USPTO serial 99622625
SMARTSOLVE
Reviewed by CopyMark Law Group
- Filing date
- Status date
- Registration date
- —
- Examiner
- HARRELL, CHARITY MAJETTE
- Law office
- FILE REPOSITORY (FRANCONIA)
What this means
Status 686 means your mark is published in the USPTO Official Gazette and in the 30-day opposition period. If no opposition is filed, prosecution typically continues toward registration or a Notice of Allowance. Monitor the opposition window. After it closes, watch for Notice of Allowance (intent-to-use) or registration (use-based).
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Owner
PARSIPPANY, NJ, US
PARSIPPANY, NJ, US
PARSIPPANY, NJ, US
Attorney of record
The USPTO lists this attorney as the applicant's representative for correspondence on this application.
Cynthia Johnson Walden
Cynthia Johnson Walden Fish & Richardson P.C.P.O. Box 1022Minneapolis, MN 55440-1022United StatesGoods and services
| Class | Description | Status | First use |
|---|---|---|---|
| 042 | Providing on-line non-downloadable software for enterprise quality management; Providing on-line non-downloadable software for regulatory compliance and quality management tracking, managing, auditing, and reporting in the pharmaceutical, MedTech, healthcare, medical, life sciences, regulatory, quality management and compliance industries; Providing on-line non-downloadable software for analysis, quality control, quality audit management, quality change and deviation management, quality design control, quality event management, quality CAPA management, quality risk management, and quality design control, in the pharmaceutical, MedTech, healthcare, medical, life sciences, regulatory, quality management and compliance industries; Providing on-line non-downloadable software for regulatory information management, regulatory submissions and publishing, regulator health authority interactions and regulatory lifecycle management in the pharmaceutical, MedTech, healthcare, medical, life sciences, regulatory, quality management and compliance industries; Providing on-line non-downloadable software for managing data and business processes for quality and compliance in the field of enterprise quality management and enterprise regulatory information management; Providing on-line non-downloadable software for document management, risk management, supplier management, project management, task and issue tracking, and communication and collaboration; Providing on-line non-downloadable software for processing, tracking, managing, reviewing, and reporting complaints and adverse events in the pharmaceutical, MedTech, healthcare, medical, life sciences, regulatory, quality management and compliance industries; Providing on-line non-downloadable software for training management in the in the pharmaceutical, MedTech, healthcare, medical, life sciences, regulatory, quality management and compliance industries; Providing on-line non-downloadable software for planning, managing, conducting, and reporting on quality and regulatory audits in the pharmaceutical, MedTech, healthcare, medical, and life sciences industries; Providing on-line non-downloadable software for asset management, supply management, and supplier management in the pharmaceutical, MedTech, healthcare, medical, and life sciences industries; Software as a service (SAAS) services featuring software for enterprise quality management; Software as a service (SAAS) services featuring software for enterprise regulatory information management; Software as a service (SAAS) services featuring software for regulatory compliance and quality management tracking, managing, auditing, and reporting in the pharmaceutical, MedTech, healthcare, medical, life sciences, regulatory, quality management and compliance industries; Software as a service (SAAS) services featuring software for analysis, quality control, quality audit management, quality change and deviation management, quality design control, quality event management, quality CAPA management, quality risk management, and quality design control, in the pharmaceutical, MedTech, healthcare, medical, life sciences, regulatory, quality management and compliance industries; Software as a service (SAAS) services featuring software for regulatory information management, regulatory submissions and publishing, regulator health authority interactions and regulatory lifecycle management in the pharmaceutical, MedTech, healthcare, medical, life sciences, regulatory, quality management and compliance industries; Software as a service (SAAS) services featuring software for managing data and business processes for quality and compliance in the field of enterprise quality management and enterprise regulatory information management; Software as a service (SAAS) services featuring software for document management, risk management, supplier management, project management, task and issue tracking, and communication and collaboration; Software as a service (SAAS) services featuring software for processing, tracking, managing, reviewing, and reporting complaints and adverse events in the pharmaceutical, MedTech, healthcare, medical, life sciences, regulatory, quality management and compliance industries; Software as a service (SAAS) services featuring software for training management in the in the pharmaceutical, MedTech, healthcare, medical, life sciences, regulatory, quality management and compliance industries; Software as a service (SAAS) services featuring software for planning, managing, conducting, and reporting on quality and regulatory audits in the pharmaceutical, MedTech, healthcare, medical, and life sciences industries; Software as a service (SAAS) services featuring software for asset management, supply management, and supplier management in the pharmaceutical, MedTech, healthcare, medical, and life sciences industries; Software as a service (SAAS) services featuring software for accessing, searching, creating, editing, modifying, collaborating, categorizing, controlling, storing, and managing; Software as a service (SAAS) services featuring software for validating, retrieving, archiving, delivering, analyzing, tracking, managing, auditing, and reporting data, documents, and images in the fields of quality assurance and management, quality control, manufacturing quality, regulatory compliance, regulatory information management, submission management, registration management, process automation, supplier management, customer experience, non-conformance deviation, and corrective and preventative action management; Providing on-line non-downloadable software for enterprise regulatory information management; Providing on-line non-downloadable software for accessing, searching, creating, editing, modifying, collaborating, categorizing, controlling, storing, and managing; Providing on-line non-downloadable software for validating, retrieving, archiving, delivering, analyzing, tracking, managing, auditing, and reporting data, documents, and images in the fields of quality assurance and management, quality control, manufacturing quality, regulatory compliance, regulatory information management, submission management, registration management, process automation, supplier management, customer experience, non-conformance deviation, and corrective and preventative action management | ACTIVE | Feb 12, 2003 |
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.
Prosecution history
| Date | Code | Event | What it means |
|---|---|---|---|
| Sep 8, 2026 | NRCC | NOTICE OF REGISTRATION CONFIRMATION EMAILED | — |
| Sep 8, 2026 | 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. |
| Jul 21, 2026 | NPUB | OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED | — |
| Jul 21, 2026 | 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 15, 2026 | NONP | NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED | — |
| Jun 24, 2026 | CNSA | APPROVED FOR PUB - PRINCIPAL REGISTER | — |
| May 27, 2026 | DOCK | ASSIGNED TO EXAMINER | — |
| May 22, 2026 | NWOS | NEW APPLICATION OFFICE SUPPLIED DATA ENTERED | — |
| Jan 29, 2026 | MAFR | APPLICATION FILING RECEIPT MAILED | — |
| Jan 29, 2026 | NWAP | NEW APPLICATION ENTERED | — |