42 U.S. Code § 263a–5 - Publication

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The Secretary, through the Centers for Disease Control, shall not later than 3 years after October 24, 1992, and annually thereafter publish and distribute to the States and the public—
(1)
(A)   [1] pregnancy success rates reported to the Secretary under section 263a–1 (a)(1) of this title and, in the case of an assisted reproductive technology program which failed to report one or more success rates as required under such section, the name of each such program and each pregnancy success rate which the program failed to report, and
(B) from information reported under section 263a–1 (a)(2) of this title—
(i) the identity of each embryo laboratory in a State which has adopted the certification program under such program and whether such laboratory is certified under section 263a–2 of this title,
(ii) the identity of each embryo laboratory in a State which has not adopted such certification program and which has been certified by an accreditation organization approved by the Secretary under section 263a–3 of this title, and
(iii) in the case of an embryo laboratory which is not certified under section 263a–2 of this title or certified by an accreditation organization approved by the Secretary under section 263a–3 of this title, whether the laboratory applied for certification.


[1]  So in original. No par. (2) has been enacted.

Source

(Pub. L. 102–493, § 6,Oct. 24, 1992, 106 Stat. 3151.)
Codification

Section was enacted as part of the Fertility Clinic Success Rate and Certification Act of 1992, and not as part of the Public Health Service Act which comprises this chapter.
Change of Name

Centers for Disease Control changed to Centers for Disease Control and Prevention by Pub. L. 102–531, title III, § 312,Oct. 27, 1992, 106 Stat. 3504.
Effective Date

Section effective upon expiration of 2 years after Oct. 24, 1992, see section 9 ofPub. L. 102–493, set out as a note under section 263a–1 of this title.

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21 CFR - Food and Drugs

21 CFR Part 4 - REGULATION OF COMBINATION PRODUCTS

21 CFR Part 210 - CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL

21 CFR Part 211 - CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS

21 CFR Part 600 - BIOLOGICAL PRODUCTS: GENERAL

21 CFR Part 606 - CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS

21 CFR Part 610 - GENERAL BIOLOGICAL PRODUCTS STANDARDS

21 CFR Part 660 - ADDITIONAL STANDARDS FOR DIAGNOSTIC SUBSTANCES FOR LABORATORY TESTS

42 CFR - Public Health

42 CFR Part 416 - AMBULATORY SURGICAL SERVICES

42 CFR Part 418 - HOSPICE CARE

42 CFR Part 491 - CERTIFICATION OF CERTAIN HEALTH FACILITIES

42 CFR Part 493 - LABORATORY REQUIREMENTS

 

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