North Carolina Statutes
§ 90-325.31 — Authorized access to and use of individualized investigational drugs, biological products, or devices
North Carolina § 90-325.31
This text of North Carolina § 90-325.31 (Authorized access to and use of individualized investigational drugs, biological products, or devices) is published on Counsel Stack Legal Research, covering North Carolina primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.
Bluebook
N.C. Gen. Stat. § 90-325.31 (2026).
Text
(a)A manufacturer operating within an eligible facility and in accordance with all applicable federal law may make available to an eligible patient, and an eligible patient may request, the manufacturer's individualized investigational drug, biological product, or device from an eligible facility or manufacturer operating within an eligible facility. However, nothing in this Part shall be construed to require a manufacturer of an individualized investigational drug, biological product, or device to make such individualized investigational drug, biological product, or device available to an eligible patient.
(b)A manufacturer of an individualized investigational drug, biological product, or device may provide the individualized investigational drug, biological product, or device to an eli
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Nearby Sections
15
§ 90-1.1
Definitions§ 90-10.1
Examinations accepted by the Board§ 90-100
Rules§ 90-105
Order forms§ 90-106
Prescriptions and labelingCite This Page — Counsel Stack
Bluebook (online)
North Carolina § 90-325.31, Counsel Stack Legal Research, https://law.counselstack.com/statute/nc/90/90-325.31.