The principles of GCP are designed to be flexible and applicable to a
broad range of clinical trials. The updated E6 guideline, along with
ICH E8, encourages thoughtful consideration and planning to address
specific and potentially unique aspects of an individual clinical trial. This
includes evaluation of trial characteristics, such as the design elements,
the investigational product being evaluated, the medical condition being
addressed, characteristics of the participants, the setting in which the
clinical trial is being conducted, and the type of data being collected.
Careful consideration of factors relevant to ensuring trial quality, including
critical-to-quality (CTQ) factors, are needed for each clinical trial. This
web seminar will provide a high-level overview of the drivers and changes
planned for implementation.