ICH-GCP for Clinical Research

Overview for ICH-GCP for Clinical Research

A brief description about this Activity.

Purpose: To equip researchers and clinical trial professionals with the knowledge of ethical and scientific standards crucial for conducting high-quality, ethical, and reliable clinical trials, ensuring the protection of human subjects' rights, safety, and well-being, and maintaining the integrity of clinical trial data. ICH GCP refers to the International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use's guideline for Good Clinical Practice (GCP), which establishes an international standard for designing, conducting, recording, and reporting clinical trials involving human participants. It aims to protect the rights, safety, and welfare of human subjects, minimize human exposure to investigational products, improve data quality, and expedite the marketing of new drugs. Compliance with ICH GCP provides public assurance that the rights, safety, and well-being of trial subjects are protected and that the clinical trial data is credible.

Website

Learn more about this Activity.

No Website has been provided for this Activity.

Provided By

The Provider for this Activity.