{"data":{"id":"us-tn/tenn.-code-ann.-63-6-309","jurisdiction":"us-tn","citation":"Tenn. Code Ann. § 63-6-309","heading":"Reporting of adverse events","body":"If a patient suffers an adverse event associated with the use of an investigational drug, biological product, or device, the patient's physician shall report the adverse event to the manufacturer of the investigational drug, biological product, or device.","path":["TN Code","Title 63","Chapter 6"],"source_url":"https://oss-data-us.vaquill.ai/v2026.08/us_tn_statutes.parquet","current_through":"2026-08-14","vintage":"open-us-law v2026.08, retrieved 2026-09-14","retrieved_at":"2026-09-14T18:32:26Z","sha256":"2eee7bdc999b421762af4dbe1be38f3821b6d94e54be0753b31ad983c9ecb146","source_id":"us-tn","stale":false,"prev":"us-tn/tenn.-code-ann.-63-6-308","next":"us-tn/tenn.-code-ann.-63-6-401"},"notice":"GroundRules: Original legal text. Not legal advice."}