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Protocol 20210057 November 30, 2022 Page 1 of 17Informed ConsentINFORMED CONSENT/AUTHORIZATION FOR PARTICIPATION IN RESEARCH WITH OPTIONAL PROCEDURES Phase II trial of sitravatinib plus nivolumab
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The consent form typically contains information regarding the permissions granted by the signer, including the purpose of the consent, the parties involved, and any potential risks or consequences.
Individuals or entities that are involved in activities requiring consent, such as medical treatments, research participation, or data sharing, are required to file this consent form.
To fill out the consent form, follow these steps: read the instructions carefully, provide necessary personal information, sign and date the form, and ensure any required witnesses sign as well.
The purpose of the consent form is to obtain the explicit permission of the signer for a specific action or process, ensuring that they are informed of their rights and any associated risks.
The information that must be reported on this consent form typically includes the signer’s identity, details of the consented activity, any potential risks, and the rights of the signer.
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