South Carolina House Bill 3124 (Prior Session Legislation)

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Spectrum: Partisan Bill (Democrat 4-0)
Status: Introduced on January 10 2017 - 25% progression, died in committee
Action: 2017-01-10 - Referred to Committee on Medical, Military, Public and Municipal Affairs
Pending: House Medical, Military, Public and Municipal Affairs Committee
Text: Latest bill text (Introduced) [HTML]

Enact The "sickle Cell Disease Voluntary Patient Registry Act"; To Require The South Carolina Department Of Health And Environmental Control To Develop And Maintain A Sickle Cell Disease Voluntary Patient Registry In Which Patients Diagnosed With Sickle Cell Disease May Register; To Establish Requirements For A Physician To Submit The Name And Other Identifying Information Of A Patient Diagnosed With Sickle Cell Disease To The Registry; To Prohibit Release Of Information Contained In The Registry, With Exceptions; To Allow Access To Information In The Registry By, Among Others, Treating Physicians And Other Health Care Practitioners To Verify Patient Registration And Health Care Researchers; To Allow A Patient To Revoke A Registration; And For Other Purposes.

Sickle cell disease

Rep. John King [D]

Rep. William Clyburn [D]

Rep. Gilda Cobb-Hunter [D]

Rep. Robert Ridgeway [D]

Date	Chamber	Action
2017-01-10	House	Referred to Committee on Medical, Military, Public and Municipal Affairs
2017-01-10	House	Introduced and read first time
2016-12-15	House	Referred to Committee on Medical, Military, Public and Municipal Affairs
2016-12-15	House	Prefiled

Type	Source
Summary	https://www.scstatehouse.gov/billsearch.php?billnumbers=3124&session=122&summary=B
Text	https://www.scstatehouse.gov/sess122_2017-2018/prever/3124_20161215.htm