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Brands and Their Owners
| Brand | Owner (click to sort) | Address | Description |
|---|---|---|---|
| I3 | RAVEN HOLDCO | 500 ATRIUM DRIVE SOMERSET NJ 08873 | Training clinical trial site personnel in the use of tests and rating systems for drug protocol requirements; and training clinical trial site personnel in the use of medical and research equipment required by drug protocols;The mark consists of a lower case letter i and numeral 3 in white text within a red square.;I THREE; INGENIX THREE;The color(s) red and white is/are claimed as a feature of the mark.; |
| I3 RESEARCH | RAVEN HOLDCO | 500 ATRIUM DRIVE SOMERSET NJ 08873 | Training clinical trial site personnel in the use of tests and rating systems for drug protocol requirements; and training clinical trial site personnel in the use of medical and research equipment required by drug protocols;I-THREE RESEARCH;Management services of a business nature for clinical trials in the field of investigational drugs, namely, arranging for sites to perform clinical trials, arranging for the import, packaging, shipping, labeling and distribution of drugs and other investigational supplies to and from the clinical trial sites, arranging for the central collection of laboratory specimens from clinical trial sites, making any and all filings required by the Food and Drug Administration for investigational new drugs, preparing statistical reports resulting from clinical trials;RESEARCH;Management services of a scientific and technical nature for clinical trials in the field of investigational drugs, namely, conducting clinical protocols and trials for others; consulting services regarding scientific and technical aspects of clinical trials of investigational drugs, namely, advising others on conducting clinical protocols and trials and the regulatory requirements of the Food and Drug administration; technical writing for others of clinical report forms which are required by clinical trial drug protocols; technical writing for others of clinical trial reports; database development services to process data collected from clinical trials; |
| INGENIX PHARMACEUTICAL SERVICES | INGENIX, INC. | 13625 Technology Drive Eden Prairie MN 55344 | Training Clinical Trial Site Personnel in the Use of Tests and Rating Systems for Drug Protocol Requirements; and Training Clinical Trial Site Personnel in the Use of Medical and Research Equipment Required by Drug Protocols;Management Services of a Business Nature for Clinical Trials in the Field of Investigational Drugs, Namely, Arranging for Sites to Perform Clinical Trials, Arranging for the Import, Packaging, Shipping, Labeling and Distribution of Drugs and Other Investigational Supplies to and from the Clinical Trial Sites, Arranging for the Central Collection of Laboratory Specimens from Clinical Trial Sites, Making Any and All Filings Required by the Food and Drug Administration for Investigational New Drugs, Preparing Statistical Reports Resulting from Clinical Trials;PHARMACEUTICAL SERVICES;Management Services of a Scientific and Technical Nature for Clinical Trials in the Field of Investigational Drugs, Namely, Conducting Clinical Protocols and Trials for Others; Consulting Services Regarding Scientific and Technical Aspects of Clinical Trials of Investigational Drugs, Namely, Advising Others on Conducting Clinical Protocols and Trials and the Regulatory Requirements of the Food And Drug Administration; Technical Writing for Others of Clinical Report Forms Which Are Required by Clinical Trial Drug Protocols; Technical Writing for Others of Clinical Trial Reports; Database Development Services to Process Data Collected from Clinical Trials; |
| INTEGREX | Integrated Research | 505 S. Main Street, Suite 950 Orange CA 92868 | TRAINING CLINICAL TRIAL SITE PERSONNEL CONCERNING DRUG PROTOCOL REQUIREMENTS AND THE USE OF TESTS AND RATING SYSTEMS FOR SUCH PROTOCOL; TRAINING CLINICAL TRIAL PERSONNEL IN THE USE OF MEDICAL AND RESEARCH EQUIPMENT REQUIRED BY DRUG AND/OR DEVICE PROTOCOLS; ARRANGING MEDICAL CONFERENCES AND SYMPOSIA; PROVIDING CONTINUING MEDICAL EDUCATION TO PHYSICIANS AND OTHER HEALTH-CARE PROVIDERS AND ARRANGING AND MANAGING SPEAKERS' BUREAUS IN CONJUNCTION THEREWITH; MEDICAL MANUSCRIPT PREPARATION AND SUBMISSION; DEVELOPMENT AND PUBLICATION OF MEDICAL JOURNALS;MANAGEMENT ASSISTANCE FOR CLINICAL TRIALS OF INVESTIGATIONAL DRUGS, NAMELY, ARRANGING FOR SITES TO PERFORM CLINICAL TRIALS, ARRANGING FOR THE IMPORT, PACKAGING, SHIPPING, LABELING, AND DISTRIBUTION OF DRUGS AND OTHER INVESTIGATIONAL SUPPLIES AND EQUIPMENT TO AND FROM THE CLINICAL TRIAL SITES, ARRANGING FOR THE CENTRAL COLLECTION OF LABORATORY SPECIMENS FROM CLINICAL TRIAL SITES, MAKING ANY AND ALL FILINGS REQUIRED BY THE FOOD AND DRUG ADMINISTRATION FOR INVESTIGATIONAL NEW DRUGS AND NEW DRUG APPLICATIONS, PREPARING STATISTICAL REPORTS RESULTING FROM CLINICAL TRIALS; COOPERATIVE ADVERTISING AND MARKETING OF NEW DRUGS;PROVIDING MEDICAL MONITORING SERVICES, NAMELY REVIEW OF TRAIL DATA REPORTS FOR SAFETY PURPOSES, AND TO DETERMINE AND ASSURE COMPLIANCE WITH CLINICAL STUDY PROTOCOL REQUIREMENTS AS WELL AS COMPLIANCE WITH GOOD CLINICAL PRACTICES AND FOOD AND DRUG ADMINISTRATION AND/OR OTHER REGULATIONS GOVERNING CLINICAL TRIALS;TECHNICAL WRITING OF CLINICAL TRIAL REPORTS FOR OTHERS; DATABASE DEVELOPMENT SERVICES TO PROCESS DATA COLLECTED FROM CLINICAL TRIALS; PHARMACEUTICAL DRUG DEVELOPMENT SERVICES; |
| INTEGRIUM | Integrated Research | 505 S. Main Street, Suite 950 Orange CA 92868 | TRAINING CLINICAL TRIAL SITE PERSONNEL CONCERNING DRUG PROTOCOL REQUIREMENTS AND THE USE OF TESTS AND RATING SYSTEMS FOR SUCH PROTOCOL; TRAINING CLINICAL TRIAL PERSONNEL IN THE USE OF MEDICAL AND RESEARCH EQUIPMENT REQUIRED BY DRUG AND/OR DEVICE PROTOCOLS; ARRANGING MEDICAL CONFERENCES AND SYMPOSIA; PROVIDING CONTINUING MEDICAL EDUCATION TO PHYSICIANS AND OTHER HEALTH-CARE PROVIDERS AND ARRANGING AND MANAGING SPEAKERS' BUREAUS IN CONJUNCTION THEREWITH; MEDICAL MANUSCRIPT PREPARATION AND SUBMISSION; DEVELOPMENT AND PUBLICATION OF MEDICAL JOURNALS;REAL ESTATE SITE SELECTION, NAMELY, INSPECTING BUILDINGS AND OFFICES AS POTENTIAL SITES FOR HOSTING CLINICAL TRIALS;MANAGEMENT ASSISTANCE FOR CLINICAL TRIALS OF INVESTIGATIONAL DRUGS, NAMELY, ARRANGING FOR SITES TO PERFORM CLINICAL TRIALS, ARRANGING FOR THE IMPORT, PACKAGING, SHIPPING, LABELING, AND DISTRIBUTION OF DRUGS AND OTHER INVESTIGATIONAL SUPPLIES AND EQUIPMENT TO AND FROM THE CLINICAL TRIAL SITES, ARRANGING FOR THE CENTRAL COLLECTION OF LABORATORY SPECIMENS FROM CLINICAL TRIAL SITES, MAKING ANY AND ALL FILINGS REQUIRED BY THE FOOD AND DRUG ADMINISTRATION FOR INVESTIGATIONAL NEW DRUGS AND NEW DRUG APPLICATIONS, PREPARING STATISTICAL REPORTS RESULTING FROM CLINICAL TRIALS; COOPERATIVE ADVERTISING AND MARKETING OF NEW DRUGS;PROVIDING MEDICAL MONITORING SERVICES, NAMELY, REVIEW OF TRAIL DATA REPORTS FOR SAFETY PURPOSES, AND TO DETERMINE AND ASSURE COMPLIANCE WITH CLINICAL STUDY PROTOCOL REQUIREMENTS AS WELL AS COMPLIANCE WITH GOOD CLINICAL PRACTICES AND FOOD AND DRUG ADMINISTRATION AND/OR OTHER REGULATIONS GOVERNING CLINICAL TRIALS;TECHNICAL WRITING OF CLINICAL TRIAL REPORTS FOR OTHERS; DATABASE DEVELOPMENT SERVICES TO PROCESS DATA COLLECTED FROM CLINICAL TRIALS; PHARMACEUTICAL DRUG DEVELOPMENT SERVICES; |
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| INTEGRIUM | Integrium | 14351 Myford Road Tustin CA 92780 | TRAINING CLINICAL TRIAL SITE PERSONNEL CONCERNING DRUG PROTOCOL REQUIREMENTS AND THE USE OF TESTS AND RATING SYSTEMS FOR SUCH PROTOCOL; TRAINING CLINICAL TRIAL PERSONNEL IN THE USE OF MEDICAL AND RESEARCH EQUIPMENT REQUIRED BY DRUG AND/OR DEVICE PROTOCOLS; ARRANGING MEDICAL CONFERENCES AND SYMPOSIA; PROVIDING CONTINUING MEDICAL EDUCATION TO PHYSICIANS AND OTHER HEALTH-CARE PROVIDERS AND ARRANGING AND MANAGING SPEAKERS' BUREAUS IN CONJUNCTION THEREWITH; MEDICAL MANUSCRIPT PREPARATION AND SUBMISSION; DEVELOPMENT AND PUBLICATION OF MEDICAL JOURNALS;REAL ESTATE SITE SELECTION, NAMELY, INSPECTING BUILDINGS AND OFFICES AS POTENTIAL SITES FOR HOSTING CLINICAL TRIALS;MANAGEMENT ASSISTANCE FOR CLINICAL TRIALS OF INVESTIGATIONAL DRUGS, NAMELY, ARRANGING FOR SITES TO PERFORM CLINICAL TRIALS, ARRANGING FOR THE IMPORT, PACKAGING, SHIPPING, LABELING, AND DISTRIBUTION OF DRUGS AND OTHER INVESTIGATIONAL SUPPLIES AND EQUIPMENT TO AND FROM THE CLINICAL TRIAL SITES, ARRANGING FOR THE CENTRAL COLLECTION OF LABORATORY SPECIMENS FROM CLINICAL TRIAL SITES, MAKING ANY AND ALL FILINGS REQUIRED BY THE FOOD AND DRUG ADMINISTRATION FOR INVESTIGATIONAL NEW DRUGS AND NEW DRUG APPLICATIONS, PREPARING STATISTICAL REPORTS RESULTING FROM CLINICAL TRIALS; COOPERATIVE ADVERTISING AND MARKETING OF NEW DRUGS;PROVIDING MEDICAL MONITORING SERVICES, NAMELY REVIEW OF TRIAL DATA REPORTS FOR SAFETY PURPOSES, AND TO DETERMINE AND ASSURE COMPLIANCE WITH CLINICAL STUDY PROTOCOL REQUIREMENTS AS WELL AS COMPLIANCE WITH GOOD CLINICAL PRACTICES AND FOOD AND DRUG ADMINISTRATION AND/OR OTHER REGULATIONS GOVERNING CLINICAL TRIALS;TECHNICAL WRITING OF CLINICAL TRIAL REPORTS FOR OTHERS; DATABASE DEVELOPMENT SERVICES TO PROCESS DATA COLLECTED FROM CLINICAL TRIALS; PHARMACEUTICAL DRUG DEVELOPMENT SERVICES; |
| OPTUMINSIGHT | OPTUM, INC. | Legal Intake 9900 Bren Road East Minnetonka MN 55343 | Training clinical trial site personnel in the use of tests and rating systems for drug protocol requirements; training clinical trial site personnel in the use of medical and research equipment required by drug protocols; educational services, namely, providing clinical education training to physicians and hospital managed care personnel in the fields of utilization review, case management, medical cost management, and quality assurance;OPTUMIN SIGHT; |
| TEXAS CLINICAL TRIALS | WCT HOLDINGS | 767 FIFTH AVENUE, 48TH FLOOR NEW YORK NY 10153 | Training clinical trial site personnel concerning drug protocol requirements and the use of tests and rating systems for such protocol; training clinical trial site personnel in the use of medical and research equipment required by drug protocols;Building inspection, namely, inspecting potential sites for hosting clinical trials;Management assistance and consultation for clinical trials of investigational drugs, namely, arranging for sites to perform clinical trials, arranging for the import, packaging, shipping, labeling, and distribution of drugs and other investigational supplies to and from the clinical trial sites, arranging for the central collection of laboratory specimens from clinical trial sites, making any and all filings required by the food and drug administration for investigational new drugs, preparing statistical reports resulting from clinical trials;Technical writing of clinical report forms which are required by clinical trial drug protocols; technical writing of clinical trial reports; database development services to process data collected from clinical trials; |
| WCT | WORLDWIDE CLINICAL TRIALS, INC. | 401 North Maple Drive Beverly Hills CA 90210 | TRAINING CLINICAL TRIAL SITE PERSONNEL CONCERNING DRUG PROTOCOL REQUIREMENTS AND THE USE OF TESTS AND RATING SYSTEMS FOR SUCH PROTOCOL; TRAINING CLINICAL TRIAL SITE PERSONNEL IN THE USE OF MEDICAL AND RESEARCH EQUIPMENT REQUIRED BY DRUG PROTOCOLS;BUILDING INSPECTION, NAMELY, INSPECTING POTENTIAL SITES FOR HOSTING CLINICAL TRIALS;MANAGEMENT ASSISTANCE AND CONSULTATION FOR CLINICAL TRIALS OF INVESTIGATIONAL DRUGS, NAMELY, ARRANGING FOR SITES TO PERFORM CLINICAL TRIALS, ARRANGING FOR THE IMPORT, PACKAGING, SHIPPING, LABELING, AND DISTRIBUTION OF DRUGS AND OTHER INVESTIGATIONAL SUPPLIES TO AND FROM THE CLINICAL TRIAL SITES, ARRANGING FOR THE CENTRAL COLLECTION OF LABORATORY SPECIMENS FROM CLINICAL TRIAL SITES, MAKING ANY AND ALL FILINGS REQUIRED BY THE FOOD AND DRUG ADMINISTRATION FOR INVESTIGATIONAL NEW DRUGS, PREPARING STATISTICAL REPORTS RESULTING FROM CLINICAL TRIALS;the representation of the design of a medical caduceus symbol;TECHNICAL WRITING OF CLINICAL REPORT FORMS WHICH ARE REQUIRED BY CLINICAL TRIAL DRUG PROTOCOLS; TECHNICAL WRITING OF CLINICAL TRIAL REPORTS; DATABASE DEVELOPMENT SERVICES TO PROCESS DATA COLLECTED FROM CLINICAL TRIALS; |
| WCT | WORLDWIDE CLINICAL TRIALS, INC. | 401 North Maple Drive Beverly Hills CA 90210 | Training clinical trial site personnel concerning drug protocol requirements and the use of tests and rating systems for such protocol; training clinical trial site personnel in the use of medical and research equipment required by drug protocols;Real estate site selection, namely, inspecting potential sites for hosting clinical trials;WORLDWIDE CLINICAL TRIALS;Color is not claimed as a feature of the mark.;Business management assistance and consultation for clinical trials of investigational drugs, namely, arranging for sites to perform clinical trials, arranging for the import, packaging, shipping, labeling, and distribution of drugs and other investigational supplies to and from the clinical trial sites, arranging for the central collection of laboratory specimens from clinical trial sites, making any and all filings required by the food and drug administration for investigational new drugs, preparing statistical reports resulting from clinical trials;Technical writing of clinical report forms for others which are required by clinical trial drug protocols; technical writing of clinical trial reports for others; database development services to process data collected from clinical trials; |
| WCT | WORLDWIDE CLINICAL TRIALS, INC. | 401 North Maple Drive Beverly Hills CA 90210 | Training clinical trial site personnel concerning drug protocol requirements and the use of tests and rating systems for such protocol; training clinical trial site personnel in the use of medical and research equipment required by drug protocols;Real estate site selection, namely, inspecting potential sites for hosting clinical trials;WORLDWIDE CLINICAL TRIALS;Business management assistance and consultation for clinical trials of investigational drugs, namely, arranging for sites to perform clinical trials, arranging for the import, packaging, shipping, labeling, and distribution of drugs and other investigational supplies to and from the clinical trial sites, arranging for the central collection of laboratory specimens from clinical trial sites, making any and all filings required by the food and drug administration for investigational new drugs, preparing statistical reports resulting from clinical trials;Technical writing of clinical report forms for others which are required by clinical trial drug protocols; technical writing of clinical trial reports for others; database development services to process data collected from clinical trials; |
| WCT WORLDWIDE CLINICAL TRIALS | WORLDWIDE CLINICAL TRIALS, INC. | 401 North Maple Drive Beverly Hills CA 90210 | Training clinical trial site personnel concerning drug protocol requirements and the use of tests and rating systems for such protocol; training clinical trial site personnel in the use of medical and research equipment required by drug protocols;Real estate site selection, namely, inspecting potential sites for hosting clinical trials;Business management assistance and consultation for clinical trials of investigational drugs, namely, arranging for sites to perform clinical trials, arranging for the import, packaging, shipping, labeling, and distribution of drugs and other investigational supplies to and from the clinical trial sites, arranging for the central collection of laboratory specimens from clinical trial sites, making any and all filings required by the food and drug administration for investigational new drugs, preparing statistical reports resulting from clinical trials;WORLDWIDE CLINICAL TRIALS;Technical writing of clinical report forms for others which are required by clinical trial drug protocols; technical writing of clinical trial reports for others; database development services to process data collected from clinical trials; |
| WORLDWIDE CLINICAL TRIALS | WORLDWIDE CLINICAL TRIALS, INC. | 401 North Maple Drive Beverly Hills CA 90210 | training clinical trial site personnel concerning drug protocol requirements and the use of tests and rating systems for such protocol; training clinical trial site personnel in the use of medical and research equipment required by drug protocols;building inspection, namely, inspecting potential sites for hosting clinical trials;WORLD WIDE CLINICAL TRIALS;as to WORLDWIDE CLINICAL TRIALS;management assistance and consultation for clinical trials of investigational drugs, namely, arranging for sites to perform clinical trials, arranging for the import, packaging, shipping, labeling, and distribution of drugs and other investigational supplies to and from the clinical trial sites, arranging for the central collection of laboratory specimens from clinical trial sites, making any and all filings required by the food and drug administration for investigational new drugs, preparing statistical reports resulting from clinical trials;CLINICAL TRIALS and the design of the caduceus symbol;technical writing of clinical report forms which are required by clinical trial drug protocols; technical writing of clinical trial reports; database development services to process data collected from clinical trials; |
| WORLDWIDE CLINICAL TRIALS | WORLDWIDE CLINICAL TRIALS, INC. | 401 North Maple Drive Beverly Hills CA 90210 | Training clinical trial site personnel concerning drug protocol requirements and the use of tests and rating systems for such protocol; training clinical trial site personnel in the use of medical and research equipment required by drug protocols;The mark consists of the image of a globe bisected with the image of a caduceus above the words WORLDWIDE CLINICAL TRIALS.;The drawing is amended to appear as follows: Publish New Cut, the mark consists of the image of a globe with the image of a caduceus above the words Worldwide Clinical Trials, is inserted.;Real estate site selection, namely, inspecting potential sites for hosting clinical trials;WORLD WIDE CLINICAL TRIALS;Color is not claimed as a feature of the mark.;Business management assistance and consultation for clinical trials of investigational drugs, namely, arranging for sites to perform clinical trials, arranging for the import, packaging, shipping, labeling, and distribution of drugs and other investigational supplies to and from the clinical trial sites, arranging for the central collection of laboratory specimens from clinical trial sites, making any and all filings required by the food and drug administration for investigational new drugs, preparing statistical reports resulting from clinical trials;WORLDWIDE CLINICAL TRIALS;Technical writing of clinical report forms for others which are required by clinical trial drug protocols; technical writing of clinical trial reports for others; database development services to process data collected from clinical trials; |
| WORLDWIDE CLINICAL TRIALS | WORLDWIDE CLINICAL TRIALS | 767 FIFTH AVENUE, 48TH FLOOR NEW YORK NY 10153 | Training clinical trial site personnel concerning drug protocol requirements and the use of tests and rating systems for such protocol; training clinical trial site personnel in the use of medical and research equipment required by drug protocols;The mark consists of the image of a globe bisected with the image of a caduceus above the words WORLDWIDE CLINICAL TRIALS.;The drawing is amended to appear as follows: Publish New Cut, the mark consists of the image of a globe with the image of a caduceus above the words Worldwide Clinical Trials, is inserted.;Real estate site selection, namely, inspecting potential sites for hosting clinical trials;WORLD WIDE CLINICAL TRIALS;Color is not claimed as a feature of the mark.;Business management assistance and consultation for clinical trials of investigational drugs, namely, arranging for sites to perform clinical trials, arranging for the import, packaging, shipping, labeling, and distribution of drugs and other investigational supplies to and from the clinical trial sites, arranging for the central collection of laboratory specimens from clinical trial sites, making any and all filings required by the food and drug administration for investigational new drugs, preparing statistical reports resulting from clinical trials;WORLDWIDE CLINICAL TRIALS;Technical writing of clinical report forms for others which are required by clinical trial drug protocols; technical writing of clinical trial reports for others; database development services to process data collected from clinical trials; |
| WORLDWIDE CLINICAL TRIALS | Maple Leaf Ventures | 401 North Maple Drive Beverly Hills CA 90210 | Training clinical trial site personnel concerning drug protocol requirements and the use of tests and rating systems for such protocol; training clinical trial site personnel in the use of medical and research equipment required by drug protocols;The mark consists of the image of a globe bisected with the image of a caduceus above the words WORLDWIDE CLINICAL TRIALS.;The drawing is amended to appear as follows: Publish New Cut, the mark consists of the image of a globe with the image of a caduceus above the words Worldwide Clinical Trials, is inserted.;Real estate site selection, namely, inspecting potential sites for hosting clinical trials;WORLD WIDE CLINICAL TRIALS;Color is not claimed as a feature of the mark.;Business management assistance and consultation for clinical trials of investigational drugs, namely, arranging for sites to perform clinical trials, arranging for the import, packaging, shipping, labeling, and distribution of drugs and other investigational supplies to and from the clinical trial sites, arranging for the central collection of laboratory specimens from clinical trial sites, making any and all filings required by the food and drug administration for investigational new drugs, preparing statistical reports resulting from clinical trials;WORLDWIDE CLINICAL TRIALS;Technical writing of clinical report forms for others which are required by clinical trial drug protocols; technical writing of clinical trial reports for others; database development services to process data collected from clinical trials; |
| WORLDWIDE EVIDENCE | WORLDWIDE CLINICAL TRIALS, INC. | 401 North Maple Drive Beverly Hills CA 90210 | Training clinical trial site personnel concerning protocol requirements and the use of tests and rating systems for such protocol; training clinical trial site personnel in the use of medical and research equipment and procedures required by protocols;Business consulting and management in the field of clinical trials; Pharmaceutical cost management services and drug utilization review services; Business management assistance and consultation for clinical trials of observational research designs, namely, management and compilation of information in the field of clinical trials for business purposes, namely, surveys, retrospective chart review, prospective longitudinal cohort studies, post approval safety studies (pass), registries, and interventional studies for approved and investigational drugs; Business management services, namely, arranging for sites to perform clinical trials, arranging for the import, packaging, shipping labeling, and distribution of drugs and other investigational supplies to and from the clinical trial sites as appropriate to the study design, arranging for the central collection of laboratory specimens from clinical trial sites, extracting data from clinical trial records including electronic healthcare records, making any and all filings required by the food and drug administration as well as the EMA for observational research, and as appropriate investigational new drugs, preparing statistical reports resulting from clinical trials an studies, all for business purposes;Pharmaceutical research services; Pharmaceutical research and development; Technical writing of clinical report forms for others which are required by clinical trial study protocols; Technical writing of clinical trial reports for others; Database development services to process data collected from clinical trials; |
Where the owner name is not linked, that owner no longer owns the brand |
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