Investigational product dispensing or administration information for the sponsor is recorded on which document?

The case report form is the correct document for recording investigational product dispensing or administration information for the sponsor. This document plays a crucial role in clinical trials, as it collects data on the administration of the investigational product, including details such as dosage, timing, and any adverse reactions observed in participants.

The case report form serves as a primary data collection tool in clinical trials, ensuring that all pertinent information related to the investigational product's usage is systematically documented. This thorough documentation is essential for the analysis of the investigational product's safety and efficacy, which is ultimately used in decision-making regarding the product's approval.

In contrast, other documents such as form FDA 1572, while important for ensuring compliance with regulatory requirements and providing investigational site information, do not specifically focus on the detailed tracking of product dispensing or administration. The informed consent form is designed to ensure that participants understand the study and agree to partake in it, while the insurance claim form pertains to reimbursement for medical services rather than investigational product administration. Thus, the case report form remains the appropriate choice for this specific purpose in clinical research.