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ICF tracking log template

ICF tracking log is a document 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.

In CTMS, the process of ICF tracking and management is held individually for each study under the STUDY MANAGEMENT tab. However, from the library, you can create sponsor-level templates for the ICF tracking log and reuse them per study as required.

In the library, you can perform different actions to the ICF tracking log as explained 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.