What does GCP stand for in clinical trials?

Good Clinical Practice (GCP) is a set of international ethical and scientific quality standards that govern the design, conduct, recording, and reporting of clinical trials involving human subjects. It ensures that the rights, safety, and well-being of trial participants are protected and that the data generated from trials is credible and reliable.

GCP encompasses a variety of requirements, including the proper informed consent processes, adherence to legal and regulatory obligations, and the necessity of maintaining integrity in clinical trial data. It is essential for ensuring that trials are conducted consistently in accordance with the established protocols and regulatory requirements, thus promoting the integrity of the research.

In contrast, other terms like General Clinical Procedures or Guidelines for Clinical Production do not refer to a recognized regulatory framework and lack established definitions or guidelines in the context of clinical trials. The term Good Compliance Protocol does not accurately reflect the comprehensive standards encapsulated in GCP. Thus, the identification of GCP as Good Clinical Practice is crucial for professionals involved in clinical research.