Good Clinical Practices (GCP) refer to a set of ethical and scientific quality standards for designing, recording and reporting trials that involve the participation of human subjects. GCP guidelines define the responsibilities of sponsors, investigators, and ethics committees in conducting clinical research. These guidelines are essential to maintaining the rights, safety, and well -being of clinical trial participants and ensuring the validity and reliability of clinical trial data. Everyone involved in the conduct of clinical research must be competent to perform their tasks, qualified by education, training and experience. This training course will cover all aspects of GCP guidelines and ethical issues in conducting clinical research.

OBJECTIVE OF THE TRAINING COURSE:

An understanding of GCP is prerequisite for anyone carrying out, or involved in, clinical research and clinical trials.

Members of ethics committees, institutional review boards (IRBs), or research ethics boards (REBs) who review and approve clinical trial protocols should have a solid understanding of GCP principles. GCP training helps them evaluate the ethical aspects of proposed trials, ensuring participant rights, safety, and welfare.

WHY THIS TRAINING COURSE IS IMPORTANT FOR YOU?

GCP training course is now essential for all PG students and teaching faculties as per recent NMC Guidelines.

ICMR guideline also states that the members of IRB and Independent Ethics Committee (IEC) should have GCP training.

THE EXPECTED OUTCOME OF THE TRAINING COURSE:

Empower clinicians and researchers about basics of GCP and aware about current regulation and guidelines in India for Clinical Trials

Understand the key components of GCP including informed consent research protocol

Ensure  the  data  management  and  quality  assurance  policies  and practices involved in clinical research

One Week Date: 23 to 29  Oct, 2025.