Newborn Screening Saves Lives Reauthorization Act of 2013
AN ACT
To amend the Public Health Service Act to reauthorize programs under part A of title XI of such Act.
2. Improved newborn and child screening and follow-up for heritable disorders
“(5) to improve the timely collection, delivery, receipt, and screening of specimens, and the timely diagnosis of heritable disorders in newborns.”
3. Evaluating the effectiveness of newborn and child screening and follow-up programs
“(4) methods that may be identified to improve quality in the diagnosis, treatment, and disease management of heritable disorders based on gaps in services or care; or
“(5) methods or best practices by which the eligible entities described in section 1109 can achieve the timely collection, delivery, receipt, and screening of newborn screening specimens, and the timely diagnosis of heritable disorders in newborns.”
4. Advisory committee on heritable disorders in newborns and children
“(4) provide technical assistance, as appropriate, to individuals and organizations regarding the submission of nominations to the uniform screening panel, including prior to the submission of such nominations;”
“(L) the timely collection, delivery, receipt, and screening of specimens to be tested for heritable disorders in newborns in order to ensure rapid diagnosis and follow-up.”
“(3) Deadline for review—For each nomination to the recommended uniform screening panel, the Advisory Committee on Heritable Disorders in Newborns and Children shall review and vote on the nominated condition within 9 months of the date on which the Advisory Committee referred the nomination to the condition review workgroup.”
“(f) Meetings—The Advisory Committee shall meet at least 4 times each calendar year, or as subject to the discretion of the Designated Federal Officer in consultation with the Chair.”
5. Clearinghouse of Newborn Screening Information
“(4) maintain current information on the number of conditions for which screening is conducted in each State; and
“(5) disseminate available evidence-based guidelines related to diagnosis, counseling, and treatment with respect to conditions detected by newborn screening.”
6. Laboratory quality and surveillance
“(b) Surveillance activities—The Secretary, acting through the Director of the Centers for Disease Control and Prevention, and taking into consideration the expertise of the Advisory Committee on Heritable Disorders in Newborns and Children established under section 1111, may provide, as appropriate, for the coordination of surveillance activities, including—
“(1) through standardized data collection and reporting, as well as the use of electronic health records; and
“(2) by promoting data sharing regarding newborn screening with State-based birth defects and developmental disabilities monitoring programs.”
7. Interagency Coordinating Committee on Newborn and Child Screening
8. National contingency plan for newborn screening
9. Hunter Kelly Research Program
“(C) by providing research findings and data for newborn conditions under review by the Advisory Committee on Heritable Disorders in Newborns and Children to be added to the recommended uniform screening panel;
“(D) conducting pilot studies on conditions recommended by the Advisory Committee on Heritable Disorders in Newborns and Children to ensure that screenings are ready for nationwide implementation; and”
10. Authorization of appropriations
“1117. Authorization of appropriations for newborn screening programs and activities
“There are authorized to be appropriated—
“(1) to carry out sections 1109, 1110, 1111, and 1112, $18,334,000 for each of fiscal years 2014 through 2018; and
“(2) to carry out section 1113, $7,500,000 for each of fiscal years 2014 through 2018.”