Common use of USE OF HUMAN SUBJECTS (if applicable Clause in Contracts

USE OF HUMAN SUBJECTS (if applicable. 12.1 University will conduct all research in accordance with Federal Wide Assurance #2030, written protocol, applicable law, and University’s ethical standards. In the event a research participant has a research related injury neither University nor the Sponsor are responsible for any resulting medical care. 12.2 During and for a period of at least two years after completion of the study, the Sponsor must promptly report to the Principal Investigator any information that could: Affect the safety of the participants Affect the willingness of research participants to continue participation Influence the conduct of the study Alter the IRB’s approval for the study 12.3 In the event research findings indicate that current and past participants are at increased risk that was not anticipated at the time of the study design, the Principal Investigator, in accordance with both University IRB Policy and Procedures and the informed consent agreement, will immediately inform research participants of risk alteration.

USE OF HUMAN SUBJECTS (if applicable. 12.1 University will conduct all research in accordance with Federal Wide Assurance #2030, written protocol, applicable law, and University’s ethical standards. In the event a research participant has a research related injury neither University nor the Sponsor are responsible for any resulting medical care. 12.2 During and If the Sponsor is responsible for a period of at least two years after completion of the studymonitoring research, then the Sponsor must promptly report to the Principal Investigator any information that could: alert University’s Institutional Review Board (“IRB”) when research findings: (a) Affect the safety of the participants participants (b) Affect the willingness of research participants to continue participation participation (c) Influence the conduct of the study study (d) Alter the IRB’s approval for the study 12.3 In the event research findings indicate that current and past participants are at increased risk that was not anticipated at the time of the study design, the Principal Investigator, in accordance with both University IRB Policy and Procedures and the informed consent agreement, will immediately inform research participants of risk alteration.

USE OF HUMAN SUBJECTS (if applicable. 12.1 University will conduct all research in accordance with Federal Wide Assurance #2030, written protocol, applicable law, and University’s ethical standards. In the event a research participant has a research related injury neither University nor the Sponsor are responsible for any resulting medical care. 12.2 During and for a period of at least two years after completion of the study, the Sponsor must promptly report to the Principal Investigator any information that could: Affect the safety of the participants Affect the willingness of research participants to continue participation Influence the conduct of the study Alter the University Institutional Review Board’s (“IRB’s ”) approval for the study 12.3 In the event research findings indicate that current and past participants are at increased risk that was not anticipated at the time of the study design, the Principal Investigator, in accordance with both University IRB Policy and Procedures and the informed consent agreement, will immediately inform research participants of risk alteration.

USE OF HUMAN SUBJECTS (if applicable. 12.1 University will conduct all research in accordance with Federal Wide Assurance #2030, written protocol, applicable law, and University’s ethical standards. In the event a research participant has a research related injury neither University nor the Sponsor are responsible for any resulting medical care. 12.2 During and If the Sponsor is responsible for a period of at least two years after completion of the studymonitoring research, then the Sponsor must promptly report to the Principal Investigator any information that couldalert University’s Institutional Review Board (IRB) when research findings: Affect the safety of the participants Affect the willingness of research participants to continue participation Influence the conduct of the study Alter the IRB’s approval for the study 12.3 In the event research findings indicate that current and past participants are at increased risk that was not anticipated at the time of the study design, the Principal Investigator, in accordance with both University IRB Policy and Procedures and the informed consent agreement, will immediately inform research participants of risk alteration.

USE OF HUMAN SUBJECTS (if applicable. 12.1 University will conduct all research in accordance with Federal Wide Assurance #2030, written protocol, applicable law, and University’s ethical standards. In the event a research participant has a research related injury neither University nor the Sponsor are responsible for any resulting medical care. 12.2 During and If the Sponsor is responsible for a period of at least two years after completion of the studymonitoring research, then the Sponsor must promptly report to the Principal Investigator any information that couldalert University’s Institutional Review Board (“IRB”) when research findings: Affect the safety of the participants Affect the willingness of research participants to continue participation Influence the conduct of the study Alter the IRB’s approval for the study 12.3 In the event research findings indicate that current and past participants are at increased risk that was not anticipated at the time of the study design, the Principal Investigator, in accordance with both University IRB Policy and Procedures and the informed consent agreement, will immediately inform research participants of risk alteration.