TARGET HEALTH, LLC

TARGET DOCUMENT

Provision of access to data or documents stored electronically in central files for remote consultation;Document;

TARGET E*CRF

IN THE STATEMENT, COLUMN 2, THE MARK CONSISTS OF STANDARD CHARACTERS WITHOUT CLAIM TO ANY PARTICULAR FONT, STYLE, SIZE, OR COLOR IS INSERTED, AND THE DRAWING IS AMENDED TO APPEAR AS FOLLOWS : Target e*CRF;ECRF;providing an online database for use in gathering and providing clinical trial data;

TARGET E*CTR

TARGET E * CENTER; TARGET ELECTRONIC * CENTER;Data processing services; Providing statistical information for business or commercial purposes; Business auditing services; data processing services in the biostatistics field; Performing statistical analysis for business purposes; Manufacturer representatives in the field of pharmaceuticals; development of business processes for the analysis and implementation of clinical trials dealing with pharmaceutical drug development;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; legal consulting services regarding Food and Drug law and regulation compliance, namely, consulting in the preparation of legal negotiations, in the preparation of legal documents and forms required by the FDA, in the preparation of responses to FDA questions and warning letters, and the follow-up with FDA on post application submission questions, in the preparation of meetings with legal counsel; intellectual property licensing in the fields of drug, drug product, pharmaceutical and pharmaceutical products;Providing online computer database for use in gathering and providing clinical trial data regarding medical and scientific research; Scientific research; Product research and development; medical and scientific research services in the field of treatment and diagnosis provided for medical service providers; Technical writing for others; Providing quality assurance services in the field of pharmaceuticals; medical and scientific research featuring troubleshooting product and process development problems dealing with safety and regulatory toxicology programs in the field of pharmaceutical drugs; Medical and scientific research, namely, conducting clinical trials; Consultation in the fields of pharmaceutical drug development and conducting clinical trials; consultation in the fields of pharmaceutical drug development, namely, consulting with sponsor, medical, scientific, toxicology, manufacturing and business experts to clearly delineate development requirements and evaluate available and competitive technologies; Product development processes; Technical writing for others, namely, writing integrated clinical and statistical study reports and other regulatory manuscripts; compiling data in the nature of patient records via a global computer information network for research purposes in the field of medical science and medical consultancy;

TARGET E*ICF

Downloadable electronic data files featuring informed consent forms submitted for compliance with FDA legal requirements for product review in the fields of product safety, product advertising and product promotion standards;Printed informed consent form submitted for compliance with FDA legal requirements for product review in the fields of product safety, product advertising and product promotion standards;E-ICF;

TARGET E*STUDIO

Providing a website featuring non-downloadable software for use in gathering and providing clinical trial data regarding medical and scientific research; Scientific research; Technical consultation and research in the medical and pharmaceutical fields; Product research and development; medical and scientific research services in the field of treatment and diagnosis provided for medical service providers; Technical writing for others; Providing quality assurance services in the field of pharmaceuticals; troubleshooting of product and process development problems dealing with safety and regulatory toxicology programs as it relates to medical and scientific research in the development of pharmaceutical drugs; Medical and scientific research, namely, conducting clinical trials; Consultation in the fields of pharmaceutical drug development, conducting clinical trials; consultation in the field of pharmaceuticals drug development, namely, consulting with sponsor, medical, scientific, toxicology, manufacturing and business experts to clearly delineate development requirements and evaluate available and competitive technologies; development of pharmaceutical product processes for others; Technical writing for others, namely, writing integrated clinical and statistical study reports and regulatory manuscripts relating to medical and scientific research in the development of pharmaceutical drugs, as an integrated component; compiling patient records and patient data via a global computer information network for research purposes in the fields of medical science and medical consultancy;

TARGET ENCODER

Computer software used to code medications and adverse events;ENCODER;

TARGET HEALTH

Computer services, namely, providing online journals in fields of health and medicine;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;Providing an on-line database for use in gathering and providing patient records and patient data via a global computer network;HEALTH;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;

TARGET HEALTH INC

The mark consists of the words Target Health Inc in black, above the word Health from the e'' to the h is the upper half of a red and white target, from the T in Target to the e in Health is a curved arrow with the black tail of the arrow starting at the T and the head of the arrow which is red in color ending at the e, the body of the arrow is concave and widening from the tail to the head, on the target is the caduceus symbol in black and white.;The color(s) red, black, and white is/are claimed as a feature of the mark.;Data processing; Providing statistical information for business or commercial purposes; Business auditing services; data processing services in the biostatistics field; Performing statistical analysis for business or commercial purposes; manufacturer representatives in the field of pharmaceuticals; development of business processes for the analysis and implementation of clinical trials dealing with pharmaceutical drug development;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; legal consulting services regarding Food and Drug law and regulation compliance, namely, consulting in the preparation of legal negotiations, in the preparation of legal documents and forms required by the FDA, in the preparation of responses to FDA questions and warning letters, and the follow-up with FDA on post application submission questions, in the preparation of meetings with legal counsel; intellectual property licensing in the fields of drug, drug product, pharmaceutical and pharmaceutical products;HEALTH INC.;Providing online computer database for use in gathering and providing clinical trials data regarding medical and scientific research; Scientific research; Research in the medical and pharmaceutical fields; Product research and development; medical and scientific research services in the field of treatment and diagnosis provided for medical service providers; Technical writing for others; Providing quality assurance services in the field of pharmaceuticals; troubleshooting of product and process development problems dealing with safety and regulatory toxicology programs as it relates to medical and scientific research in the development of pharmaceutical drugs; Medical and scientific research, namely, conducting clinical trials; Consultation in the fields of pharmaceutical drug development, namely, conducting clinical trials; consultation in the fields of pharmaceutical drug development, namely, consulting with sponsor, medical, scientific, toxicology, manufacturing and business experts to clearly delineate development requirements and evaluate available and competitive technologies; Development of pharmaceutical product processes for others; Technical writing for others, namely, writing integrated clinical and statistical study reports and regulatory manuscripts related to medical and scientific research in the development of pharmaceutical drugs, as an integrated component; compiling patient records and patient data via a global computer information network for research purposes in the field of medical science and medical consultancy;