Legal Representation
Attorney
Carrie Webb Olson
USPTO Deadlines
Next Deadline
820 days remaining
Section 8 (6-Year) Declaration Due (Based on registration date 2021-10-26)
Due Date
October 26, 2027
Grace Period Ends
April 26, 2028
Additional deadlines exist. Contact your attorney for complete deadline information.
Application History
32 eventsDate | Code | Type | Description | Documents |
---|---|---|---|---|
May 7, 2025 | CHAN | I | APPLICANT/CORRESPONDENCE CHANGES (NON-RESPONSIVE) ENTERED | Loading... |
May 7, 2025 | COAR | I | TEAS CHANGE OF OWNER ADDRESS RECEIVED | Loading... |
May 7, 2025 | EWAF | I | TEAS WITHDRAWAL OF ATTORNEY RECEIVED-FIRM RETAINS | Loading... |
May 7, 2025 | ARAA | I | ATTORNEY/DOM.REP.REVOKED AND/OR APPOINTED | 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 | TCCA | I | TEAS CHANGE OF CORRESPONDENCE RECEIVED | Loading... |
Oct 26, 2021 | R.PR | A | REGISTERED-PRINCIPAL REGISTER | Loading... |
Aug 10, 2021 | NPUB | E | OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED | Loading... |
Aug 10, 2021 | PUBO | A | PUBLISHED FOR OPPOSITION | Loading... |
Jul 21, 2021 | NONP | E | NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED | Loading... |
Jul 1, 2021 | CNSA | O | APPROVED FOR PUB - PRINCIPAL REGISTER | Loading... |
Jul 1, 2021 | XAEC | I | EXAMINER'S AMENDMENT ENTERED | Loading... |
Jul 1, 2021 | GNEN | O | NOTIFICATION OF EXAMINERS AMENDMENT E-MAILED | Loading... |
Jul 1, 2021 | GNEA | O | EXAMINERS AMENDMENT E-MAILED | Loading... |
Jul 1, 2021 | CNEA | R | EXAMINERS AMENDMENT -WRITTEN | Loading... |
Jun 21, 2021 | TEME | I | TEAS/EMAIL CORRESPONDENCE ENTERED | Loading... |
Jun 21, 2021 | CRFA | I | CORRESPONDENCE RECEIVED IN LAW OFFICE | Loading... |
Jun 17, 2021 | ALIE | A | ASSIGNED TO LIE | Loading... |
Mar 29, 2021 | ERSI | I | TEAS RESPONSE TO SUSPENSION INQUIRY RECEIVED | Loading... |
Mar 25, 2021 | GNS3 | O | NOTIFICATION OF LETTER OF SUSPENSION E-MAILED | Loading... |
Mar 25, 2021 | GNSL | S | LETTER OF SUSPENSION E-MAILED | Loading... |
Mar 25, 2021 | CNSL | R | SUSPENSION LETTER WRITTEN | Loading... |
Mar 4, 2021 | TEME | I | TEAS/EMAIL CORRESPONDENCE ENTERED | Loading... |
Mar 3, 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... |
Oct 8, 2020 | NWOS | I | NEW APPLICATION OFFICE SUPPLIED DATA ENTERED | Loading... |
Sep 7, 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
Classification
International Classes
035
041
042