Institutional Review Board Approval. Before any activities involving human subjects commence, the contractor will develop and submit protocols and materials for approval by the Public Health’s Institutional Review Board (IRB) and the Contractor’s IRB as applicable, to ensure that human subjects and their information are protected as required by law. Contractor must demonstrate that sufficient time is allotted for IRB review and approval.
Institutional Review Board Approval. Intracel shall cooperate with Medical Director in preparing and filing research protocols, informed consent form, and other information with Hospital's Institutional Review Board ("IRB"). Medical Director shall apply for approval to conduct the research protocol with the IRB.
Institutional Review Board Approval. 9.1 Study Site shall ensure that the Investigator shall apply for approval to conduct the Study at the Study Site with Study Site’s designated Institutional Review Board (“IRB”) and shall not initiate the Study until such approval is obtained. Awardee shall cooperate with Investigator in preparing and filing the Protocol, informed consent form [***drafting note- can change to “waiver of informed consent form” if applicable to the Study***], and other required information with the IRB.
Institutional Review Board Approval. The Emory University Institutional Review Board deemed this study exempt from review due to its nature as a part of public health practice. Results Participants in this study (n=9) were state legislators representing areas in North, South, and Western Georgia, as well as parts of Metropolitan Atlanta. They had between 1 and 29 years of experience as legislators with a mean of 9 years. For three participants, the 2019 legislative session was their first. The sample included six females and three males, and participants identified as African-American or Black, and White. They were married, single, and divorced, and most reported having children. Based on party affiliation three participants were Republican and six were Democrat. All Republicans voted in favor of HB 481 and all Democrats voted against the bill. Four themes emerged inductively from the data. These included: factors influencing decision-making; existing beliefs about abortion influenced views of HB 481; communication about HB 481 was not effective in changing beliefs; and Democrats’ views on HB 481 were similar while Republicans’ views were varied. Figure 1. Association Between Factors that Influenced Decision-Making and Common Themes in the Research Factors that influenced legislators’ decision-making Four factors influenced legislators’ decision making when voting on HB 481: personal values including views on abortion, rights and the law, evidence, and their constituents. Personal values were the most commonly cited influences in how legislators voted. These included religious or faith beliefs about when life begins and the value of, “the life of the unborn.”
Institutional Review Board Approval. A. This Contract is authorized by, and in compliance with, the provisions of Texas Government Code Section 531.039. The project falls within the purview of the program, as the public health purpose of the project is to provide a research study of assessing medication needs and the potential barriers to accessing medications within a population of uninsured and underinsured patients in Texas.
Institutional Review Board Approval. Institutional Review Board (IRB) review for all research with human subjects is required. IRB approval may come from either university IRBs or independent IRBs.
Institutional Review Board Approval. Investigator shall apply for approval to conduct the Study with University’s Institutional Review Board ("IRB"). University shall not initiate the Study until such approval is obtained, and University is provided with a final copy of the IRB approval letter for the Study. University’s obligation to conduct the Study is expressly conditioned upon the approval of its IRB. University shall cooperate with Investigator in preparing and filing the Protocol, informed consent form, and other required information with the IRB.
Institutional Review Board Approval. Research may include designs for which informed consent must be obtained by participants. Any such proposal must be approved by the Commissioner of State, if applicable, by Contractor’s institutional review board, and, if applicable, by the Agency of Human Service’s institutional review board.
Institutional Review Board Approval. If necessary, Xxxxxx University will submit the Project for review and approval by its Institutional Review Board. In its discretion, Xxxxxx University may seek expedited approval.
Institutional Review Board Approval. When human subjects, tissues and/or materials are to be used in a research project, it is the responsibility of the MVP recipient to ensure that the company/institution has the following on file:
