VAL
Live / Allowed — Published for opposition (as of 03 Mar 2026)
What this means for you
Approved and waiting on proof of use. It will register unless the applicant drops it, and its 10 Jun 2025 filing date already counts against anyone who files later.
Record
- Serial number
- 99226889
- Mark type
- Stylized text
- Filed
- 10 Jun 2025
- Published for opposition
- 03 Mar 2026
- Attorney of record
- Thomas E. Watson
Goods and services
- Class 009 — Scientific and electric apparatus: Downloadable cloud-based software using artificial intelligence for analyzing and improving the operational efficiency of validating an inventory tracking system; Downloadable web-based database software using artificial intelligence for analyzing and improving the operational efficiency of validating an inventory tracking system; Downloadable enterprise software for analyzing and improving the operational efficiency of validating an inventory tracking system; Downloadable mobile applications for analyzing and improving the operational efficiency of validating an inventory tracking system; Downloadable application software for analyzing and improving the operational efficiency of validating an inventory tracking system; Recorded computer firmware for analyzing and improving the operational efficiency of validating an inventory tracking system; Downloadable server-based software platform for analyzing and improving the operational efficiency of validating an inventory tracking system; Downloadable chatbot software for replying to questions from online customers related to an inventory tracking system, and for providing step-by-step guidance via chatbot interface regarding the automated creation and execution of documents for regulatory compliance and adherence to internal processes; Downloadable software for generating validation documentation for equipment, software, and process qualification featuring automated content generation, specification-based updates, and content quality enhancement; Downloadable software for executing validation procedures by parsing user-uploaded evidence, comparing actual and expected results, and automatically updating result records in real time; Downloadable software for automated analysis and verification of user-uploaded evidence in testing workflows featuring evidence parsing, comparison with expected results and test steps, and detection of anomalies or mismatches; Downloadable chatbot software for paperless validation of software, equipment and processes required by life sciences companies in order to meet the regulatory requirement of life sciences regulators, for remote inspection of pharmaceuticals during manufacture, for performing quality control operations, for temperature measurement, for maintaining logs of logging equipment, for measuring critical quality and process control parameters use in metrology operations, for calibrating equipment used in the manufacture of medical devices and biopharmaceutical products, for document management, for enterprise resource management, for laboratory information management, for performing automated tests, and for analyzing risk management data
- Class 042 — Scientific and technological services: Providing temporary use of non-downloadable chatbot software for replying to questions from online customers related to an inventory tracking system, and for providing step-by-step guidance via chatbot interface regarding the automated creation and execution of documents for regulatory compliance and adherence to internal processes; Providing online non-downloadable chatbot software for paperless validation of software, equipment and processes required by life sciences companies in order to meet the regulatory requirement of life sciences regulators, for remote inspection of pharmaceuticals during manufacturing operations, for performing quality control operations, for temperature measurement, for logging equipment, for measuring critical quality and process control parameters in metrology operations, for calibrating equipment used in the manufacture of medical devices and biopharmaceutical products, for document management, for enterprise resource management, for laboratory information management, and for automated testing of pharmaceuticals; Software as a service (SaaS) services featuring software for automated generation of validation protocols for equipment, software, and process qualification featuring dynamically updating content based on specifications for improving documentation quality; Software as a service (SaaS) services featuring software for automated execution of validation protocols, featuring evidence parsing, result comparison, and real-time population of actual results; Software as a service (SaaS) services featuring software for automated detection of anomalies in test executions by parsing user-uploaded images, comparing results against expected outcomes, and verifying attached evidence; Consultation and advisory services in the field of computer software regarding software implementation; Consultancy in the field of artificial intelligence technology; Platform as a service (PaaS) services featuring computer software platforms using artificial intelligence for paperless validation of test results and for automating document creation and execution, for evidence processing for regulatory compliance and adherence to internal processes, for remote inspection of pharmaceuticals during manufacture, for performing quality control operations, for temperature measurement, for maintaining logs of equipment, for measuring critical quality and process control parameters, for calibrating equipment used in the manufacture of medical devices and biopharmaceutical products, for document management, for enterprise resource management, for laboratory information management, for managing manufacturing equipment, for automated testing of inventory tracking systems, and for analyzing risk management data; Software as a service (SaaS) services featuring software using artificial intelligence for paperless validation of software used to automate document creation and execution, for evidence processing for regulatory compliance and adherence to internal processes, for remote inspection of pharmaceuticals during manufacture, for performing quality control operations, for temperature measurement, for maintaining logs of equipment, for measuring critical quality and process control parameters, for calibrating equipment used in the manufacture of medical devices and biopharmaceutical products, for document management, for enterprise resource management, for laboratory information management, for performing automated tests, and for analyzing risk management data; Providing temporary use of non-downloadable web-based database software for qualification and paperless validation of an inventory tracking system; Providing temporary use of non-downloadable computer software using artificial intelligence for paperless validation of software used to automate document creation and execution, for evidence processing for regulatory compliance and adherence to internal processes, for remote inspection of pharmaceuticals during manufacture, for performing quality control operations, for temperature measurement, for maintaining logs of equipment, for measuring critical quality and process control parameters, for calibrating equipment used in the manufacture of medical devices and biopharmaceutical products, for document management, for enterprise resource management, for laboratory information management, for performing automated tests, and for analyzing risk management data; Providing temporary use of on-line non-downloadable cloud-based software using artificial intelligence for use in paperless validation of software used to automate document creation and execution, for evidence processing for regulatory compliance and adherence to internal processes, for remote inspection of pharmaceuticals during manufacture, for performing quality control operations, for temperature measurement, for maintaining logs of equipment, for measuring critical quality and process control parameters, for calibrating critical quality and process control parameters, for document management, for enterprise resource management, for laboratory information management, for performing automated tests, and for analyzing risk management data; Providing temporary use of online, non-downloadable enterprise software using artificial intelligence for paperless validation of software, equipment and processes required by life sciences companies in order to meet the regulatory requirement of life sciences regulators, for remote inspection of pharmaceuticals during manufacture, for performing quality control operations, for temperature measurement, for maintaining logs of equipment, for measuring critical quality and process control parameters, for calibrating equipment used in the manufacture of medical devices and biopharmaceutical products, for document management, for enterprise resource management, for laboratory information management, for performing automated tests, and for analyzing risk management data; Providing a website featuring temporary use of non- downloadable software using artificial intelligence for paperless validation of software, equipment and processes required by life sciences companies in order to meet the regulatory requirement of life sciences regulators, for remote inspection of pharmaceuticals during manufacture, for performing quality control operations, for temperature measurement, for maintaining logs of equipment, for measuring critical quality and process control parameters, for calibrating equipment used in the manufacture of medical devices and biopharmaceutical products, for document management, for enterprise resource management, for laboratory information management, for performing automated tests, and for analyzing risk management data
Owner
- ValGenesis, Inc., Santa Clara, CA, US
- ValGenesis, Inc., Santa Clara, CA, US
Prosecution history
- 03 Mar 2026 — OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED
- 03 Mar 2026 — PUBLISHED FOR OPPOSITION
- 25 Feb 2026 — NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED
- 04 Feb 2026 — APPROVED FOR PUB - PRINCIPAL REGISTER
- 04 Feb 2026 — EXAMINER'S AMENDMENT ENTERED
- 04 Feb 2026 — NOTIFICATION OF EXAMINERS AMENDMENT E-MAILED
- 04 Feb 2026 — EXAMINERS AMENDMENT E-MAILED
- 04 Feb 2026 — EXAMINERS AMENDMENT -WRITTEN
- 29 Dec 2025 — NOTIFICATION OF FINAL REFUSAL EMAILED
- 29 Dec 2025 — FINAL REFUSAL E-MAILED
- 29 Dec 2025 — FINAL REFUSAL WRITTEN
- 26 Nov 2025 — TEAS/EMAIL CORRESPONDENCE ENTERED
- 26 Nov 2025 — CORRESPONDENCE RECEIVED IN LAW OFFICE
- 26 Nov 2025 — TEAS RESPONSE TO OFFICE ACTION RECEIVED
- 30 Aug 2025 — NOTIFICATION OF NON-FINAL ACTION E-MAILED