A pharmaceutical company begins a clinical trial to test a n…
A pharmaceutical company begins a clinical trial to test a new cancer medicine in South Africa. During the study, investigators ensure that all participants provide informed consent, patient information is accurately recorded, adverse events are monitored, and the trial follows approved scientific and ethical procedures. Regulatory inspectors later review the study to confirm that participant rights were protected and that the trial results are reliable. Why is it important to comply with Good Clinical Practice (GCP) when conducting clinical trials?