Legal Representation
Attorney
Carrie Webb Olson
USPTO Deadlines
Next Deadline
788 days remaining
Section 8 (6-Year) Declaration Due (Based on registration date 2021-09-14)
Due Date
September 14, 2027
Grace Period Ends
March 14, 2028
Additional deadlines exist. Contact your attorney for complete deadline information.
Application History
37 eventsDate | Code | Type | Description | Documents |
---|---|---|---|---|
May 7, 2025 | TCCA | I | TEAS CHANGE OF CORRESPONDENCE RECEIVED | Loading... |
May 7, 2025 | ECDR | I | TEAS CHANGE OF DOMESTIC REPRESENTATIVES ADDRESS | Loading... |
May 7, 2025 | REAP | I | TEAS REVOKE/APP/CHANGE ADDR OF ATTY/DOM REP RECEIVED | Loading... |
May 7, 2025 | CHAN | I | APPLICANT/CORRESPONDENCE CHANGES (NON-RESPONSIVE) ENTERED | Loading... |
May 7, 2025 | ARAA | I | ATTORNEY/DOM.REP.REVOKED AND/OR APPOINTED | Loading... |
May 7, 2025 | EWAF | I | TEAS WITHDRAWAL OF ATTORNEY RECEIVED-FIRM RETAINS | Loading... |
May 7, 2025 | COAR | I | TEAS CHANGE OF OWNER ADDRESS RECEIVED | Loading... |
Sep 14, 2021 | R.PR | A | REGISTERED-PRINCIPAL REGISTER | Loading... |
Aug 12, 2021 | DP1B | I | 1(B) BASIS DELETED; PROCEED TO REGISTRATION | Loading... |
Aug 12, 2021 | AITU | A | CASE ASSIGNED TO INTENT TO USE PARALEGAL | Loading... |
Aug 3, 2021 | IUCN | S | NOTICE OF ALLOWANCE CANCELLED | Loading... |
Aug 3, 2021 | D1BR | I | TEAS DELETE 1(B) BASIS RECEIVED | Loading... |
Jul 27, 2021 | NOAM | E | NOA E-MAILED - SOU REQUIRED FROM APPLICANT | Loading... |
Jun 1, 2021 | NPUB | E | OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED | Loading... |
Jun 1, 2021 | PUBO | A | PUBLISHED FOR OPPOSITION | Loading... |
May 12, 2021 | NONP | E | NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED | Loading... |
Apr 23, 2021 | CNSA | P | APPROVED FOR PUB - PRINCIPAL REGISTER | Loading... |
Apr 22, 2021 | TEME | I | TEAS/EMAIL CORRESPONDENCE ENTERED | Loading... |
Apr 22, 2021 | CRFA | I | CORRESPONDENCE RECEIVED IN LAW OFFICE | Loading... |
Apr 22, 2021 | ERFR | I | TEAS REQUEST FOR RECONSIDERATION RECEIVED | Loading... |
Apr 20, 2021 | GNFN | O | NOTIFICATION OF FINAL REFUSAL EMAILED | Loading... |
Apr 20, 2021 | GNFR | O | FINAL REFUSAL E-MAILED | Loading... |
Apr 20, 2021 | CNFR | R | FINAL REFUSAL WRITTEN | Loading... |
Mar 29, 2021 | PARI | I | TEAS VOLUNTARY AMENDMENT RECEIVED | Loading... |
Mar 29, 2021 | AMPX | O | PRELIMINARY/VOLUNTARY AMENDMENT - ENTERED | Loading... |
Mar 9, 2021 | TEME | I | TEAS/EMAIL CORRESPONDENCE ENTERED | Loading... |
Mar 9, 2021 | CRFA | I | CORRESPONDENCE RECEIVED IN LAW OFFICE | Loading... |
Mar 3, 2021 | TROA | I | TEAS RESPONSE TO OFFICE ACTION RECEIVED | Loading... |
Dec 22, 2020 | GNRN | O | NOTIFICATION OF NON-FINAL ACTION E-MAILED | Loading... |
Dec 22, 2020 | GNRT | F | NON-FINAL ACTION E-MAILED | Loading... |
Dec 22, 2020 | CNRT | R | NON-FINAL ACTION WRITTEN | Loading... |
Dec 21, 2020 | DOCK | D | ASSIGNED TO EXAMINER | Loading... |
Dec 2, 2020 | AMPX | O | PRELIMINARY/VOLUNTARY AMENDMENT - ENTERED | Loading... |
Nov 30, 2020 | ALIE | A | ASSIGNED TO LIE | Loading... |
Sep 25, 2020 | NWOS | I | NEW APPLICATION OFFICE SUPPLIED DATA ENTERED | Loading... |
Sep 14, 2020 | PARI | I | TEAS VOLUNTARY AMENDMENT RECEIVED | Loading... |
Aug 27, 2020 | NWAP | I | NEW APPLICATION ENTERED | Loading... |
Detailed Classifications
Class 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
Class 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
Class 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
Additional Information
Pseudo Mark
FOR MEDIC MEDICS RISE
Classification
International Classes
035
041
042