{"data":{"id":"us-in/ic-16-38-2-6","jurisdiction":"us-in","citation":"IC 16-38-2-6","heading":"Additional information requests; individual patients; consent","body":"Sec. 6. Researchers may, with the approval of the state department, use the names of individual cancer patients when requesting additional information for research purposes or soliciting an individual patient's participation in a research project. However, if a researcher requests additional information for an individual cancer patient's participation in a research project, the researcher must first obtain the oral or written consent of the patient's attending physician. If the consent of the patient's attending physician is obtained, the researcher must then obtain the individual cancer patient's written consent by having the patient complete a release of confidential medical information form.","path":["TITLE 16. HEALTH","ARTICLE 38. HEALTH REGISTRIES","Chapter 2. Cancer Registry"],"source_url":"https://iga.in.gov/ic/2026/Title_16.html#16-38-2-6","current_through":"2026","vintage":"2026","retrieved_at":"2026-09-11T20:02:18Z","sha256":"90d97b4f79775b8374a3383b0d69e1f725c82217832f0919fd0265d715ea22c7","source_id":"us-in","stale":false,"prev":"us-in/ic-16-38-2-5","next":"us-in/ic-16-38-2-7"},"notice":"GroundRules: Original legal text. Not legal advice."}