Agency Forms Undergoing Paperwork Reduction Act Review, 38648 [E6-10621]
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38648
Federal Register / Vol. 71, No. 130 / Friday, July 7, 2006 / Notices
Dated: June 30, 2006.
Joan F. Karr,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E6–10620 Filed 7–6–06; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30 Day–06–05AA]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under
review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
chapter 35). To request a copy of these
requests, call the CDC Reports Clearance
Officer at (404) 639–5960 or send an email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC or by fax to (202) 395–6974. Written
comments should be received within 30
days of this notice.
Proposed Project
Early Hearing Detection and
Intervention Hearing Screening and
Follow-up Survey -New- National
Center on Birth Defects and
Developmental Disabilities (NCBDDD),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The National Center on Birth Defects
and Developmental Disabilities
(NCBDDD) of the Centers for Disease
Control and Prevention promotes the
health of babies, children, and adults
with disabilities. Activities related to
addressing hearing loss (HL) among
newborns and infants are part of
NCBDDD’s mission. HL is a common
birth defect that affects approximately
12,000 infants across the United States
each year, and can result in
developmental delays when left
undetected. As awareness about infant
HL increases, so does the demand for
accurate information about incidence,
rate of screening, referral to care, and
loss to follow-up.
Given the lack of a standardized and
readily accessible source of data, CDC’s
Early Hearing Detection and
Intervention (EHDI) program has
developed a survey to be used annually
for State and Territory EHDI Program
Coordinators that utilizes uniform
definitions to collect aggregate,
standardized EHDI data from states and
territories. This information is
important for helping to ensure infants
and children are receiving
recommended screening and follow-up
services, documenting the occurrence
and etiology of differing degrees of HL
among infants, and determining the
overall impact of infant HL on future
outcomes, such as cognitive
development and family dynamics.
These data will also assist state EHDI
programs with quality improvement
activities and provide information that
will be helpful in assessing the impact
of Federal initiatives. The public will be
able to access this information via CDC’s
EHDI Web site (https://www.cdc.gov/
ncbddd/ehdi/). There are no costs to
respondents other than their time. The
total estimated annualized burden is
209 hours.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Respondents
States Contacted .........................................................................................................................
States Completed ........................................................................................................................
Dated: June 30, 2006.
Joan F. Karr,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E6–10621 Filed 7–6–06; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–216 and CMS
10191]
cprice-sewell on PROD1PC66 with NOTICES
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, HHS.
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Centers for Medicare & Medicaid
Services (CMS), Department of Health
AGENCY:
VerDate Aug<31>2005
15:46 Jul 06, 2006
Jkt 208001
and Human Services, is publishing the
following summary of proposed
collections for public comment.
Interested persons are invited to send
comments regarding this burden
estimate or any other aspect of this
collection of information, including any
of the following subjects: (1) The
necessity and utility of the proposed
information collection for the proper
performance of the Agency’s function;
(2) the accuracy of the estimated
burden; (3) ways to enhance the quality,
utility, and clarity of the information to
be collected; and (4) the use of
automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
1. Type of Information Collection
Request: New Collection.
Title of Information Collection: Organ
Procurement Organization/
Histocompatibility Laboratory
Statement of Reimbursable Cost, Manual
Instructions and Supporting Regulations
Contained in 42 CFR 413.20 and 413.24.
PO 00000
Frm 00051
Fmt 4703
Sfmt 4703
55
50
Number of
responses per
respondent
1
1
Average
burden per
response
(in hrs.)
10/60
4
Use: CMS is requesting reapproval of
Form CMS–216–94 (OMB No.0938–
0102). The current form implements
various provisions of the Social Security
Act, including Section 1881(a) which
provides Medicare coverage for endstage renal disease patients who meet
certain entitlement requirements and
kidney donors. It also implements
Sections 1881(b)(2)(B) and 1861(v)(1)(A)
of the Act to determine the reasonable
costs incurred to furnish treatment for
renal patients and transplant patients.
The reasonable costs of securing and
transporting organs cannot be
determined for the fiscal year until the
Organ Procurement Organization/
Histocompatibility Laboratory files its
cost report (Form CMS–216) at year-end
and costs are verified by the Medicare
fiscal intermediary.
Form Number: CMS–216 (OMB#:
0938–0102).
Frequency: Recordkeeping—Daily,
Reporting—Annually.
E:\FR\FM\07JYN1.SGM
07JYN1
]]>Agencies
[Federal Register Volume 71, Number 130 (Friday, July 7, 2006)]
[Notices]
[Page 38648]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-10621]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30 Day-06-05AA]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) publishes a
list of information collection requests under review by the Office of
Management and Budget (OMB) in compliance with the Paperwork Reduction
Act (44 U.S.C. chapter 35). To request a copy of these requests, call
the CDC Reports Clearance Officer at (404) 639-5960 or send an e-mail
to omb@cdc.gov. Send written comments to CDC Desk Officer, Office of
Management and Budget, Washington, DC or by fax to (202) 395-6974.
Written comments should be received within 30 days of this notice.
Proposed Project
Early Hearing Detection and Intervention Hearing Screening and
Follow-up Survey -New- National Center on Birth Defects and
Developmental Disabilities (NCBDDD), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The National Center on Birth Defects and Developmental Disabilities
(NCBDDD) of the Centers for Disease Control and Prevention promotes the
health of babies, children, and adults with disabilities. Activities
related to addressing hearing loss (HL) among newborns and infants are
part of NCBDDD's mission. HL is a common birth defect that affects
approximately 12,000 infants across the United States each year, and
can result in developmental delays when left undetected. As awareness
about infant HL increases, so does the demand for accurate information
about incidence, rate of screening, referral to care, and loss to
follow-up.
Given the lack of a standardized and readily accessible source of
data, CDC's Early Hearing Detection and Intervention (EHDI) program has
developed a survey to be used annually for State and Territory EHDI
Program Coordinators that utilizes uniform definitions to collect
aggregate, standardized EHDI data from states and territories. This
information is important for helping to ensure infants and children are
receiving recommended screening and follow-up services, documenting the
occurrence and etiology of differing degrees of HL among infants, and
determining the overall impact of infant HL on future outcomes, such as
cognitive development and family dynamics. These data will also assist
state EHDI programs with quality improvement activities and provide
information that will be helpful in assessing the impact of Federal
initiatives. The public will be able to access this information via
CDC's EHDI Web site (https://www.cdc.gov/ncbddd/ehdi/). There are no
costs to respondents other than their time. The total estimated
annualized burden is 209 hours.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per
Respondents respondents responses per response (in
respondent hrs.)
----------------------------------------------------------------------------------------------------------------
States Contacted................................................ 55 1 10/60
States Completed................................................ 50 1 4
----------------------------------------------------------------------------------------------------------------
Dated: June 30, 2006.
Joan F. Karr,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E6-10621 Filed 7-6-06; 8:45 am]
BILLING CODE 4163-18-P
