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.
S.C. Code Ann. § 44-33-340
Prohibited use of registry information
2022 Act No. 206 (H.3166), SECTION 2, eff May 23, 2022.
Official source: South Carolina Legislature. Reproduced from public-domain South Carolina statutes; confirm against the official source for the current text. Not legal advice.