer software used by pharmaceutical companies, biotechnology companies, medical device manufacturers, and contract research organizations to help collect the required clinical data and meet the required standards for data collection, tabulation, analysis, and submission for clinical trials; design and development of computer software exclusively for managing clinical metadata and clinical data in clinical trials; designing, creating and maintaining web pages exclusively in connection with collecting, storing, controlling and managing clinical metadata and clinical data, to meet the regulations and standards required by international and government agencies in conducting clinical trials; all of the aforesaid software services being used in relation to clinical trials only; technical support services, namely, troubleshooting of computer software problems related to clinical metadata management software platforms for managing clinical trial metadata and clinical trial data; providing medical and scientific research information in the field of clinical trials to enable pharmaceutical companies, biotechnology companies, medical device manufacturers, and contract research organizations to collect the required clinical data and meet the regulations and standards required by international and government agencies for data collection, tabulation, analysis, and submission for clinical trials; technical support services, namely, troubleshooting of computer software problems related to clinical metadata management computer software for use in relation to clinical trials; technical support services, namely, troubleshooting of computer software problems related to clinical management computer software for use in relation to clinical trials; all of the aforesaid information and support services being used in relation to clinical trials only | ACTIVE | — |
CopyMark links this record to cited §2(d) serials, the owner's other marks, Nice classes, similar mark names, and recently changed USPTO applications.
| Date | Code | Event | What it means |
|---|---|---|---|
| May 7, 2025 | EWAF | TEAS WITHDRAWAL OF ATTORNEY RECEIVED-FIRM RETAINS | — |
| May 7, 2025 | TCCA | TEAS CHANGE OF CORRESPONDENCE RECEIVED | — |
| May 7, 2025 | ECDR | TEAS CHANGE OF DOMESTIC REPRESENTATIVES ADDRESS | — |
| May 7, 2025 | 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. |
| May 7, 2025 | REAP | TEAS REVOKE/APP/CHANGE ADDR OF ATTY/DOM REP RECEIVED | — |
| May 7, 2025 | CHAN | APPLICANT/CORRESPONDENCE CHANGES (NON-RESPONSIVE) ENTERED | — |
| May 7, 2025 | COAR | TEAS CHANGE OF OWNER ADDRESS RECEIVED | — |
| Oct 26, 2021 | R.PR | REGISTERED-PRINCIPAL REGISTER | Your 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 10, 2021 | NPUB | OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED | — |
| Aug 10, 2021 | PUBO | PUBLISHED FOR OPPOSITION | Your 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. |
| Jul 21, 2021 | NONP | NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED | — |
| Jul 1, 2021 | CNSA | APPROVED FOR PUB - PRINCIPAL REGISTER | — |
| Jul 1, 2021 | XAEC | EXAMINER'S AMENDMENT ENTERED | — |
| Jul 1, 2021 | GNEN | NOTIFICATION OF EXAMINERS AMENDMENT E-MAILED | — |
| Jul 1, 2021 | GNEA | EXAMINERS AMENDMENT E-MAILED | — |
| Jul 1, 2021 | CNEA | EXAMINERS AMENDMENT -WRITTEN | — |
| Jun 21, 2021 | TEME | TEAS/EMAIL CORRESPONDENCE ENTERED | — |
| Jun 21, 2021 | CRFA | CORRESPONDENCE RECEIVED IN LAW OFFICE | — |
| Jun 17, 2021 | ALIE | ASSIGNED TO LIE | — |
| Mar 29, 2021 | ERSI | TEAS RESPONSE TO SUSPENSION INQUIRY RECEIVED | — |
| Mar 25, 2021 | GNS3 | NOTIFICATION OF LETTER OF SUSPENSION E-MAILED | — |
| Mar 25, 2021 | GNSL | LETTER OF SUSPENSION E-MAILED | — |
| Mar 25, 2021 | CNSL | SUSPENSION LETTER WRITTEN | — |
| Mar 4, 2021 | TEME | TEAS/EMAIL CORRESPONDENCE ENTERED | — |
| Mar 3, 2021 | CRFA | CORRESPONDENCE RECEIVED IN LAW OFFICE | — |
| Mar 3, 2021 | TROA | TEAS RESPONSE TO OFFICE ACTION RECEIVED | 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. |
| Dec 22, 2020 | GNRN | NOTIFICATION OF NON-FINAL ACTION E-MAILED | 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. |
| Dec 22, 2020 | GNRT | NON-FINAL ACTION E-MAILED | 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. |
| Dec 22, 2020 | 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. |
| Dec 21, 2020 | DOCK | ASSIGNED TO EXAMINER | — |
| Oct 8, 2020 | NWOS | NEW APPLICATION OFFICE SUPPLIED DATA ENTERED | — |
| Sep 7, 2020 | NWAP | NEW APPLICATION ENTERED | — |