An audit log is a chronological record of system activities that provides documentary evidence of the sequence of activities affecting an operation, procedure, or event. In clinical research, it serves as a critical tool for maintaining data integrity and regulatory compliance. The log captures details such as user actions, data modifications, and system events.
Audit logs are essential for tracking changes made to electronic records, identifying unauthorized access attempts, and reconstructing the sequence of events during a study. They play a crucial role in ensuring the traceability and accountability of clinical trial data, supporting Good Clinical Practice (GCP) guidelines and regulatory requirements for data management and security.
Audit logs are crucial in clinical research for ensuring data integrity and regulatory compliance. They provide a verifiable trail of all actions taken within a clinical trial management system, allowing investigators and auditors to detect and investigate any unauthorized changes or discrepancies in the data.
The importance of audit logs extends to facilitating regulatory inspections and supporting the overall quality and credibility of clinical trials. By maintaining a detailed record of user activities and system events, audit logs help demonstrate adherence to Good Clinical Practice (GCP) guidelines and enhance the transparency and reproducibility of research outcomes.
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