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 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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Examples of Human Research Subject in a sentence

  • The researcher used the feedback they gave her during the defense of her proposal and the preparation for her Human Research Subject proposal to determine how well the items represented the intended content areas.

  • 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.

  • An investigator with a formal appointment at UPHDM, or any of its components, wishing to conduct research at another institution, must follow the Policies and Procedures for Protection of Human Research Subject at both institutions.

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

  • Human Research Subject Participation Certification Certificate of ConfidentialitySubject Screening Log Monitor LogMajor Correspondence (SAE Reports, DSMB Reports, Protocol Amendments) Monitor Name: Monitor Signature: Date: Additional Comments:Laboratory Normals for the A2ALL Cohort Protocol Please supply the DCC and maintain a copy in your regulatory binder a list of the following laboratory normals.

  • Approval to conduct the study was granted by Ethic Review Board Committee for Research Involving Human Research Subject, Boromarajonani College of Nursing Nopparat Vajira.

  • The clinical collection site maintains quality control via standard operating procedures as defined by the protocols found in this document, protocols in the Manual of Procedures and in Institutional Human Research Subject SOPs. Each institution will establish internal quality control systems to ensure that from the start of screening, subject enrollment and specimen collection, the protocols are implemented consistently and with a high degree of accuracy.

  • After approval and permission letter were granted by Ethics Review Board Committee for Research Involving Human Research Subject, Boromarajonani College of Nursing Nopparat Vajira, the activity of public nursing home was followed to meet the respondents.

  • All research protocols involving investigational drugs or devices, or Investigator-designed projects (e.g., case reviews whether or not intended for publication, chart reviews that are preparatory to research) that may possibly qualify as “research” and involve “human subjects” as defined by the Health and Human Services’ (HHS’) Office of Human Research Subject Protection (OHRP).

  • In accordance with the Human Research Subject Protection Act of 1997, it is not possible to find out the exact ethnic background of the individual donors from whom the public and Celera genome sequences were derived.


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 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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Related to Human Research Subject

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

  • Clinical Development means the conduct of clinical trials in humans to assess the dosing, safety and/or efficacy of the Product, including but not limited to Phase I Clinical Trials, Phase II Clinical Trials, Phase Ill Clinical Trials and Phase IV Clinical Trials.

  • 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 3.4 (Joint Commercialization Committee).

  • 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 human clinical trial in any country that is prospectively designed to generate data intended to satisfy the requirements of 21 C.F.R. § 312.21(c) (as amended) in the U.S. or a similar clinical study prescribed by a Regulatory Authority from another country, from time to time, pursuant to Applicable Law.

  • Research Program has the meaning set forth in Section 3.1.

  • 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;

  • Collaboration has the meaning set forth in Section 2.1.

  • Licensed assistant behavior analyst means a person who holds current certification or meets the standards to be certified as a board certified Assistant Behavior Analyst issued by the Behavior Analyst Certification Board, Inc., or any successor in interest to that organization, who is licensed as an Assistant Behavior Analyst by the Board of Psychological Examiners and who provides Behavioral Therapy under the supervision of a Licensed Behavior Analyst or psychologist.

  • Clinical Trial means any human clinical trial of a Product.

  • 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.

  • 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 Trial of a Product conducted after Regulatory Approval of such Product has been obtained from an appropriate Regulatory Authority, which trial is (a) conducted voluntarily by a Party to enhance marketing or scientific knowledge of the Product, or (b) conducted due to a request or requirement of a Regulatory Authority.

  • 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.

  • Phase I Clinical Trial means a human clinical trial that is intended to initially evaluate the safety and/or pharmacological effect of a Product in subjects or that would otherwise satisfy requirements of 21 C.F.R. 312.21(a), or its foreign equivalent.