South Carolina General Assembly
117th Session, 2007-2008

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Bill 1108

Indicates Matter Stricken
Indicates New Matter

(Text matches printed bills. Document has been reformatted to meet World Wide Web specifications.)

INTRODUCED

February 14, 2008

S. 1108

Introduced by Medical Affairs Committee

S. Printed 2/14/08--S.

Read the first time February 14, 2008.

            

A JOINT RESOLUTION

TO APPROVE REGULATIONS OF THE DEPARTMENT OF HEALTH AND ENVIRONMENTAL CONTROL, RELATING TO SOUTH CAROLINA BIRTH DEFECTS PROGRAM, DESIGNATED AS REGULATION DOCUMENT NUMBER 3151, PURSUANT TO THE PROVISIONS OF ARTICLE 1, CHAPTER 23, TITLE 1 OF THE 1976 CODE.

Be it enacted by the General Assembly of the State of South Carolina:

SECTION    1.    The regulations of the Department of Health and Environmental Control, relating to South Carolina Birth Defects Program, designated as Regulation Document Number 3151, and submitted to the General Assembly pursuant to the provisions of Article 1, Chapter 23, Title 1 of the 1976 Code, are approved.

SECTION    2.    This joint resolution takes effect upon approval by the Governor.

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SUMMARY AS SUBMITTED

BY PROMULGATING AGENCY.

New Regulation 61-114 was promulgated to implement provisions of the South Carolina Birth Defects Act (2004 S.C. Act No. 281) codified at S.C. Code Ann. Sections 44-44-10 through -160, regarding the public health surveillance of birth defects identified in children up to two years of age in South Carolina. This legislative mandate authorizes the Department to promulgate regulations for public health surveillance of birth defects and to ensure compliance with the public health monitoring of every child born in South Carolina. Specific areas which the Department seeks to address in the regulations include: Definitions of key terms; establishment of the South Carolina Birth Defects Program; purpose of the program and type of case ascertainment utilized; utilization of data; methods of referral and intervention; establishment and composition of the South Carolina Birth Defects Advisory Council; maintenance of central database; access to health and medical records; confidentiality; public reports of de-identified, aggregate data; use and disclosure of birth defects data; and agreements with other agencies.

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