SMARTSOLVE

What this means for you

Approved and waiting on proof of use. It will register unless the applicant drops it, and its 29 Jan 2026 filing date already counts against anyone who files later.

Record

Serial number

99622625

Mark type

Stylized text

Filed

29 Jan 2026

Published for opposition

21 Jul 2026

Attorney of record

Cynthia Johnson Walden

Goods and services

• Class 042 — Scientific and technological services: 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

Owner

• IQVIA Inc., PARSIPPANY, NJ, US
• IQVIA Inc., PARSIPPANY, NJ, US

Prosecution history

• 08 Sept 2026 — NOTICE OF REGISTRATION CONFIRMATION EMAILED
• 08 Sept 2026 — REGISTERED-PRINCIPAL REGISTER
• 21 Jul 2026 — OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED
• 21 Jul 2026 — PUBLISHED FOR OPPOSITION
• 15 Jul 2026 — NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED
• 24 Jun 2026 — APPROVED FOR PUB - PRINCIPAL REGISTER
• 27 May 2026 — ASSIGNED TO EXAMINER
• 22 May 2026 — NEW APPLICATION OFFICE SUPPLIED DATA ENTERED
• 29 Jan 2026 — APPLICATION FILING RECEIPT MAILED
• 29 Jan 2026 — NEW APPLICATION ENTERED