Drawing for PATIENTS FIRST. POWERED BY EVIDENCE.

USPTO serial 98288528

PATIENTS FIRST. POWERED BY EVIDENCE.

Reviewed by CopyMark Law Group

Status 654
Filing date
Status date
Registration date
—
Examiner
ORDOGNE, ROBERT J
Law office
TMO LAW OFFICE 126

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

Attorney of record

The USPTO lists this attorney as the applicant's representative for correspondence on this application.

Lisa Casey Spaniel

Lisa Casey Spaniel BLANK ROME LLPONE LOGAN SQUARE8TH FLOORPHILADELPHIA, PA 19103

Goods and services

ClassDescriptionStatusFirst use
009downloadable computer software, computer software platforms, and mobile applications featuring digital assets and artificial intelligence for database management, analytics, modeling, monitoring, storage, validation, compliance, reimbursement management, scheduling, progress monitoring, benefits verification, reimbursements and case management in the field of Clinical Research, Safety Services, Risk Evaluation and Mitigation, Patient Support Services, Evidence Development and Data AnalysisACTIVE—
016printed materials, namely, brochures, manuals and handbooks featuring topics relating to health, medical and pharmaceutical education, training and testing in connection with patient assistance programs for the pharmaceutical and healthcare industriesACTIVE—
035consulting services in the cost management of health care, namely, cost management for the health care benefit plans of others, including health care benefit plans that have co-pay cards; medical cost management and administering medication reimbursement programs for others to improve health, affordability and patient experience; business consulting services featuring business analytics and information in the healthcare and pharmaceutical industries during drug development and commercialization, namely, business analytics and information in the fields of real world evidence, health economics, outcomes research, payer research and market access studies; strategic business data analysis and business advice regarding benefit cost management, pharmaceutical end-user behavior and healthcare use behavior; business consulting services in the fields of business risk minimization, business risk mitigation and business Risk Evaluation and Mitigation Strategies; business management of in-home care coordination services, business organization and management of a nationwide home health network, business organization and management of a nationwide injection network; business administration services, namely, customer relationship management services design and implementation of customer services solutions via various technology partnerships and custom configurations connecting vendors and services and hybrid operating platform designs and deployments; Business administration of co-pay programs for reimbursement of co-pays and access to medication discounts, benefit verification, claims administration and other support for reimbursement and access to benefitsACTIVE—
036Consulting services in the payment management of health care, namely, co-pay cards, therapeutic access, reimbursement, analysis of manufacturer program designs and medication discount benefitsACTIVE—
038webcasting services featuring topics in the field of health, medical care and pharmaceutical industriesACTIVE—
041educational, training and educational testing services, namely, conducting seminars, conferences and presentations featuring topics in the field of health, medical care and pharmaceutical industries; training and educational services, namely, conducting programs in the fields of health, medical care and pharmaceutical industries; training and educational services, namely, providing non-downloadable webcasts in the fields of health, medical care and pharmaceutical industriesACTIVE—
042medical and scientific research, namely, conducting clinical trials for others; basic and clinical research in the field of heath care and medicine; providing on-line non-downloadable software, computer software platforms, and applications featuring artificial intelligence and digital assets used to administer, advise, monitor, analyze or generate information related to Clinical Research, Safety Services, Risk Evaluation and Mitigation, Patient Support Services, Evidence Development and Data Analysis; non-downloadable software as a service (SAAS) technology platforms for database management, analytics, modeling, monitoring, storage, validation, compliance, payment management, scheduling, progress monitoring, benefits verification, reimbursements and cost management related to Clinical Research, Safety Services, Risk Evaluation and Mitigation, Patient Support Services, Evidence Development and Data Analysis; providing on-line non-downloadable software, platforms, and mobile applications featuring digital assets and artificial intelligence for database management, analytics, modeling, monitoring, storage, validation, compliance, payment management, scheduling, progress monitoring, benefits verification, reimbursements and cost management in the field of clinical research, safety services, risk evaluation and mitigation, patient support services, evidence development and data analysis; scientific research consulting services in the field of pharmacovigilance strategies to ensure regulatory compliance and patient safety in clinical trials and marketed pharmaceuticals involving human subjects; scientific research consulting services in the field of epidemiology; pharmaceutical product safety testing and consultancy efficacy services for the purposes of, namely, risk mitigation and pharmacovigilance services, prescription drug monitoring programs, analyzing clinical data in healthcare databases, clinical trials, health economics and outcomes research in the fields of healthcare and pharmaceuticals, organizing, managing, and tracking data during development of a clinical trial, creating and updating clinical guidelines in the fields of healthcare and pharmaceuticalsACTIVE—
044healthcare services in the nature of remote and in-person patient support services, namely, nursing services, dose administration in the nature of patient engagement to ensure adherence to dosing protocols, and patient medical diagnostic monitoring servicesACTIVE—
045consultation services in the field of research compliance, namely, regulatory compliance consultation services in the field of clinical trials involving human subjects; regulatory compliance consultation services in the field of informed consent protocols for clinical trial participants, Pregnancy registries, Pregnancy Root cause analysis, Risk Evaluation and Mitigation Strategy administration, Observational Research Real world Evidence, Real world Data, Knowledge Attitude and Behavior Surveys, Proprietary Risk Evaluation and Mitigation Strategy Platform, Expanded Patient Access Programs, Clinical Trial and Post Marketing Case Processing, Post Marketing Commitments, Post Marketing Requirements, Risk Minimization Plans, Risk Evaluation and Mitigation, Patient HUB, Benefit Investigation, Interventional Clinical Trials, Natural History Studies, Pragmatic Studies Design and Administration of Outcomes Based Agreements and value based agreements, Federated Registries, Integrated Registries, Decentralized Studies, and Patient Recruitment StrategiesACTIVE—

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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

DateCodeEventWhat it means
Aug 9, 2026RCSCREPORT COMPLETED SUSPENSION CHECK CASE STILL SUSPENDED—
Feb 9, 2026GNS3NOTIFICATION OF LETTER OF SUSPENSION E-MAILED—
Feb 9, 2026GNSLLETTER OF SUSPENSION E-MAILED—
Feb 9, 2026CNSLSUSPENSION LETTER WRITTEN—
Oct 7, 2025TEMETEAS/EMAIL CORRESPONDENCE ENTERED—
Oct 7, 2025CRFACORRESPONDENCE RECEIVED IN LAW OFFICE—
Oct 7, 2025TROATEAS RESPONSE TO OFFICE ACTION RECEIVEDThis 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.
Jul 7, 2025XELGAPPLICATION EXTENSION GRANTED/RECEIPT PROVIDED—
Jul 7, 2025XELRAPPLICATION EXTENSION TO RESPONSE PERIOD - RECEIVED—
Apr 7, 2025GNRNNOTIFICATION OF NON-FINAL ACTION E-MAILEDA 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 7, 2025GNRTNON-FINAL ACTION E-MAILEDA 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 7, 2025CNRTNON-FINAL ACTION WRITTENA 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.
Feb 4, 2025DOCKASSIGNED TO EXAMINER—
Jan 10, 2025DOCKASSIGNED TO EXAMINER—
Dec 29, 2024TEMETEAS/EMAIL CORRESPONDENCE ENTERED—
Dec 29, 2024CRFACORRESPONDENCE RECEIVED IN LAW OFFICE—
Dec 29, 2024TROATEAS RESPONSE TO OFFICE ACTION RECEIVEDThis 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.
Sep 30, 2024XELGAPPLICATION EXTENSION GRANTED/RECEIPT PROVIDED—
Sep 30, 2024XELRAPPLICATION EXTENSION TO RESPONSE PERIOD - RECEIVED—
Jun 29, 2024GNRNNOTIFICATION OF NON-FINAL ACTION E-MAILEDA 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.
Jun 29, 2024GNRTNON-FINAL ACTION E-MAILEDA 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.
Jun 29, 2024CNRTNON-FINAL ACTION WRITTENA 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.
Jun 29, 2024LOPELETTER OF PROTEST EVIDENCE REVIEWED - ACTION TAKEN—
Jun 26, 2024DOCKASSIGNED TO EXAMINER—
Mar 18, 2024LOPTLETTER OF PROTEST EVIDENCE FORWARDED—
Jan 22, 2024NWOSNEW APPLICATION OFFICE SUPPLIED DATA ENTERED—
Dec 1, 2023NWAPNEW APPLICATION ENTERED—

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