SOCRA CCRP Practice Exam

ICH GCP (International Conference on Harmonization Good Clinical Practice) provides guidelines for clinical trials. One of the key requirements for sponsors is to ensure proper accountability for investigational product (IP) throughout the trial. This includes ensuring timely delivery of IP to investigators, maintaining records of shipment, receipt, disposition, return and destruction, maintaining systems for retrieving and disposition of unused IP, ensuring IP stability, and maintaining sufficient quantities of IP. Options A, C, and D are incorrect as they are not relevant to the requirements for sponsors regarding IP accountability.