question archive Read the ICH GCP guidance: ICH E6 R2: https://www
Read the ICH GCP guidance: ICH E6 R2: https://www
Subject:BiologyPrice: Bought3
Read the ICH GCP guidance: ICH E6 R2: https://www.fda.gov/files/drugs/published/E6%28R2%29-Good-Clinical-Practice--Integrated-Addendum-to-ICH-E6%28R1%29.pdfLinks to an external site. You work at a small organization and are the sponsor of a phase 3 study for which have hired a CRO to help run the clinical trial. Discuss the compliance-related activities related to delegation of duties to the CRO that you would need to undertake in order to conduct the study in accordance with the GCP guidance.
