Location of Research Sample Clauses
The 'Location of Research' clause defines where research activities under an agreement are permitted to take place. Typically, it specifies the physical sites, such as particular laboratories, institutions, or geographic regions, where the research must be conducted, and may require prior approval for any changes to these locations. This clause ensures that all parties are aware of and agree to the research setting, which can be important for compliance with legal, ethical, or funding requirements, and helps manage oversight and accountability for the research activities.
Location of Research. Will the research project be undertaken in a Wellcome Trust Clinical Research Facility? If yes, please specify: YES o NO x
Location of Research. In conducting research under [Name of Faculty Research Mentor], the Postdoctoral Fellow shall operate in the [name of Department/Faculty].
Location of Research. CCIA hereby acknowledges that it has been informed by Panacela that the initial research to be conducted utilizing in connection with the projects listed on Exhibit B and utilizing the Technology and/or the Know-How will be conducted outside of Australia, in countries including, but not limited to, the United States and Russia. CCIA is not aware of any license that must be obtained prior to Panacela’s initiation of research activities.
Location of Research. Research to be conducted at locations other than approved performance sites may require a letter of support or another institution’s approval if personnel are engaged. See OHRP Engagement Guidance or contact ORRP at ▇▇▇▇▇▇▇▇▇▇▇▇▇@▇▇▇.▇▇▇ or ▇▇▇-▇▇▇-▇▇▇▇ for more information. Address ▇▇▇ ▇. ▇▇▇▇ ▇▇▇▇▇▇ Columbus, OH Address Research activities by Using OSU as IRB of record Letter of support / IRB approval Ohio State personnel only Uploaded Files Enter all Ohio State study team members below. External collaborators will be entered on a different page. Study team members should only be listed in one category (i.e., PI, co- investigator, or key personnel). Co-investigators and key personnel are defined as individuals who participate in the design, conduct, or reporting of human subjects research. At a minimum, include individuals who recruit participants, obtain consent, or who collect study data. Additional contacts can also serve in another role on the project. All individuals listed as Ohio State study team members will have access to all submitted information, including completion status of team members’ administrative and training requirements (CITI, RCR, COI disclosure), and may edit submissions on behalf of the principal investigator. Electronic signatures are required of all Ohio State investigators named on the submission. Contact Information Email: ▇▇▇▇▇▇.▇@▇▇▇.▇▇▇ Phone: Academic Information Graduate Fellow (4875) Graduate School | Administration (cc10511) Conflict of Interest (COI) ✓ Completed (Expires: 06/30/2023) Activities Performed Academic Affairs (Academic_Affairs_CCH6) 0% FTE Protocol development/study design; Recruitment; Assess participant eligibility; Obtain consent/parental permission/assent; Interview participants/administer surveys; Conduct follow-up visits; Data collection/entry/coding; Data analysis/interpretation; Reporting results; Manuscript preparation; Maintain regulatory documentation; Contact Information Email: ▇▇▇▇▇▇▇.▇@▇▇▇.▇▇▇ Phone: Conflict of Interest (COI) ✓ Completed (Expires: 06/30/2023) Pint House Activities Performed Academic Information Student 0% FTE Protocol development/study design; Recruitment; Assess participant eligibility; Obtain consent/parental permission/assent; Interview participants/administer surveys; Data collection/entry/coding; Data analysis/interpretation; Reporting results; Contact Information Email: ▇▇▇▇▇.▇▇▇@▇▇▇.▇▇▇ Phone: Conflict of Interest (COI) ✓ Completed (Expires: 06/30/2023) Activities Per...