RAPS Regulatory Affairs Certification – Drugs (RAC‑Drugs) Practice Test 2026 - Free RAC-Drugs Practice Questions and Study Guide

The term "sponsor" in the context of clinical trials refers to the organization or individual that manages and finances the study. This entity is responsible for initiating, overseeing, and ensuring the compliance of the trial with regulatory standards. The sponsor often bears the costs associated with the trial, including funding for personnel, facilities, and other resources necessary for conducting the research.

This role is distinct from other participants in the trial, such as volunteers, who are individuals that consent to participate in the study, or regulatory agencies, which provide oversight to ensure the trial adheres to legal and ethical standards. The sponsor's responsibilities include study design, data management, and reporting results, making them a critical component in the functioning and success of clinical trials.