The Office of Clinical Research has recently introduced updated clinical research policies and standard operating procedures for the Midwest and Southeast regions. These comprehensive policies cover essential areas such as subject screening and enrollment, adverse event reporting, record management, informed consent, IRB submissions, honest broker certification, and regulatory audit procedures.
The unified approach ensures consistency and compliance across our enterprise, strengthening our commitment to high-quality research and patient safety. Please review the new policies to stay informed and ensure alignment with the latest standards in clinical research.
For more information or questions, please reach out to Amy Hughes at Amy.Hughes@AdvocateHealth.com.