To clarify the rules relating to newborn screening research and informed consent.
What it does: Adds SEC. __. INFORMED CONSENT FOR NEWBORN SCREENING RESEARCH at the end of the billWhat it changes
1 change to H.R. 1281 · shown in the bill's text
Adds SEC. __. INFORMED CONSENT FOR NEWBORN SCREENING RESEARCH at the end of the bill
Adds a sectionIn H.R. 1281 · Referred in Senate
Passed the House of Representatives June 24, 2014.
Inserted: SEC. __. INFORMED CONSENT FOR NEWBORN SCREENING RESEARCH.
Inserted: (a) In General.--Research on newborn dried blood spots shall be considered research carried out on human subjects meeting the definition of section 46.102(f)(2) of title 45, Code of Federal Regulations, for purposes of Federally funded research conducted pursuant to the Public Health Service Act until such time as updates to the Federal Policy for the Protection of Human Subjects (the Common Rule) are promulgated pursuant to subsection (c). For purposes of this subsection, sections 46.116(c) and 46.116(d) of title 45, Code of Federal Regulations, shall not apply.
Inserted: (b) Effective Date.--Subsection (a) shall apply only to newborn dried blood spots used for purposes of Federally funded research that were collected not earlier than 90 days after the date of enactment of this Act.
Inserted: (c) Regulations.--Not later than 6 months after the date of enactment of this Act, the Secretary of Health and Human Services shall promulgate proposed regulations related to the updating of the Federal Policy for the Protection of Human Subjects (the Common Rule), particularly with respect to informed consent. Not later than 2 years after such date of enactment, the Secretary shall promulgate final regulations based on such proposed regulations.
Original wording
At the end, add the following:
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As printed
SA 3976. Mr. REID (for Mr. Paul) proposed an amendment to the bill H.R. 1281, to amend the Public Health Service Act to reauthorize programs under part A of title XI of such Act; as follows:
At the end, add the following:
SEC. __. INFORMED CONSENT FOR NEWBORN SCREENING RESEARCH.
(a) In General.--Research on newborn dried blood spots shall be considered research carried out on human subjects meeting the definition of section 46.102(f)(2) of title 45, Code of Federal Regulations, for purposes of Federally funded research conducted pursuant to the Public Health Service Act until such time as updates to the Federal Policy for the Protection of Human Subjects (the Common Rule) are promulgated pursuant to subsection (c). For purposes of this subsection, sections 46.116(c) and 46.116(d) of title 45, Code of Federal Regulations, shall not apply.
(b) Effective Date.--Subsection (a) shall apply only to newborn dried blood spots used for purposes of Federally funded research that were collected not earlier than 90 days after the date of enactment of this Act.
(c) Regulations.--Not later than 6 months after the date of enactment of this Act, the Secretary of Health and Human Services shall promulgate proposed regulations related to the updating of the Federal Policy for the Protection of Human Subjects (the Common Rule), particularly with respect to informed consent. Not later than 2 years after such date of enactment, the Secretary shall promulgate final regulations based on such proposed regulations.
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Senate amendment submitted
December 8, 2014
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Senate amendment submitted
December 8, 2014
Senate amendment agreed to: Amendment agreed to in Senate by Unanimous Consent.
December 8, 2014
Senate amendment proposed (on the floor): Amendment SA 3976 proposed by Senator Reid for Senator Paul.(consideration: CR S6395; text: CR S6395)
December 8, 2014
Amendment SA 3976 proposed by Senator Reid for Senator Paul. (consideration: CR S6395; text: CR S6395) To clarify the rules relating to newborn screening research and informed consent.
December 8, 2014
Amendment agreed to in Senate by Unanimous Consent.
December 8, 2014