What does "Good Clinical Practice" (GCP) ensure in clinical trials?

"Good Clinical Practice" (GCP) ensures credible and accurate data reporting in clinical trials, which is essential for maintaining the integrity and reliability of research findings. GCP is an international quality standard that encompasses various aspects of clinical trials, including the ethical and scientific quality of the studies being conducted. By adhering to GCP guidelines, researchers ensure that the data collected is accurate, verifiable, and can be used to make informed decisions about the safety and efficacy of the intervention being studied. This compliance fosters confidence in the results among stakeholders, including regulatory authorities, sponsors, and the public, while also ensuring the protection of trial participants.

Other options focus on different aspects that, while important, do not align directly with the core principles of GCP. High enrollments, speedy completion, and profit maximization are secondary outcomes that may be desirable, but they are not the primary objectives of GCP itself. The primary emphasis of GCP is on the integrity of the research process and the reliability of data collected within that framework.