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[Federal Register: June 27, 2002 (Volume 67, Number 124)]
[Notices]
[Page 43321-43322]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr27jn02-86]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-02-63]
Proposed Data Collections Submitted for Public Comment and
Recommendations
In compliance with the requirement of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for opportunity for public comment on
proposed data collection projects, the Centers for Disease Control and
Prevention (CDC) will publish periodic summaries of proposed projects.
To
[[Page 43322]]
request more information on the proposed projects or to obtain a copy
of the data collection plans and instruments, call the CDC Reports
Clearance Officer on (404) 498-1210.
Comments are invited on: (a) Whether the proposed collection of
information is necessary for the proper performance of the functions of
the agency, including whether the information shall have practical
utility; (b) the accuracy of the agency's estimate of the burden of the
proposed collection of information; (c) ways to enhance the quality,
utility, and clarity of the information to be collected; and (d) ways
to minimize the burden of the collection of information on respondents,
including through the use of automated collection techniques or other
forms of information technology. Send comments to Anne O'Connor, CDC
Assistant Reports Clearance Officer, 1600 Clifton Road, MS-D24,
Atlanta, GA 30333. Written comments should be received within 60 days
of this notice.
Proposed Project: Assisted Reproductive Technology (ART) Program
Reporting System, (OMB No. 0920-0556)--Extension--National Center for
Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background: Section 2(a) of Pub. L. 102-493 (known as the Fertility
Clinic Success Rate and Certification Act of 1992 (FCSRCA), 42 U.S.C.
263a-1(a)) requires that each assisted reproductive technology (ART)
program shall annually report to the Secretary through the Centers for
Disease Control and Prevention--(1) pregnancy success rates achieved by
such ART program, and (2) the identity of each embryo laboratory used
by such ART program and whether the laboratory is certified or has
applied for such certification under this act.
The Centers for Disease Control and Prevention (CDC) is seeking to
extend approval of a reporting system for Assisted Reproductive
Technology (ART) Program from the Office of Management and Budget
(OMB). This reporting system has been designed in collaboration with
the Society for Assisted Reproductive Technology (SART) to comply with
the requirements of the FCSRCA. The reporting system includes all ART
cycles initiated by any of the approximately 400 ART programs in the
United States, and covers the pregnancy outcome of each cycle, as well
as a number of data items deemed important to explain variability in
success rates across clinics and across individuals. Data is to be
collected through computer software developed by SART in consultation
with CDC.
In developing the definition of pregnancy success rates and the
list of data items to be reported, CDC has consulted with
representatives of SART, the American Society for Reproductive
Medicine, and RESOLVE, the National Infertility Association (a
national, nonprofit consumer organization), as well as a variety of
individuals with expertise and interest in this field. The average
annual cost to the respondent, including data entry labor and fees, is
estimated to be $2,140.
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Number of Average burden/
Respondents Number of responses/ response (in Total burden
respondents respondent hours) (in hours)
----------------------------------------------------------------------------------------------------------------
ART Clinics..................................... 400 220 5/60 7,333
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Total....................................... .............. .............. .............. 7,333
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Dated: June 20, 2002.
Nancy E. Cheal,
Acting Deputy Director for Policy, Planning and Evaluation, Centers for
Disease Control and Prevention.
[FR Doc. 02-16178 Filed 6-26-02; 8:45 am]
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