Tennessee Statutes
§ 63-6-309 — Reporting of adverse events
Tennessee § 63-6-309
JurisdictionTennessee
Title63
This text of Tennessee § 63-6-309 (Reporting of adverse events) is published on Counsel Stack Legal Research, covering Tennessee primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.
Bluebook
Tenn. Code Ann. § 63-6-309 (2026).
Text
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.
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Legislative History
Added by 2015 Tenn. Acts, ch. 376, s 1, eff. 7/1/2015.
Nearby Sections
15
§ 63-1-101
Powers and duties§ 63-1-102
Chapter definitions§ 63-1-103
Application for licenses§ 63-1-104
Issuance of licenses§ 63-1-105
Signing of licenses§ 63-1-107
License renewals§ 63-1-109
Display of license or certificate of registration - Terminology used in signs and written material§ 63-1-111
Retirement§ 63-1-112
License and registration fees§ 63-1-114
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Bluebook (online)
Tennessee § 63-6-309, Counsel Stack Legal Research, https://law.counselstack.com/statute/tn/63-6-309.