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.
HISTORY: 2022 Act No. 206 (H.3166), Section 2, eff May 23, 2022.
Structure South Carolina Code of Laws
Chapter 33 - Sickle Cell Anemia
Section 44-33-10. Sickle cell education and prevention program.
Section 44-33-310. Development and maintenance of Sickle Cell Disease Voluntary Patient Registry.
Section 44-33-330. Confidentiality of information submitted to registry; permitted disclosures.
Section 44-33-340. Prohibited use of registry information.
Section 44-33-350. Revocation of registration.
Section 44-33-360. Physicians prohibited from accessing registry without patients' request.
Section 44-33-370. Obligation to update contact information.