S.C. Code Ann. § 44-33-340: Prohibited use of registry information.
Where this section sits in the code
- Title 44 - HEALTH
- CHAPTER 33 Sickle Cell Disease
- ARTICLE 3 Sickle Cell Disease Voluntary Patient Registry
The information maintained in the Sickle Cell Disease Voluntary Patient Registry may not be released to or used by an entity responsible for the licensure, regulation, or discipline of physicians or other health care practitioners for any purpose.
Collected 2026-09-02T07:32:19Z. Source file · JSON