GleanMark

TARGET HEALTH Trademark

TARGET HEALTH is a USPTO trademark filed by TARGET HEALTH, LLC. Status: Registered.

Trademark Facts

MarkTARGET HEALTH
Serial Number78313401
Registration Number3156025
StatusRegistered
Filing Date2003-10-14
Registration Date2006-10-17
Mark TypeWord
Nice Classes035 (Advertising & Business), 041 (Education & Entertainment), 042 (Software & IT), 044 (Medical Services)
OwnerTARGET HEALTH, LLC
Attorney of RecordKenneth I. Kohn
Prosecution Events28
Latest EventREM2 on 2025-10-17

Goods & Services

Class 035: Business auditing services, namely, performing pre-inspection goods manufacturing practices audits and assuring that user fee monies are submitted; biostatistics and data processing services; providing statistical information; performing statistical analyses; manufacturer representatives in the field of pharmaceuticals; Class 041: Computer services, namely, providing online journals in fields of health and medicine; Class 042: Providing quality assurance services in the field of pharmaceuticals; reviewing standards and practices to assure compliance with medical and pharmaceutical laws and regulations; reviewing standards and practices to assure compliance with US Food and Drug Administration (FDA) laws and regulations; consulting services regarding food and drug law and regulation compliance, namely, preparing for and conducting meetings to discuss and negotiate development strategies, preparing and submitting documents and forms required by the FDA, preparing responses to FDA questions and warning letters, follow-up with FDA on post application submission questions, preparing for and conducting meetings with legal counsel, troubleshooting product and process issues, performing analytical methods development and validation, and designing and implementing safety and regulatory toxicology programs; intellectual property licensing in the fields of drug, drug product, pharmaceutical and pharmaceutical products; medical and scientific research, namely, conducting clinical trials, specifically preparing protocols, case report forms and informed consent forms, performing qualification, initiation, monitoring and closeout visits, generating investigator study files, monitor drug supply, identifying study sites and managing investigator payments, and preparing clinical sites for FDA inspection; consultation in the fields of drug development, including working with sponsor, medical, scientific, toxicology, manufacturing and business experts to clearly delineate development requirements, evaluating available and competitive technologies; product and process development services; technical writing for others, specifically, integrated clinical and statistical study reports and other regulatory manuscripts; Class 044: Providing an on-line database for use in gathering and providing patient records and patient data via a global computer network

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