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2022 South Carolina Code of Laws
Title 44 - Health
Chapter 33 - Sickle Cell Anemia
Editor's Note
2022 Act No. 206, Section 1, provides as follows:
"SECTION 1. This act may be known and cited as the 'Rena Grant Sickle Cell Disease Voluntary Patient Registry Act'."
ARTICLE 1 General Provisions
Editor's Note
2022 Act No. 206, Section 1, provides as follows:
"SECTION 1. This act may be known and cited as the 'Rena Grant Sickle Cell Disease Voluntary Patient Registry Act'."
ARTICLE 3 Sickle Cell Disease Voluntary Patient RegistryEditor's Note
2022 Act No. 206, Section 1, provides as follows:
"SECTION 1. This act may be known and cited as the 'Rena Grant Sickle Cell Disease Voluntary Patient Registry Act'."
- Section 44-33-310. Development and maintenance of Sickle Cell Disease Voluntary Patient Registry.
- Section 44-33-320. Physicians shall notify patients of registry after diagnosis; registration requirements.
- 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.
- Section 44-33-380. Promulgation of regulations.
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