Abstract
One area of deliberation undertaken by the International Conference on Harmonization (ICH) Member States is the formulation of international and scientific quality standards for designing, conducting, recording, and reporting trials that involve the participation of human subjects or the standards for good clinical practice (GCP). This paper presents an overview of the ICH GCP and a background summary of the ICH which is the matriarch of this GCP topic.
Get full access to this article
View all access options for this article.