VALGENESIS IOPS

Live / Allowed — Published for opposition (as of 17 Feb 2026)

What this means for you

Approved and waiting on proof of use. It will register unless the applicant drops it, and its 01 Apr 2025 filing date already counts against anyone who files later.

Record

Serial number
99115166
Mark type
Stylized text
Filed
01 Apr 2025
Published for opposition
17 Feb 2026
Attorney of record
Thomas E. Watson

Goods and services

  • Class 009 — Scientific and electric apparatus: Downloadable web-based database software using artificial intelligence for data analytics for improving the operational efficiency of the paperless validation of an inventory tracking system; Downloadable cloud-based software using artificial intelligence for data analytics for improving the operational efficiency of the paperless validation of an inventory tracking system; Downloadable enterprise software for data analytics for improving the operational efficiency of the paperless validation of an inventory tracking system; Downloadable mobile applications for data analytics for improving the operational efficiency of the paperless validation of an inventory tracking system; Downloadable application software for data analytics for improving the operational efficiency of the paperless validation of an inventory tracking system; Recorded computer firmware for data analytics for improving the operational efficiency of the paperless validation of an inventory tracking system; Downloadable server-based software platform for data analytics for improving the operational efficiency of the paperless validation of an inventory tracking system
  • Class 042 — Scientific and technological services: 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) featuring computer software platforms using artificial intelligence for paperless validation of software 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 managing 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 managing equipment for automated testing of inventory tracking systems, and for analyzing risk management data; Providing temporary use of non-downloadable web-based database software used for the 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 managing equipment for automated testing of inventory tracking systems, and for analyzing risk management data; Providing temporary use of on-line non-downloadable cloud-based 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 managing equipment for automated testing of inventory tracking systems, 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 managing equipment for automated testing of inventory tracking systems, 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, for performing quality control operations, for temperature measurement, for maintaining logs of equipment, for measuring critical quality and process control, for calibrating critical quality and process control parameters, for document management, for enterprise resource management, for laboratory information management, for managing equipment for automated testing of inventory tracking systems, and for analyzing risk management data

Owner

Prior registrations

Prosecution history

  • 17 Feb 2026 — OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED
  • 17 Feb 2026 — PUBLISHED FOR OPPOSITION
  • 11 Feb 2026 — NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED
  • 23 Jan 2026 — APPROVED FOR PUB - PRINCIPAL REGISTER
  • 23 Jan 2026 — EXAMINER'S AMENDMENT ENTERED
  • 23 Jan 2026 — NOTIFICATION OF EXAMINERS AMENDMENT E-MAILED
  • 23 Jan 2026 — EXAMINERS AMENDMENT E-MAILED
  • 23 Jan 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
  • 29 Aug 2025 — NOTIFICATION OF NON-FINAL ACTION E-MAILED

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