Mastering ICH Good Clinical Practice E6 (R2)

The following Mastering ICH Good Clinical Practice E6 (R2) is designed to educate healthcare providers (HCP) on the ICH guidelines for good clinical practice (GCP).What you will learn: Ethical principles underpinning the ICH GCP guidelines Responsibilities and expectations for all parties involved in clinical trials Critical aspects of clinical trial design The process of obtaining informed consent from trial participants Best practices for conducting clinical trials in accordance with the ICH GCP guidelines The importance of accurate data collection Processes for ongoing trial monitoring