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This article walks through the setup and implementation of Consent. 

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The eConsent function will only work if the study is an ePRO study where the subject email is getting registered on the registration form. Read more about configuring ePRO here.

Like most functions, the first step is to ensure your role has the appropriate role permissions to configure the consent rules. This is done in role security under the Informed Consent application.

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The mobile app subject manager will indicate which subjects are consented, not consented, or using paper consent.

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Further reading

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As patients Participants become registered in the study and consented, it will be tracked in the consent report

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