Good clinical practice (GCP) is an international quality standard, which governments can then transpose into regulations for clinical trials involving human subjects. GCP follows the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), and enforces ...
Before the GCP and similar regulations came into force, clinical trials were largely based on the needs of national governments rather than human rights. The GCP regulates human experimentation in the interest of advancing medical science. It acts as a quality benchmark as well as a moderator that keeps ...
Good Clinical Practice (GCP) is an internationally recognized quality standard. GCP standards include ethical, scientific and practical requirements in which all clinical research is conducted.
The primary principal of GCP is to ensure that the rights, safety and well-being of clinical trial subjects ...