USPTO serial 99542861
VEEVA
Reviewed by CopyMark Law Group
Status 661
- Filing date
- Status date
- Registration date
- —
- Examiner
- BURKE, KELLY CHRISTINE
- Law office
- TMO LAW OFFICE 128
What this means
This page summarizes the public USPTO record for this serial number, including owners, goods and services, and prosecution history.
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Owner
Pleasanton, CA, US
Attorney of record
The USPTO lists this attorney as the applicant's representative for correspondence on this application.
David A.W. Wong
David A.W. Wong Barnes & Thornburg LLP11 South Meridian StreetIndianapolis, IN 46204-3535United StatesGoods and services
| Class | Description | Status | First use |
|---|---|---|---|
| 009 | Downloadable computer software, recorded computer software, and downloadable mobile applications for document management in the field of life sciences, pharmaceutical, biotechnology, medical device, and consumer products industries; Downloadable computer software, recorded computer software, and downloadable mobile applications featuring artificial intelligence (AI), generative artificial intelligence, machine learning, predictive analytics, data analytics, and intelligent software agents (bots) for use in customer relationship management (CRM), patient relationship management, sales force automation and effectiveness, marketing automation, managing, planning, and executing customer engagement, omnichannel communications, and live, virtual, and hybrid events; Downloadable computer software, recorded computer software, and downloadable mobile applications for clinical operations and clinical trial management, namely, managing, tracking, and organizing clinical trials, study startup, electronic trial master files (eTMF), site activation, randomization and trial supply management, clinical trial disclosures, and clinical trial payments; Downloadable computer software, recorded computer software, and downloadable mobile applications for clinical data management, namely, electronic data capture (EDC), building and managing clinical studies, aggregating, cleaning, and transforming clinical data from multiple sources, and capturing patient data, electronic clinical outcome assessments (eCOA), and patient-reported outcomes; Downloadable computer software, recorded computer software, and downloadable mobile applications for regulatory affairs and regulatory information management (RIM), namely, managing, planning, tracking, and reporting on product registrations, submissions, health authority interactions, regulatory content, and submissions archives; Downloadable computer software, recorded computer software, and downloadable mobile applications for quality management (QMS), namely, managing quality processes, GxP documents, compliant content, validation, validation management, and compliance training, logging, creating, viewing, searching, and submitting quality events, nonconformance reports (NCRs), and incidents, and capturing and adding photographic and visual evidence to quality records; Downloadable computer software, recorded computer software, and downloadable mobile applications for pharmacovigilance and drug safety, namely, adverse event management, managing safety content, safety signal detection and management, and advanced reporting and analysis, management of commercial, medical, and promotional content, including creation, review, approval, distribution, and digital asset management (DAM) of compliant promotional and medical materials, master data management (MDM) of customer, product, and reference data, territory and sales roster planning and alignment, digital engagement and omnichannel communications between life sciences company representatives and healthcare professionals, scheduling and conducting remote meetings and video calls, secure and compliant chat and messaging, sharing, viewing, and receiving approved promotional and medical content and patient resources, and for requesting samples and capturing electronic signatures remotely; Downloadable computer software, recorded computer software, and downloadable mobile applications for performing internal and external audits, namely, for downloading, accessing, completing, and submitting audit checklists authored in a central database, capturing and recording audit findings, observations, and comments, and for attaching supporting evidence, including photos, videos, and files, to audit records; Downloadable and recorded software development tools; Downloadable searchable electronic files and databases for use with computer software, featuring medical, scientific, and commercial data for scientific and medical research purposes, namely, data regarding clinical trials, medical research, healthcare providers (HCPs), healthcare organizations (HCOs), key opinion leaders (KOLs), and anonymized longitudinal patient data (APLD); Downloadable and recorded computer software and mobile application software for the access, management, organization, collaboration, and sharing of content, communications, electronic data, and information in the fields of customer relationship management (CRM), content management, and life sciences clinical trial document collection, management, and analysis; Downloadable and recorded computer software and mobile application software for the collection, editing, managing, organizing, modifying, bookmarking, transmission storage and sharing of data and information; Downloadable and recorded computer software and mobile application software for the collection, editing, managing, organizing, modifying, bookmarking, transmission storage and sharing of clinical data and information; Downloadable and recorded computer software and mobile application software for providing users the ability to create, modify, edit, share, manage, store, and view electronic media or information over the Internet or other communications network; Downloadable and recorded computer software and mobile application software for use in customer relationship management (CRM); Downloadable and recorded computer software and mobile application software for maintaining document control; Downloadable and recorded computer software and mobile application software for document management and content management; Downloadable and recorded computer software and mobile application quality management software; Downloadable and recorded computer software and mobile application software for performing quality control management of business operations; Downloadable and recorded computer software and mobile application software for users to create, edit, manage, store, retrieve, access, track, profile, categorize, search, publish, archive, deliver, administer, modify and control files, text, images, electronic content, data, and clinical data; Downloadable and recorded computer software and mobile application software for data management; Downloadable and recorded computer software and mobile application software for clinical data management; Downloadable software development kits (SDK); Downloadable computer software and mobile application software for use in the creation, development, operation and testing of software applications; all of the foregoing for the purposes of providing solutions for the management of clinical trial documents, regulatory documents and filings and submissions, quality management documentation and claims management documentation, and claims management documentation, and for the purposes of providing solutions for customer relationship management ("CRM") | ACTIVE | Mar 1, 2011 |
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 |
|---|---|---|---|
| Aug 6, 2026 | TEME | TEAS/EMAIL CORRESPONDENCE ENTERED | — |
| Aug 5, 2026 | CRFA | CORRESPONDENCE RECEIVED IN LAW OFFICE | — |
| Aug 5, 2026 | TROA | TEAS RESPONSE TO OFFICE ACTION RECEIVED | This event means the applicant filed a response to a USPTO Office Action — typically arguments, amendments, or evidence addressing the examiner's objections. The USPTO will review the response and either allow the mark to proceed or issue another action. |
| May 8, 2026 | GNRN | NOTIFICATION OF NON-FINAL ACTION E-MAILED | A non-final Office Action means the USPTO examining attorney has raised at least one issue with your trademark application but has not made a final decision. You usually have three months to respond with arguments, amendments, or evidence. Missing the deadline can abandon the application. |
| May 8, 2026 | GNRT | NON-FINAL ACTION E-MAILED | A non-final Office Action means the USPTO examining attorney has raised at least one issue with your trademark application but has not made a final decision. You usually have three months to respond with arguments, amendments, or evidence. Missing the deadline can abandon the application. |
| May 8, 2026 | CNRT | NON-FINAL ACTION WRITTEN | A non-final Office Action means the USPTO examining attorney has raised at least one issue with your trademark application but has not made a final decision. You usually have three months to respond with arguments, amendments, or evidence. Missing the deadline can abandon the application. |
| Apr 15, 2026 | DOCK | ASSIGNED TO EXAMINER | — |
| Dec 12, 2025 | NWOS | NEW APPLICATION OFFICE SUPPLIED DATA ENTERED | — |
| Dec 11, 2025 | MAFR | APPLICATION FILING RECEIPT MAILED | — |
| Dec 11, 2025 | NWAP | NEW APPLICATION ENTERED | — |