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Clinical trials are essential for developing new treatments and improving health outcomes for patients. However, conducting a clinical trial is not a simple task. It requires careful planning, execution, and reporting to ensure the quality and validity of the data and the safety and well-being of the participants. This is where Good Clinical Practice (GCP) comes in. GCP is an international ethical and scientific quality standard for designing, conducting, recording and reporting trials that involve the participation of human subjects 1 . GCP aims to provide a unified standard for the ICH regions (the European Union, Japan, the United States, Canada, Switzerland, Brazil, Australia and South Korea) to facilitate the mutual acceptance of clinical data by the regulatory authorities in these jurisdictions 2 . GCP is based on the principles of respect for human dignity, protection of human rights, and assurance of the welfare of the participants 2 . GCP also ensures that the data generated f...
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