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ICF tracking log setting

ICF tracking log is a functionality used to track the distribution, collection, and status of Informed Consent Forms (ICFs) from participants in the trial. It is a management tool that ensures proper documentation and completion of all steps related to informed consent throughout the trial process.

Using CTMS, you can create multiple tracking log templates and then associate a certain template with your study. This way, you can satisfy the evolving needs of your study and maintain ICF tracking log template versioning.

The specifics of the tracking log configurations you can learn in the following sections:

In this section:

A document that provides essential information about a clinical trial to potential participants to ensure their complete understanding of the research nature, the risks and potential benefits involved, and their rights as participants.

Before enrolling in a clinical trial, participants must read and understand the information in the ICF, and signing the ICF indicates their willingness to participate, understanding that they have been fully informed about the study.