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Brands and Their Owners
| Brand | Owner (click to sort) | Address | Description |
|---|---|---|---|
| ADVANTAGE IRB | THE EMMES COMPANY | 401 North Washington Street, Suite 700 Rockville MD 20850 | Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research;IRB; |
| ADVARRA | ADVARRA, INC. | 6100 Merriweather Drive, Suite 600 Columbia MD 21044 | Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research; providing information relating to regulatory compliance for independent review of clinical trials involving human subjects; |
| ADVARRA | Chesapeake Research Review | Suite 110 6940 Columbia Gateway Drive Columbia MD 21046 | Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research; providing information relating to regulatory compliance for independent review of clinical trials involving human subjects; |
| APTIVINSITE | APTIV SOLUTIONS | 1925 ISAAC NEWTON SQUARE SUITE 100 RESTON VA 20190 | providing independent review of clinical trials for business purposes;providing medical and scientific research information in the field of clinical trials; providing review and monitoring of medical and scientific research data in clinical trials; |
| ASPIRE IRB | WESTERN INSTITUTIONAL REVIEW BOARD, INC. | 1019 39TH AVENUE SE SUITE 120 PUYALLUP WA 98374 | Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research;IRB; |
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| ASPIRE IRB | ASPIRE INDEPENDENT REVIEW BOARD, INC. | 202 CARNEGIE CENTER, SUITE 107 PRINCETON NJ 08540 | Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research;IRB; |
| ASPIRE IRB | Aspire IRB | 11491 Woodside Avenue Santee CA 92071 | Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research;IRB; |
| CANCER INSIGHT | Cancer Insight | 1305 East Houston Street San Antonio TX 78205 | Providing independent review of clinical trials for business purposes; Business consulting and management in the field of clinical trials, namely, providing information management services; Business consulting and management in the field of clinical trials, namely, management and compilation of computerized databases in the field of clinical trials for business purposes; Business consulting and management in the field of clinical trials, namely, clinical data and regulatory submission management on behalf of medical, biopharmaceutical and biotechnology companies to assist them with clinical research, clinical trials and applications for drug approval; Providing consulting services in the field of regulatory submission management to medical companies to assist them with applications for medical device approval; Regulatory submission management, namely, assisting others in preparing and filing applications for new drugs with governmental regulatory bodies; Providing business intelligence services in the fields of medical devices and pharmaceuticals;Regulatory compliance consulting in the field of medical products; Regulatory compliance consulting in the field of prescription drug sampling;CANCER;Medical and scientific research, namely, conducting clinical trials for others; Conducting clinical trials for others; Providing medical and scientific research information in the field of clinical trials; Providing medical and scientific research information in the field of pharmaceuticals and clinical trials; Conducting research and clinical trials for others relating to medical devices and pharmaceuticals; Consulting services for others in the field of design, planning, and implementation project management of scientific research and clinical trials; Medical research; Scientific research and development; Biomedical research services; Providing information about medical and scientific research; Research and development of vaccines and medicines; Consulting services in the fields of biotechnology and pharmaceutical research and development; Pharmaceutical research and development; Pharmaceutical drug development services; Technical research in the field of pharmaceutical studies; Conducting early evaluations in the field of new pharmaceuticals; Development of pharmaceutical preparations and medicines; |
| CLINICAL RESEARCH INSIGHT | Clinical Research Insight | 1305 East Houston Street San Antonio TX 78205 | Providing independent review of clinical trials for business purposes; Business consulting and management in the field of clinical trials, namely, providing information management services; Business consulting and management in the field of clinical trials, namely, management and compilation of computerized databases in the field of clinical trials for business purposes; Business consulting and management in the field of clinical trials, namely, clinical data and regulatory submission management on behalf of medical, biopharmaceutical and biotechnology companies to assist them with clinical research, clinical trials and applications for drug approval; Providing consulting services in the field of regulatory submission management to medical companies to assist them with applications for medical device approval; Regulatory submission management, namely, assisting others in preparing and filing applications for new drugs with governmental regulatory bodies; Providing business intelligence services in the fields of medical devices and pharmaceuticals;Regulatory compliance consulting in the field of medical products; Regulatory compliance consulting in the field of prescription drug sampling;Medical and scientific research, namely, conducting clinical trials for others; Conducting clinical trials for others; Providing medical and scientific research information in the field of clinical trials; Providing medical and scientific research information in the field of pharmaceuticals and clinical trials; Conducting research and clinical trials for others relating to medical devices and pharmaceuticals; Consulting services for others in the field of design, planning, and implementation project management of scientific research and clinical trials; Medical research; Scientific research and development; Biomedical research services; Providing information about medical and scientific research; Research and development of vaccines and medicines; Consulting services in the fields of biotechnology and pharmaceutical research and development; Pharmaceutical research and development; Pharmaceutical drug development services; Technical research in the field of pharmaceutical studies; Conducting early evaluations in the field of new pharmaceuticals; Development of pharmaceutical preparations and medicines; |
| COMPASS IRB | CHESAPEAKE RESEARCH REVIEW | 6940 Columbia Gateway Drive, Suite 110 Columbia MD 21046 | Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols to ensure protection of the rights and welfare of human subjects of research;IRB; |
| CQC CONTINUOUS QUALITY CONTROL | MedAvante Inc. | 100 American Metro Blvd #106 Hamilton NJ 08619 | Providing independent review of clinical trials for business purposes; |
| EMANCIPATION MONTH | Dewitt Lee | 34 Brinton St Buffalo NY 14214 | Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research; |
| EXCELLENCE. EVERY TIME. | CHESAPEAKE RESEARCH REVIEW | 6940 Columbia Gateway Drive, Suite 110 Columbia MD 21046 | Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research; providing information on independent review of clinical trials involving human subjects; |
| EXPERIENCE AND INNOVATION IN ETHICAL REVIEW | The Copernicus Group, Inc. | Post Office Box 110605 Research Triangle Park NC 27709 | Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research;Providing an on-line database featuring healthcare research information;Providing a web site for use by others to manage and exchange healthcare research information; providing use of nondownloadable computer software via the internet for managing healthcare research and support information; |
| GUIDING YOU TO SUCCESS | CHESAPEAKE RESEARCH REVIEW | 6940 Columbia Gateway Drive, Suite 110 Columbia MD 21046 | Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols to ensure protection of the rights and welfare of human subjects of research; |
| ICEMAN TRIAL | Kiromic, Inc. | Trish Faulkner 7707 Fannin Street, Suite 140 Houston TX 78257 | Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research; |
| LET OUR PEOPLE GO | GREEN, ARON | 8 FL 30 WALL ST NYC NY 10005 | Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research; Providing information in the field of human rights relating to religious Jews in Israel; |
| LUMABRIDGE | LUMABRIDGE | 1305 EAST HOUSTON STREET SAN ANTONIO TX 78205 | Providing independent review of clinical trials for business purposes; Business consulting and management in the field of clinical trials, namely, providing information management services; Business consulting and management in the field of clinical trials, namely, management and compilation of computerized databases in the field of clinical trials for business purposes; Business consulting and management in the field of clinical trials, namely, clinical data and regulatory submission management on behalf of medical, biopharmaceutical and biotechnology companies to assist them with clinical research, clinical trials and applications for drug approval; Providing consulting services in the field of regulatory submission management to medical companies to assist them with applications for medical device approval; Regulatory submission management, namely, assisting others in preparing and filing applications for new drugs with governmental regulatory bodies; Providing business intelligence services in the fields of medical devices and pharmaceuticals;Regulatory compliance consulting in the field of medical products; Regulatory compliance consulting in the field of prescription drug sampling;Medical and scientific research, namely, conducting clinical trials for others; Providing medical and scientific research information in the field of clinical trials; Providing medical and scientific research information in the field of pharmaceuticals and clinical trials; Conducting research and clinical trials for others relating to medical devices and pharmaceuticals in the fields of oncology, immunology, military medicine, emergency medicine, critical care, regenerative medicine, infectious disease; Consulting services for others in the field of design, planning, and implementation project management of scientific research and clinical trials; Medical research; Scientific research and development; Biomedical research services; Providing information about medical and scientific research; Research and development of vaccines and medicines; Consulting services in the fields of biotechnology and pharmaceutical research and development; Pharmaceutical research and development; Pharmaceutical drug development services; Technical research in the field of pharmaceutical studies; Conducting early evaluations in the field of new pharmaceuticals; Development of pharmaceutical preparations and medicines; |
| MAGIC TRIAL | Kiromic, Inc. | Trish Faulkner 7707 Fannin Street, Suite 140 Houston TX 78257 | Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research; |
| MARK-T TRIAL | Kiromic, Inc. | Trish Faulkner 7707 Fannin Street, Suite 140 Houston TX 78257 | Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research; |
| NEW ENGLAND INDEPENDENT REVIEW BOARD | WESTERN INSTITUTIONAL REVIEW BOARD, INC. | 1019 39TH AVENUE SE SUITE 120 PUYALLUP WA 98374 | Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research;INDEPENDENT REVIEW BOARD; |
| NEW ENGLAND INSTITUTIONAL REVIEW BOARD | NEW ENGLAND INDEPENDENT REVIEW BOARD | 202 CARNEGIE CENTER SUITE 107 PRINCETON NJ 08540 | Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research;INSTITUTIONAL REVIEW BOARD; |
| PRIME REVIEW BOARD SERVICES | THE EMMES COMPANY | 401 North Washington Street, Suite 700 Rockville MD 20850 | Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research;REVIEW BOARD SERVICES; |
| TOUR | CUMBERLAND PHARMACEUTICALS INC. | Suite 1300 1600 West End Avenue Nashville TN 37203 | Providing independent review of clinical trials for business purposes; business consulting and management in the field of clinical trials, namely, providing information management services; promoting exchange of information and resources within the scientific research and medical communities to achieve advances in the field of healthcare;Providing an on-line searchable database featuring health-related information relating to use of antibiotics; providing medical profiles and medical record analysis and assessments via a website that are designed to provide custom tailored outputs about recommended resources and treatments associated with a defined set of symptoms and concerns; providing an online, patient-initiated, patient-authorized, medical profile and medical record analysis service designed to provide patients with custom tailored information about the range of possible diagnoses and therapies associated with a defined set of symptoms; providing an online, healthcare practitioner-initiated, medical profile and record analysis service designed to monitor antibiotic treatment patterns, clinical effectiveness and safety outcomes;Providing an on-line searchable database in the field of clinical trials for scientific research purposes; providing medical and scientific research information in the field of pharmaceuticals and clinical trials; |
| TRAUMA INSIGHT | Trauma Insight | 1305 East Houston Street San Antonio TX 78205 | Providing independent review of clinical trials for business purposes; Business consulting and management in the field of clinical trials, namely, providing information management services; Business consulting and management in the field of clinical trials, namely, management and compilation of computerized databases in the field of clinical trials for business purposes; Business consulting and management in the field of clinical trials, namely, clinical data and regulatory submission management on behalf of medical, biopharmaceutical and biotechnology companies to assist them with clinical research, clinical trials and applications for drug approval; Providing consulting services in the field of regulatory submission management to medical companies to assist them with applications for medical device approval; Regulatory submission management, namely, assisting others in preparing and filing applications for new drugs with governmental regulatory bodies; Providing business intelligence services in the fields of medical devices and pharmaceuticals;Regulatory compliance consulting in the field of medical products; Regulatory compliance consulting in the field of prescription drug sampling;Medical and scientific research, namely, conducting clinical trials for others; Conducting clinical trials for others; Providing medical and scientific research information in the field of clinical trials; Providing medical and scientific research information in the field of pharmaceuticals and clinical trials; Conducting research and clinical trials for others relating to medical devices and pharmaceuticals; Consulting services for others in the field of design, planning, and implementation project management of scientific research and clinical trials; Medical research; Scientific research and development; Biomedical research services; Providing information about medical and scientific research; Research and development of vaccines and medicines; Consulting services in the fields of biotechnology and pharmaceutical research and development; Pharmaceutical research and development; Pharmaceutical drug development services; Technical research in the field of pharmaceutical studies; Conducting early evaluations in the field of new pharmaceuticals; Development of pharmaceutical preparations and medicines; |
| WCG IRB | WIRB-Copernicus Group, Inc. | 212 Carnegie Center, Suite 301 Princeton NJ 08540 | Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research; reviewing the safety and ethics of research protocols for bio-pharmaceutical and medical device testing on humans, namely, investigating testing procedures, staff qualifications and consent forms; reviewing standards and practices to assure regulatory compliance with international and federal regulations relating to clinical studies involving humans and informed consent;Providing an on-line database featuring healthcare research information;IRB;Providing a web site featuring technology for use by others to manage and exchange healthcare research information; providing use of non-downloadable computer software via the internet for managing healthcare research and support information; services in the field of compliance with international and federal regulations and guidelines in the nature of development of quality control standards relating to clinical studies involving humans and informed consent; Providing an on-line database featuring healthcare in the nature of medical research information; |
Where the owner name is not linked, that owner no longer owns the brand |
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