Human Research Subject definition

Human Research Subject means a living person that an authorized user, conducting research, obtains data resulting from the intentional internal or external administration of radioactive material, or the radiation from radioactive material, to the individual. For the purpose of these rules, unless otherwise noted, the term patient applies to a human research subject.¶
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Human Research Subject means an individual who is or becomes a participant in research overseen by an IRB, either as a recipient of the test article or as a control. A subject may be either a healthy human, in research overseen by the RDRC, or a patient.
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Human Research Subject. An individual who has executed a written agreement to participate in an official University research program or project for compensation. Employees of the University who agree to be Human Research Subjects must be compensated thur Payroll.
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Examples of Human Research Subject in a sentence

  • We believe that the topics covered in the "Course in the Protection of Human Research Subject" are a beneficial adjunct to your current curriculum and will provide you with a strong research foundation.

  • Human Research Subject costs: indicate number of research subjects and incentive payment amount requested for each.

  • Data from the (1) Potential Total Value of Award and(2) Current Total Value of Award elements are extracted from FPDS-NG via the legacy USASpending.gov and provided to the Broker.1 Specifically, data for these elements are extracted from the following FPDS-NG fields, respectively: (1) base and exercised options value and (2) base and all options value.

  • To revise the questionnaire, the researcher used feedback received from her five dissertation committee members regarding the research instrument during the defense of her dissertation proposal and the preparation for her Human Research Subject proposal.

  • In addition, I understand that research at Louisiana State University, which involves human participation, is carried out under the oversight of the Institutional Review Board for Human Research Subject Protection.

  • NCBHR, “Protecting and Promoting the Human Research Subject: A Review of the Function of Research Ethics Boards in Canadian Faculties of Medicine” (1995) 6/1 NCBHR Communique 32.

  • Vasgird et al., Protecting the Uninsured Human Research Subject, 6(6) J.

  • Emmert, President, University of Washington, Re: Human Research Subject Protections Under Federalwide Assurance FWA-6878 (Apr.

  • President Level Administrative Regulations (AR):• AR 7:1 Research Misconduct• AR 7.2 Research Conflict of Interest and Financial Disclosure Policy• AR 7:4 Human Research Subject Protection and Institutional Review Boards• AR 7.9 Institutional Conflict of InterestB.

  • The documents required are as follow:• Letter from Purdue University Institutional Review Board• NASA/JSC Human Research Subject Informed Consent Forms for each subject• Anu Bhargava• Jonathan Andrew Wolter• Michael Lonnie Scott• Kimberly Louise Mrozek• Roy Byung-Kyu ChungThese documents are included in the Administrative Section IV part 5.0.


More Definitions of Human Research Subject

Human Research Subject means a human subject involved in research overseen by a RDRC, not including patients par- ticipating in a protocol involving an investigational new drug or device.
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Human Research Subject. An individual who has executed a written agreement to participant in anofficial University research program or project. Employees of the University who agree Human ResearchSubjects are not entitle to stipend payments if they are not receiving academic credit for their participationand must be compensated via approved documentation thru the University's' Human Resource Office.
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Related to Human Research Subject

  • scientific research means any activity in the field of natural or applied science for the extension of knowledge;

  • Development Team means the entities and professionals assembled to develop and manage the Project, typically including the Applicant, Owner, Developer(s), Co-Developer(s) and general partner or any other related entities in which the Developer or Co-Developer has an identity of interest or a Controlling Interest.

  • Joint Commercialization Committee or “JCC” has the meaning set forth in Section 2.1(a).

  • Research and development means (1) theoretical analysis, exploration, or experimentation; or (2) the extension of investigative findings and theories of a scientific or technical nature into practical application for experimental and demonstration purposes, including the experimental production and testing of models, devices, equipment, materials, and processes. Research and development does not include the internal or external administration of radiation or radioactive material to human beings.

  • Pivotal Clinical Trial means a pivotal human clinical trial of a Licensed Product with a defined dose or a set of defined doses of such Licensed Product designed to ascertain efficacy and safety of such Licensed Product for the purpose of enabling the preparation and submission of an MAA to the competent Regulatory Authorities in a country of the Territory, as further defined in 21 C.F.R. § 312.21(c) for the U.S., as amended from time to time, or the corresponding foreign regulations.

  • Research Program has the meaning set forth in Section 2.1.

  • Collaborative drug therapy management means participation by an authorized pharmacist and a physician in the management of drug therapy pursuant to a written community practice protocol or a written hospital practice protocol.

  • Medical Affairs Activities means, with respect to any country or other jurisdiction in the Territory, the coordination of medical information requests and field based medical scientific liaisons with respect to Licensed Compounds or Licensed Products, including activities of medical scientific liaisons and the provision of medical information services with respect to a Licensed Compound or Licensed Product.

  • Clinical Trials means a controlled study in humans of the safety or efficacy of a Product, and includes, without limitation, such clinical trials as are designed to support expanded labeling or to satisfy the requirements of an Agency in connection with any Product Approval and any other human study used in research and Development of a Product.

  • Collaboration Technology means all Collaboration Patents and Collaboration Know-How.

  • Commercialization or “Commercialize” means activities directed to marketing, promoting, research and development as required, manufacturing for sale, offering for sale, distributing, importing or selling a product, including sub-licensing or sub-contracting of these activities.

  • Clinical evaluation means a systematic and planned process to continuously generate, collect, analyse and assess the clinical data pertaining to a device in order to verify the safety and performance, including clinical benefits, of the device when used as intended by the manufacturer;

  • Economic development incentive means a financial incentive,

  • Collaboration has the meaning set forth in Section 2.1.

  • Clinical Trial means a Phase I Clinical Trial, Phase II Clinical Trial or Phase III Clinical Trial, or any post-approval human clinical trial, as applicable.

  • Public research university means Rutgers, The State University

  • Joint Research Committee or “JRC” has the meaning set forth in Section 3.1.1.

  • Development Program means the implementation of the development plan.

  • Development Activity means any activity defined as Development which will necessitate a Floodplain Development Permit. This includes buildings, structures, and non-structural items, including (but not limited to) fill, bulkheads, piers, pools, docks, landings, ramps, and erosion control/stabilization measures.

  • Mobile crisis outreach team means a crisis intervention service for minors or families of minors experiencing behavioral health or psychiatric emergencies.

  • Global Development Plan has the meaning set forth in Section 3.1.

  • Clinical means having a significant relationship, whether real or potential, direct or indirect, to the actual rendering or outcome of dental care, the practice of dentistry, or the quality of dental care being rendered to a patient;

  • Phase III Clinical Trials means a Clinical Trial for the Product on sufficient numbers of patients to generate safety and efficacy data to support Regulatory Approval in the proposed therapeutic indication, conducted in accordance with current good clinical practices and in accordance with a protocol that has been reviewed by the FDA and reflects any comments or concerns raised by the same.

  • Phase 4 Clinical Trial means a Clinical Study in any country which is conducted after Regulatory Approval of a product has been obtained from an appropriate Regulatory Authority, consisting of trials conducted voluntarily for enhancing marketing or scientific knowledge of an approved indication and trials conducted due to request or requirement of a Regulatory Authority.

  • Medical evaluation means the process of assessing an individual's health status that includes a medical history and a physical examination of an individual conducted by a licensed medical practitioner operating within the scope of his license.

  • Research and development facility means an establishment engaged in laboratory, scientific, or experimental testing and development related to new products, new uses for existing products, or improving existing products. The term does not include an establishment engaged in efficiency surveys, management studies, consumer surveys, economic surveys, advertising, promotion, banking, or research in connection with literary, historical, or similar projects.