Good clinical practice

From WikiMD's medical encyclopedia

Good Clinical Practice (GCP) is an international ethical and scientific quality standard for designing, conducting, recording, and reporting trials that involve the participation of human subjects. Compliance with this standard provides public assurance that the rights, safety, and well-being of trial subjects are protected, consistent with the principles that have their origin in the Declaration of Helsinki, and that the clinical trial data are credible.

Overview

The principles of Good Clinical Practice (GCP) help to ensure the safety, integrity, and quality of clinical trials by addressing elements related to the design, conduct, and reporting of clinical trials. GCP guidelines are not laws, but rather, standards that are recognized and accepted worldwide by regulatory authorities, researchers, and the pharmaceutical industry.

Principles of Good Clinical Practice

The principles of Good Clinical Practice (GCP) include:

  • Respect for the dignity, rights, safety, and well-being of research participants
  • Scientifically sound and clearly described trial design
  • Careful assessment of the balance of risks and benefits
  • Independent review of proposed research
  • Conduct of the trial in compliance with the approved protocol
  • Use of data that are accurate, complete, and verifiable
  • Confidentiality of participant information
  • Access to emergency care for participants, if necessary
  • Compliance with all regulatory requirements
  • Quality assurance and quality control systems
  • Adequate record keeping
  • Adherence to the ethical principles outlined in the Declaration of Helsinki

Importance of Good Clinical Practice

Good Clinical Practice (GCP) is important because it establishes standards for clinical trials that protect the rights, safety, and welfare of study participants. It also ensures the integrity and credibility of the data collected in the trial. Compliance with GCP provides public assurance that the rights, safety, and well-being of trial subjects are protected.

See Also

References


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Contributors: Prab R. Tumpati, MD