Emergency Clearance: Public Information Collection Requirements Submitted to the Office of Management and Budget (OMB), 30730-30731 [05-10706]
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30730
Federal Register / Vol. 70, No. 102 / Friday, May 27, 2005 / Notices
Street, NW., Room 4035, Washington,
DC 20405, telephone (202) 208–7312.
Please cite OMB Control No. 3090–0262,
Identification of Products with
Environmental Attributes, in all
correspondence.
Dated: May 20, 2005.
Julia Wise,
Director,Contract Policy Division.
[FR Doc. 05–10610 Filed 5–26–05; 8:45 am]
BILLING CODE 6820–61–S
GENERAL SERVICES
ADMINISTRATION
[OMB Control No. 3090–0027]
General Services Administration
Acquisition Regulation; Information
Collection; Contract Administration,
Quality Assurance (GSAR Parts 542
and 546; GSA Form 1678, DD Form
250, and GSA Form 308)
Office of the Chief Acquisition
Officer, GSA.
ACTION: Notice of request for comments
regarding a renewal to an existing OMB
clearance.
AGENCY:
SUMMARY: Under the provisions of the
Paperwork Reduction Act of 1995 (44
U.S.C. Chapter 35), the General Services
Administration will be submitting to the
Office of Management and Budget
(OMB) a request to review and approve
a renewal of a currently approved
information collection requirement
regarding contract administration, and
quality assurance. A request for public
comments was published at 70 FR 8589,
February 22, 2005. No comments were
received.
Public comments are particularly
invited on: Whether this collection of
information is necessary and whether it
will have practical utility; whether our
estimate of the public burden of this
collection of information is accurate,
and based on valid assumptions and
methodology; ways to enhance the
quality, utility, and clarity of the
information to be collected.
DATES: Submit comments on or before:
June 27, 2005.
FOR FURTHER INFORMATION CONTACT: Ms.
Jeritta Parnell, Procurement Analyst,
Contract Policy Division, at telephone
(202) 501–4082 or via e-mail to
jeritta.parnell@gsa.gov.
ADDRESSES: Submit comments regarding
this burden estimate or any other aspect
of this collection of information,
including suggestions for reducing this
burden to Ms. Jeanette Thornton, GSA
Desk Officer, OMB, Room 10236, NEOB,
Washington, DC 20503, and a copy to
the Regulatory Secretariat (VIR), General
Services Administration, Room 4035,
VerDate jul<14>2003
17:25 May 26, 2005
Jkt 205001
1800 F Street, NW., Washington, DC
20405. Please cite OMB Control No.
3090–0027, Contract Administration,
Quality Assurance (GSAR Parts 542 and
546; GSA Form 1678, DD Form 250, and
GSA Form 308), in all correspondence.
SUPPLEMENTARY INFORMATION:
A. Purpose
Under certain contracts, because of
reliance on contractor inspection in lieu
of Government inspection, GSA’s
Federal Supply Service (FSS) requires
documentation from its contractors to
effectively monitor contractor
performance and ensure that it will be
able to take timely action should that
performance be deficient.
B. Annual Reporting Burden
Respondents: 4,604
Total Responses: 116,869
Total Burden Hours: 7,830
Obtaining Copies of Proposals:
Requesters may obtain a copy of the
information collection documents from
the General Services Administration,
Regulatory Secretariat (VIR), 1800 F
Street, NW., Room 4035, Washington,
DC 20405, telephone (202) 208–7312.
Please cite OMB Control No. 3090–0027,
Contract Administration, Quality
Assurance (GSAR Parts 542 and 546;
GSA Form 1678, DD Form 250, and GSA
Form 308), in all correspondence.
Dated: May 20, 2005.
Julia Wise,
Director,Contract Policy Division
[FR Doc. 05–10611 Filed 5–26–05; 8:45 am]
BILLING CODE 6820–61–S
Times and Dates: 12 p.m.–5:30 p.m., June
15, 2005 (Closed). 8:30 a.m.–5 p.m., June 16,
2005 (Closed). 8:30 a.m.–5 p.m., June 17,
2005 (Closed).
Place: Westin Hotel at Perimeter North, 7
Concourse Parkway, Atlanta, GA 30328,
Telephone Number 770.395.3900.
Status: The meeting will be closed to the
public in accordance with provisions set
forth in Section 552b(c)(4) and (6), Title 5
U.S.C., and the Determination of the Director,
Management Analysis and Services Office,
CDC, pursuant to Public Law 92–463.
Matters to be Discussed: The meeting will
include the review, discussion, and
evaluation of applications received in
response to: Capacity Building Assistance to
Improve the Delivery and Effectiveness of
Human Immunodeficiency Virus (HIV)
Prevention Interventions for High-Risk
Racial/Ethnic Minority Subpopulations,
Program Announcement 05051.
Contact Person for More Information: Beth
Wolfe, Designated Federal Official, National
Center for HIV, STD, and TB Prevention,
CDC, Corporate Square Office Park, 8
Corporate Square Boulevard, Mailstop E07,
Atlanta, GA 30329, Telephone (404) 639–
8531.
The Director, Management Analysis and
Services Office, has been delegated the
authority to sign Federal Register notices
pertaining to announcements of meetings and
other committee management activities, for
both CDC and the Agency for Toxic
Substances and Disease Registry.
Dated: May 23, 2005.
Alvin Hall,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 05–10644 Filed 5–26–05; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
BILLING CODE 4163–18–P
Centers for Disease Control and
Prevention
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Disease, Disability, and Injury
Prevention and Control Special
Emphasis Panel (SEP): Capacity
Building Assistance To Improve the
Delivery and Effectiveness of Human
Immunodeficiency Virus (HIV)
Prevention Interventions for High-Risk
Racial/Ethnic Minority Subpopulations,
Program Announcement 05051
Centers for Medicare and Medicaid
Services
In accordance with Section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), the Centers for Disease
Control and Prevention (CDC)
announces the following meeting:
AGENCY:
Name: Disease, Disability, and Injury
Prevention and Control Special Emphasis
Panel (SEP): Capacity Building Assistance to
Improve the Delivery and Effectiveness of
Human Immunodeficiency Virus (HIV)
Prevention Interventions for High-Risk
Racial/Ethnic Minority Subpopulations,
Program Announcement 05051.
PO 00000
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[Document Identifier: CMS–10158]
Emergency Clearance: Public
Information Collection Requirements
Submitted to the Office of Management
and Budget (OMB)
Center for Medicare and
Medicaid Services.
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Centers for Medicare and Medicaid
Services (CMS), Department of Health
and Human Services, is publishing the
following summary of proposed
collections for public comment.
Interested persons are invited to send
comments regarding this burden
E:\FR\FM\27MYN1.SGM
27MYN1
Federal Register / Vol. 70, No. 102 / Friday, May 27, 2005 / Notices
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 functions;
(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.
We are, however, requesting an
emergency review of the information
collection referenced below. In
compliance with the requirement of
section 3506(c)(2)(A) of the Paperwork
Reduction Act of 1995, we have
submitted to the Office of Management
and Budget (OMB) the following
requirements for emergency review. We
are requesting an emergency review
because the collection of this
information is needed before the
expiration of the normal time limits
under OMB’s regulations at 5 CFR part
1320. This is necessary to ensure
compliance with an initiative of the
Administration. We cannot reasonably
comply with the normal clearance
procedures. The use of normal clearance
procedures is reasonably likely to cause
a statutory deadline to be missed.
This survey will support the required
evaluation of the Medicare Home Health
Independence Demonstration mandated
under Section 702 of the Medicare
Prescription Drug, Improvement, and
Modernization Act of 2003 (MMA).
Section 702 of the MMA requires the
Secretary to collect data on effects of the
demonstration on quality of care,
patient outcomes, and any additional
costs to Medicare. One year after the
project’s termination (currently
projected to be October, 2006), the
Secretary is to submit a report including
recommendations to exempt
permanently and severely disabled
homebound beneficiaries from the
traditional homebound restrictions. The
purpose of this survey is to develop the
information Congress seeks, and to
provide CMS with a sound basis for
making the mandated
recommendations. This survey is
designed to study the health and quality
of life impacts of changing the eligibility
requirement, and to provide descriptive
information about the demonstration’s
target population.
CMS is requesting OMB review and
approval of this collection by June 27,
2005, with a 180-day approval period.
Written comments and recommendation
will be accepted from the public if
VerDate jul<14>2003
16:42 May 26, 2005
Jkt 205001
received by the individuals designated
below by June 27, 2005.
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, access CMS’ Web site
address at https://www.cms.hhs.gov/
regulations/pra or e-mail your request,
including your address, phone number,
OMB number, and CMS document
identifier, to Paperwork@cms.hhs.gov,
or call the Reports Clearance Office on
(410) 786–1326.
Interested persons are invited to send
comments regarding the burden or any
other aspect of these collections of
information requirements. However, as
noted above, comments on these
information collection and
recordkeeping requirements must be
mailed and/or faxed to the designees
referenced below by June 27, 2005:
Centers for Medicare and Medicaid
Services, Office of Strategic
Operations and Regulatory Affairs,
Room C5–13–27, 7500 Security
Boulevard, Baltimore, MD 21244–
1850. Fax Number: (410) 786–0262,
Attn: William N. Parham, III, CMS–
10158; and,
OMB Human Resources and Housing
Branch, Attention: Christopher
Martin, New Executive Office
Building, Room 10235, Washington,
DC 20503.
Dated: May 23, 2005.
Michelle Shortt,
Acting Director, Regulations Development
Group, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 05–10706 Filed 5–25–05; 9:15 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–3144–N]
RIN 0938–ZA49
Medicare Program; Calendar Year 2005
Review of the Appropriateness of
Payment Amounts for New Technology
Intraocular Lenses (NTIOLs) Furnished
by Ambulatory Surgical Centers
(ASCs)
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Notice.
AGENCY:
SUMMARY: This notice solicits interested
parties to submit requests for review of
the appropriateness of the payment
amount for a particular intraocular lens
PO 00000
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30731
furnished by an ambulatory surgical
center.
DATES: Requests for review must be
received at the address provided no
later than 5 pm E.S.T. on June 27, 2005.
ADDRESSES: Mail requests for review
(one original and three copies) to the
Centers for Medicare & Medicaid
Services, Department of Health and
Human Services, Attention: Michael
Lyman, Mailstop C1–09–06, 7500
Security Blvd., Baltimore, Maryland
21244–1850.
FOR FURTHER INFORMATION CONTACT:
Michael Lyman, (410) 786–6938.
SUPPLEMENTARY INFORMATION: On
October 31, 1994, the Social Security
Act Amendments of 1994 (SSAA 1994)
(Pub. L. 103–432) were enacted. Section
141(b)(1) of SSAA 1994 required us to
develop and implement a process under
which interested parties may request a
review of the appropriateness of the
payment amount for intraocular lenses
(IOLs) furnished by ambulatory surgical
centers (ASCs) under section
1833(i)(2)(A)(iii) of the Social Security
Act (the Act) on the basis that those
lenses constitute a class of new
technology intraocular lenses (NTIOLs).
On June 16, 1999, we published a
final rule in the Federal Register
entitled ‘‘Adjustment in Payment
Amounts for New Technology
Intraocular Lenses Furnished by
Ambulatory Surgical Centers’’ (64 FR
32198) which added subpart F to 42
CFR part 416. The June 16, 1999 final
rule established a process for adjusting
payment amounts for NTIOLs furnished
by ambulatory surgical centers (ASCs);
defined the terms relevant to the
process; and established an initial flat
rate payment adjustment of $50 for IOLs
that we determine are NTIOLs. The
payment adjustment applies for a 5-year
period that begins when we recognize a
payment adjustment for the first IOL in
a new class of technology, as explained
below. Any subsequent IOLs with the
same characteristics as the first IOL
recognized for a payment adjustment
will receive the adjustment for the
remainder of the 5-year period
established by the first recognized
NTIOL. After July 16, 2002, we have the
option of changing the $50 adjustment
amount through proposed and final
rulemaking in connection with
ambulatory surgical center services. We
have opted not to change the adjustment
amount for calendar year 2005 (CY 05).
Review Process for Establishing Classes
of New Technology Intraocular Lenses
(NTIOLs)
We will classify an IOL as a NTIOL if
the lens meets the definition of a ‘‘new
E:\FR\FM\27MYN1.SGM
27MYN1
Agencies
[Federal Register Volume 70, Number 102 (Friday, May 27, 2005)]
[Notices]
[Pages 30730-30731]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-10706]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare and Medicaid Services
[Document Identifier: CMS-10158]
Emergency Clearance: Public Information Collection Requirements
Submitted to the Office of Management and Budget (OMB)
AGENCY: Center for Medicare and Medicaid Services.
In compliance with the requirement of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the Centers for Medicare and Medicaid
Services (CMS), Department of Health and Human Services, is publishing
the following summary of proposed collections for public comment.
Interested persons are invited to send comments regarding this burden
[[Page 30731]]
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 functions; (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.
We are, however, requesting an emergency review of the information
collection referenced below. In compliance with the requirement of
section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, we have
submitted to the Office of Management and Budget (OMB) the following
requirements for emergency review. We are requesting an emergency
review because the collection of this information is needed before the
expiration of the normal time limits under OMB's regulations at 5 CFR
part 1320. This is necessary to ensure compliance with an initiative of
the Administration. We cannot reasonably comply with the normal
clearance procedures. The use of normal clearance procedures is
reasonably likely to cause a statutory deadline to be missed.
This survey will support the required evaluation of the Medicare
Home Health Independence Demonstration mandated under Section 702 of
the Medicare Prescription Drug, Improvement, and Modernization Act of
2003 (MMA). Section 702 of the MMA requires the Secretary to collect
data on effects of the demonstration on quality of care, patient
outcomes, and any additional costs to Medicare. One year after the
project's termination (currently projected to be October, 2006), the
Secretary is to submit a report including recommendations to exempt
permanently and severely disabled homebound beneficiaries from the
traditional homebound restrictions. The purpose of this survey is to
develop the information Congress seeks, and to provide CMS with a sound
basis for making the mandated recommendations. This survey is designed
to study the health and quality of life impacts of changing the
eligibility requirement, and to provide descriptive information about
the demonstration's target population.
CMS is requesting OMB review and approval of this collection by
June 27, 2005, with a 180-day approval period. Written comments and
recommendation will be accepted from the public if received by the
individuals designated below by June 27, 2005.
To obtain copies of the supporting statement and any related forms
for the proposed paperwork collections referenced above, access CMS'
Web site address at https://www.cms.hhs.gov/regulations/pra or e-mail
your request, including your address, phone number, OMB number, and CMS
document identifier, to Paperwork@cms.hhs.gov, or call the Reports
Clearance Office on (410) 786-1326.
Interested persons are invited to send comments regarding the
burden or any other aspect of these collections of information
requirements. However, as noted above, comments on these information
collection and recordkeeping requirements must be mailed and/or faxed
to the designees referenced below by June 27, 2005:
Centers for Medicare and Medicaid Services, Office of Strategic
Operations and Regulatory Affairs, Room C5-13-27, 7500 Security
Boulevard, Baltimore, MD 21244-1850. Fax Number: (410) 786-0262, Attn:
William N. Parham, III, CMS-10158; and,
OMB Human Resources and Housing Branch, Attention: Christopher Martin,
New Executive Office Building, Room 10235, Washington, DC 20503.
Dated: May 23, 2005.
Michelle Shortt,
Acting Director, Regulations Development Group, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 05-10706 Filed 5-25-05; 9:15 am]
BILLING CODE 4120-01-P