Good Clinical Practice

The In drug development and production, good clinical practice (GCP) is an international quality standard which governments can then transpose into regulations for clinical trials involving human subjects.

It is designed to protect patients and ensure the integrity of clinical trials. GCP applies to all stages of research, including design, conduct, performance, monitoring, auditing, recording, analyses, and reporting of research involving people. It provides a structured system that helps researchers conduct studies with accuracy and transparency, ensuring ethical rules are followed while maintaining the quality of collected data.