How should clinical trial data be recorded according to GCP?

Recording clinical trial data accurately and promptly is essential for ensuring the integrity and reliability of the research findings. According to Good Clinical Practice (GCP) guidelines, the accuracy of data reflects the credibility of the trial results, as any errors or delays can significantly impact the interpretation of the study and potential patient safety.

Prompt recording of data helps in maintaining the continuity and consistency of the trial, allowing for timely analysis and decision-making. In a clinical trial, it's crucial to capture participant responses, adverse events, and other pertinent information as soon as possible after they occur, thus minimizing the risk of memory bias or data degradation.

Adhering to this principle not only complies with regulatory expectations but also fosters transparency in clinical research, which is fundamental for regulatory submissions and for building trust with stakeholders, including participants and regulatory bodies.