A patient is obligated to update contact information that is maintained in the registry after initial registration by a physician in accordance with procedures established by the department.
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.