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HB 2750
Missouri House•Introduced
Summary
HB 2750, which modifies provisions relating to testing performed by the department of health and senior services laboratories, was introduced in the House on Jan 6, 2026 by Rep. Bishop Davidson (R) with 1 co-sponsor. It was referred to Health and Mental Health, and last saw action on Jan 8, 2026: Referred: Health and Mental Health(H).
Record
Text
HB 2750 has 1 co-sponsor.
hb2750/introduced.txtSECOND REGULAR SESSIONHOUSE BILL NO. 2750103RD GENERAL ASSEMBLYINTRODUCED BY REPRESENTATIVE DAVIDSON.4026H.01I JOSEPH ENGLER, Chief ClerkAN ACTTo repeal sections 191.317, 191.331, 191.332, and 191.333, RSMo, and to enact in lieuthereof four new sections relating to testing performed by the department of healthand senior services laboratories.Be it enacted by the General Assembly of the state of Missouri, as follows:Section A. Sections 191.317, 191.331, 191.332, and 191.333, RSMo, are repealed2 and four new sections enacted in lieu thereof, to be known as sections 191.317, 191.331,3 191.332, and 191.333, to read as follows:191.317. 1. All testing results and personal information obtained from any2 individual, or from specimens from any individual, shall be held confidential and be3 considered a confidential medical record, except for such information as the individual,4 parent or guardian consents to be released; but the individual must first be fully informed of5 the scope of the information [requests] requested to be released, of the risks, benefits and6 purposes for such release, and of the identity of those to whom the information will be7 released. Statistical data compiled without reference to the identity of any individual shall not8 be declared confidential. Notwithstanding any other provision of law to the contrary, the9 department may release the results of newborn screening tests to a child's health care10 professional. The department shall destroy the results of newborn screening tests after11 one year from the date the results were finalized.122. The specimen shall be retained for [five years] one year after initial submission to13 the department. After [five years] one year, the specimen shall be destroyed. [Unless14 otherwise directed under this section, a biological specimen may be released for purposes ofEXPLANATION — Matter enclosed in bold-faced brackets [thus] in the above bill is not enacted and isintended to be omitted from the law. Matter in bold-face type in the above bill is proposed language.HB 2750 215 anonymous scientific study. At the time of collection, the parent or legal guardian of the child16 from whom a biological specimen was obtained may direct the department to:17(1) Return a biological specimen that remains after all screening tests have been18 performed;19(2) Destroy a biological specimen in a scientifically acceptable manner after all20 screening tests required under section 191.331 or rule promulgated thereunder have been21 performed; or22(3) Store a biological specimen but not release the biological specimen for23 anonymous scientific study.243. A biological specimen released for anonymous study under this section shall not25 contain information that may be used to determine the identity of the donor.]191.331. 1. Every infant who is born in this state shall be tested for phenylketonuria2 and such other metabolic or genetic diseases as are prescribed by the department if the parent3 or guardian of the infant consented to such testing in the manner provided under4 subsection 4 of this section. The test used by the department shall be dictated by accepted5 medical practice and such tests shall be of the types approved by the department. All6 newborn screening tests [required] for the diseases prescribed by the department shall be7 performed by the department of health and senior services laboratories. The attending8 physician, certified nurse midwife, public health facility, ambulatory surgical center or9 hospital shall assure that appropriate specimens are collected and submitted to the department10 of health and senior services laboratories.112. All physicians, certified nurse midwives, public health nurses and administrators of12 ambulatory surgical centers or hospitals shall report to the department all diagnosed cases of13 phenylketonuria and other metabolic or genetic diseases as designated by the department.14 The department shall prescribe and furnish all necessary reporting forms.153. The department shall develop and institute educational programs concerning16 phenylketonuria and other metabolic and genetic diseases and assist parents, physicians,17 hospitals and public health nurses in the management and basic treatment of these diseases.184. [The provisions of this section shall not apply if the parents of such child object to19 the tests or examinations provided in this section on the grounds that such tests or20 examinations conflict with their religious tenets and practices.] An infant shall not be tested21 in accordance with the provisions of this section unless the parent or guardian of the22 infant consented to such testing as described in this subsection. The following criteria23 shall be required for any consent to be deemed valid:24(1) The consent shall be voluntary and informed and given freely and without25 coercion;26(2) The consent shall be given in writing;HB 2750 327(3) The parent or guardian giving consent shall have the capacity to understand28 the risks and benefits of testing; and29(4) The consent shall be provided before the birth of the infant but not during30 any active labor immediately preceding such birth.315. [As provided in subsection 4 of this section, the parents of any child who fail to32 have such test or examination administered after notice of the requirement for such test or33 examination shall be required to document in writing such refusal.] All physicians, certified34 nurse midwives, public health nurses and administrators of ambulatory surgical centers or35 hospitals seeking the consent of the parent or guardian under subsection 4 of this section36 shall provide to the [parents] parent or [guardians] guardian a written packet of educational37 information developed and supplied by the department of health and senior services38 describing the type of specimen, how it is obtained, the nature of diseases being screened, and39 the consequences of treatment and nontreatment. [The attending physician, certified nurse40 midwife, public health facility, ambulatory surgical center or hospital shall obtain the written41 refusal and make such refusal part of the medical record of the infant.]426. Notwithstanding the provisions of section 192.015 to the contrary, the department43 may, by rule, annually determine and impose a reasonable fee for each newborn screening test44 made in any of its laboratories. The department may collect the fee from any entity or45 individual described in subsection 1 of this section in a form and manner established by the46 department. Such fee shall be considered as a cost payable to such entity by a health care47 third-party payer, including, but not limited to, a health insurer operating pursuant to chapter48 376, a domestic health services corporation or health maintenance organization operating49 pursuant to chapter 354, and a governmental or entitlement program operating pursuant to50 state law. Such fee shall not be considered as part of the internal laboratory costs of the51 persons and entities described in subsection 1 of this section by such health care third-party52 payers. No individual shall be denied screening because of inability to pay. Such fees shall53 be deposited in a separate account in the public health services fund created in section54 192.900, and funds in such account shall be used for the support of the newborn screening55 program and activities related to the screening, diagnosis, and treatment, including special56 dietary products, of persons with metabolic and genetic diseases; and follow-up activities that57 ensure that diagnostic evaluation, treatment and management is available and accessible once58 an at-risk family is identified through initial screening; and for no other purpose. These59 programs may include education in these areas and the development of new programs related60 to these diseases.617. Subject to appropriations provided for formula for the treatment of inherited62 diseases of amino acids and organic acids, the department shall provide such formula to63 persons with inherited diseases of amino acids and organic acids subject to the conditionsHB 2750 464 described in this subsection. State assistance pursuant to this subsection shall be available to65 an applicant only after the applicant has shown that the applicant has exhausted all benefits66 from third-party payers, including, but not limited to, health insurers, domestic health services67 corporations, health maintenance organizations, Medicare, Medicaid and other government68 assistance programs.698. Assistance under subsection 7 of this section shall be provided to the following:70(1) Applicants ages birth to five years old meeting the qualifications under subsection71 7 of this section;72(2) Applicants between the ages of six to eighteen meeting the qualifications under73 subsection 7 of this section and whose family income is below three hundred percent of the74 federal poverty level;75(3) Applicants between the ages of six to eighteen meeting the qualifications under76 subsection 7 of this section and whose family income is at three hundred percent of the77 federal poverty level or above. For these applicants, the department shall establish a sliding78 scale of fees and monthly premiums to be paid in order to receive assistance under subsection79 7 of this section; and80(4) Applicants age nineteen and above meeting the qualifications under subsection 781 of this section and who are eligible under an income-based means test established by the82 department to determine eligibility for the assistance under subsection 7 of this section.839. The department shall have authority over the use, retention, and disposal of84 biological specimens and all related information collected in connection with newborn85 screening tests conducted under subsection 1 of this section. The use of such specimens and86 related information shall only be made for public health purposes and shall comply with all87 applicable provisions of federal law. [The department may charge a reasonable fee for the use88 of such specimens for public health research and preparing and supplying specimens for89 research proposals approved by the department.]191.332. 1. By January 1, 2002, the department of health and senior services shall,2 subject to appropriations, expand the newborn screening [requirements] tests in section3 191.331 to include potentially treatable or manageable disorders, which may include but are4 not limited to cystic fibrosis, galactosemia, biotinidase deficiency, congenital adrenal5 hyperplasia, maple syrup urine disease (MSUD) and other amino acid disorders, glucose-6-6 phosphate dehydrogenase deficiency (G-6-PD), MCAD and other fatty acid oxidation7 disorders, methylmalonic acidemia, propionic acidemia, isovaleric acidemia and glutaric8 acidemia Type I.92. By January 1, 2017, the department of health and senior services shall, subject to10 appropriations, expand the newborn screening [requirements] tests in section 191.331 to11 include severe combined immunodeficiency (SCID), also known as bubble boy disease. TheHB 2750 512 department may increase the fee authorized under subsection 6 of section 191.331 to cover13 any additional costs of the expanded newborn screening [requirements] tests under this14 subsection.153. By January 1, 2019, the department of health and senior services shall, subject to16 appropriations, expand the newborn screening [requirements] tests in section 191.331 to17 include spinal muscular atrophy (SMA) and Hunter syndrome (MPS II). The department may18 increase the fee authorized under subsection 6 of section 191.331 to cover any additional19 costs of the expanded newborn screening [requirements] tests under this subsection. To help20 fund initial costs incurred by the state, the department shall apply for available newborn21 screening grant funding specific to screening for spinal muscular atrophy and Hunter22 syndrome. The department shall have discretion in accepting the terms of such grants.234. The department of health and senior services may promulgate rules to implement24 the provisions of this section. No rule or portion of a rule promulgated pursuant to the25 authority of this section shall become effective unless it has been promulgated pursuant to26 chapter 536.191.333. 1. This section shall be known and may be cited as the "Brady Alan2 Cunningham Newborn Screening Act".32. By July 1, 2012, the department of health and senior services shall expand the4 newborn screening [requirements] tests in section 191.331 to include the following lysosomal5 storage diseases: Krabbe disease, Pompe disease, Gaucher disease, Niemann-Pick disease,6 and Fabry disease. The department may by rule screen for additional lysosomal storage7 disorders when the following occurs:8(1) The registration of the necessary reagents with the federal Food and Drug9 Administration;10(2) The availability of the necessary reagents from the Centers for Disease Control11 and Prevention;12(3) The availability of quality assurance testing methodology for such processes; and13(4) The acquisition and installment by the department of equipment necessary to14 implement the expanded screening tests.153. The department may promulgate rules to implement the provisions of this section.16 Any rule or portion of a rule, as that term is defined in section 536.010, that is created under17 the authority delegated in this section shall become effective only if it complies with and is18 subject to all of the provisions of chapter 536 and, if applicable, section 536.028. This section19 and chapter 536 are nonseverable and if any of the powers vested with the general assembly20 pursuant to chapter 536 to review, to delay the effective date, or to disapprove and annul a21 rule are subsequently held unconstitutional, then the grant of rulemaking authority and any22 rule proposed or adopted after August 28, 2009, shall be invalid and void.HB 2750 6234. The department may increase the fee authorized in subsection 6 of section 191.33124 to cover the additional cost of the expanded newborn screening [test required in] tests under25 this section.✔
Modifies provisions relating to testing performed by the department of health and senior services laboratories
Sponsors
Rep. Bishop Davidson (R) sponsors HB 2750, and 1 member has co-sponsored it.
Committees
HB 2750 went before 1 committee: Health and Mental Health.
History
HB 2750 has taken 4 actions since Jan 6, 2026, the latest on Jan 8, 2026.
| Chamber | Action | |||
|---|---|---|---|---|
Jan 8, 2026 | House | Read Second Time (H) | ||
Jan 8, 2026 | House | Referred: Health and Mental Health(H) | ||
Jan 7, 2026 | House | Read First Time (H) | ||
Jan 6, 2026 | House | Prefiled (H) |
Votes
HB 2750 has not gone to a roll call.
Source: house.mo.gov · legiscan.com