Clinical trials are a crucial aspect of the FDA's regulatory process for approving new drugs and medical devices. Topics in this area may include informed consent, Institutional Review Boards (IRBs), and Good Clinical Practice (GCP) guidelines.
Clinical trials are a crucial aspect of the FDA's regulatory process for approving new drugs and medical devices. Topics in this area may include informed consent, Institutional Review Boards (IRBs), and Good Clinical Practice (GCP) guidelines.