Emergency Clearance: Public Information Collection Requirements Submitted to the Office of Management and Budget (OMB), 44300-44301 [06-6658]
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44300
Federal Register / Vol. 71, No. 150 / Friday, August 4, 2006 / Notices
Delete item (2) of the functional
statement for the CDC Connects
(CAU12), Office of the Director (CAU1),
Office of Enterprise Communication
(CAU), Office of the Director (CA), and
insert the following: (2) plans and
develops articles about employees and
their work.
Delete item (6) of the functional
statement for the Document
Development Branch (CCED), Education
and Information Division (CCE),
National Institute for Occupational
Safety and Health (CC), and renumber
the remaining items accordingly.
Dated: July 21, 2006.
William H. Gimson,
Chief Operating Officer, Centers for Disease
Control and Prevention (CDC).
[FR Doc. 06–6675 Filed 8–3–06; 8:45 am]
BILLING CODE 4160–18–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare and Medicaid
Services
[Document Identifier: CMS–10206]
Emergency Clearance: Public
Information Collection Requirements
Submitted to the Office of Management
and Budget (OMB)
Centers for Medicare and
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 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
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
gechino on PROD1PC61 with NOTICES
AGENCY:
VerDate Aug<31>2005
22:39 Aug 03, 2006
Jkt 208001
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(a)(2)(ii). This is necessary to
ensure compliance with an initiative of
the Administration. We cannot
reasonably comply with the normal
clearance procedures because of an
unanticipated event, as stated in 5 CFR
1320.13(a)(2)(iii).
Approval of this notice is essential in
order to comply with Section 302(a)(1)
of the MMA that requires the Secretary
to establish and implement quality
standards for suppliers of certain items
to be applied by recognized
independent accreditation
organizations. Suppliers of Durable
Medical Equipment, Prosthetics,
Orthotics and Supplies (DMEPOS) must
comply with the quality standards (and
thus be accredited) to furnish any item
for which payment is made under
Medicare Part B. The DMEPOS
providers and suppliers must be
accredited and obtain a National
Supplier Clearinghouse billing number
in order to participate in the
Competitive Acquisition Program for
DMEPOS. The competitive bidding
process final rule will be published
October 1, 2006. However, there are
over 90,000 providers and suppliers that
need to be accredited before the
implementation of this program by
2009, regardless of whether they submit
bids or do not submit bids. Emergency
clearance is required, given the
complexity of this new requirement and
the fact that the industry cannot proceed
until CMS publishes both the quality
standards along with the approved
requirements for independent
accreditation organizations. Otherwise,
the program is in jeopardy of not
meeting the statutory deadline of full
implementation by 2009.
1. Type of Information Collection
Request: New collection; Title of
Information Collection: Durable Medical
Equipment, Prosthetics, Orthotics, and
Supplies (DMEPOS) Supplier
Accreditation Proposals from
Independent Accrediting Bodies; Use:
Under Section 302 of the Medicare
Prescription Drug, Improvement, and
Modernization Act of 2003 (MMA), the
DMEPOS providers and suppliers must
be accredited and obtain a National
Supplier Clearinghouse billing number
in order to competitively bid. Section
302(a)(1) of the MMA added section
1834(a)(20) to the Act, which requires
the Secretary to establish and
implement quality standards for
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Frm 00047
Fmt 4703
Sfmt 4703
suppliers of certain items, including
consumer service standards, to be
applied by recognized independent
accreditation organizations. Suppliers of
DMEPOS must comply with the quality
standards in order to furnish any item
for which payment is made under Part
B, and to receive and retain a provider
or supplier billing number used to
submit claims for reimbursement for
any such item for which payment may
be made under Medicare. Section
1834(a)(20)(B) of the Act requires the
Secretary, notwithstanding section
1865(b) of the Act, to designate and
approve one or more independent
accreditation organizations to apply the
quality standards to suppliers of
DMEPOS and other items. Independent
accreditation organizations must furnish
the specified information to CMS to
allow themselves the opportunity to
submit proposals to implement and
operate the DMEPOS accreditation
program. The information supplied by
the Independent Accreditation
Organizations will be used to evaluate
the accreditation organization’s ability
to meet CMS’ regulations. Form
Number: CMS–10206 (OMB#: 0938–
NEW); Frequency: Reporting—One-time;
Affected Public: Business or other forprofit and Not-for-profit institutions;
Number of Respondents: 10; Total
Annual Responses: 10; Total Annual
Hours: 200.
CMS is requesting OMB review and
approval of this collection by August 9,
2006, with a 180-day approval period.
Written comments and
recommendations will be considered
from the public if received by the
individuals designated below by August
7, 2006.
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 August 7, 2006:
CMS, Office of Strategic Operations and
Regulatory Affairs, Division of
Regulations Development—B, Attn:
William N. Parham, III, Room C4–26–
E:\FR\FM\04AUN1.SGM
04AUN1
44301
Federal Register / Vol. 71, No. 150 / Friday, August 4, 2006 / Notices
05, 7500 Security Boulevard,
Baltimore, MD 21244–1850; and,
OMB Human Resources and Housing
Branch, Attention: Carolyn Lovett,
New Executive Office Building, Room
10235, Washington, DC 20503, Fax
Number: (202) 395–6974.
Dated: July 26, 2006.
Michelle Shortt,
Director, Regulations Development Group,
Office of Strategic Operations and Regulatory
Affairs.
[FR Doc. 06–6658 Filed 7–31–06; 2:20 pm]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Proposed Collection:
Comment Request
In compliance with the requirement
for opportunity for public comment on
proposed data collection projects
(section 3506(c)(2)(A) of Title 44, United
States Code, as amended by the
Paperwork Reduction Act of 1995, Pub.
L. 104–13), the Health Resources and
Services Administration (HRSA)
publishes periodic summaries of
proposed projects being developed for
submission to the Office of Management
and Budget (OMB) under the Paperwork
Reduction Act of 1995. To request more
information on the proposed project or
to obtain a copy of the data collection
plans and draft instruments, call the
HRSA Reports Clearance Officer on
(301) 443–1129.
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.
Proposed Project: Grants for Hospital
Construction and Modernization—
Federal Right of Recovery and Waiver
of Recovery (42 CFR Part 124, Subpart
H) (OMB No. 0915–0099 Extension)
The regulation known as ‘‘Federal
Right of Recovery and Waiver of
Recovery,’’ provides a means for the
Federal Government to recover grant
funds and a method of calculating
interest when a grant-assisted facility
under Titles VI and XVI of the Public
Health Service Act is sold or leased, or
there is a change in use of the facility.
It also allows for a waiver of the right
of recovery under certain circumstances.
Facilities are required to provide written
notice to the Federal Government when
such a change occurs: and to provide
copies of sales contacts, lease
agreements, estimates of current assets
and liabilities, value of equipment,
expected value of land on the new
owner’s books and remaining
depreciation for all fixed assets involved
in the transactions, and other
information and documents pertinent to
the change of status.
Estimates of annualized burden are as
follows:
Form
Number of
respondents
Responses
per
respondent
Total
responses
Hours per
response
Total burden
hours
Reporting requirements 124,704(b) and 707 ......................
10
1
10
1.25
12.5
Send comments to Susan G. Queen,
Ph.D., HRSA Reports Clearance Officer,
Room 10–33, Parklawn Building, 5600
Fishers Lane, Rockville, MD 20857.
Written comments should be received
within 60 days of this notice.
Dated: July 27, 2006.
Caroline Lewis,
Acting Associate Administrator for
Administration and Financial Management.
[FR Doc. E6–12607 Filed 8–3–06; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HOMELAND
SECURITY
Coast Guard
The CFIVSAC will meet in
conference room 2230–32 of the U.S.
Department of Transportation, 400 7th
Street, SW., Washington, DC 20590. The
World Wide Web site can be found at:
https://www.dot.gov/.
Commercial Fishing Industry Vessel
Safety Advisory Committee
Coast Guard, DHS.
Notice of meeting.
gechino on PROD1PC61 with NOTICES
AGENCY:
FOR FURTHER INFORMATION CONTACT:
The Commercial Fishing
Industry Vessel Safety Advisory
Committee (CFIVSAC) will meet to
discuss various issues relating to vessel
SUMMARY:
VerDate Aug<31>2005
22:39 Aug 03, 2006
The CFIVSAC will meet on
September 12 thru 14, 2006, from 8 a.m.
to 5 p.m. The meeting may close early
if all business has been completed.
Requests to make oral presentations
should reach the Coast Guard on or
before August 11, 2006. Written material
for distribution at the meeting should
reach the Coast Guard on or before
September 1, 2006. Requests to have a
copy of any material distributed to each
member of the committee should reach
the Coast Guard on or before August 25,
2006.
DATES:
ADDRESSES:
[USCG–2006–25484]
ACTION:
safety in the commercial fishing
industry. The meeting is open to the
public.
Jkt 208001
Lieutenant Roberto Trevino, by
telephone at 202–372–1248, fax 202–
372–1917, or e-mail:
RTrevino@comdt.uscg.mil.
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Fmt 4703
Sfmt 4703
SUPPLEMENTARY INFORMATION:
Information about the CFIVSAC, up to
date meeting information, and past
meeting minutes are available at the
following World Wide Web site: https://
www.FishSafe.info.
The CFIVSAC will meet to discuss
various issues relating to vessel safety in
the commercial fishing industry. The
meeting is open to the public. Notice of
the meeting is given under the Federal
Advisory Committee Act, 5 U.S.C.
App. 2.
Agenda of Meeting
Items to be discussed and business to
be conducted include:
(1) Approval of July 2005 meeting
minutes.
(2) Brief by the Executive Secretary on
membership status and term limits.
(3) Brief by the Executive Secretary on
the Coast Guard Authorization Act of
2006, Legislative Change Proposals, and
Aleutian Trade Act Notice to Proposed
Rulemaking update.
(4) Discussion of member
responsibilities and expected support
from the Coast Guard.
(5) Discussion on Risk Identification
procedures, Prevention Through People
E:\FR\FM\04AUN1.SGM
04AUN1
Agencies
[Federal Register Volume 71, Number 150 (Friday, August 4, 2006)]
[Notices]
[Pages 44300-44301]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 06-6658]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare and Medicaid Services
[Document Identifier: CMS-10206]
Emergency Clearance: Public Information Collection Requirements
Submitted to the Office of Management and Budget (OMB)
AGENCY: Centers for Medicare and 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 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
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(a)(2)(ii). This is necessary to ensure compliance with an
initiative of the Administration. We cannot reasonably comply with the
normal clearance procedures because of an unanticipated event, as
stated in 5 CFR 1320.13(a)(2)(iii).
Approval of this notice is essential in order to comply with
Section 302(a)(1) of the MMA that requires the Secretary to establish
and implement quality standards for suppliers of certain items to be
applied by recognized independent accreditation organizations.
Suppliers of Durable Medical Equipment, Prosthetics, Orthotics and
Supplies (DMEPOS) must comply with the quality standards (and thus be
accredited) to furnish any item for which payment is made under
Medicare Part B. The DMEPOS providers and suppliers must be accredited
and obtain a National Supplier Clearinghouse billing number in order to
participate in the Competitive Acquisition Program for DMEPOS. The
competitive bidding process final rule will be published October 1,
2006. However, there are over 90,000 providers and suppliers that need
to be accredited before the implementation of this program by 2009,
regardless of whether they submit bids or do not submit bids. Emergency
clearance is required, given the complexity of this new requirement and
the fact that the industry cannot proceed until CMS publishes both the
quality standards along with the approved requirements for independent
accreditation organizations. Otherwise, the program is in jeopardy of
not meeting the statutory deadline of full implementation by 2009.
1. Type of Information Collection Request: New collection; Title of
Information Collection: Durable Medical Equipment, Prosthetics,
Orthotics, and Supplies (DMEPOS) Supplier Accreditation Proposals from
Independent Accrediting Bodies; Use: Under Section 302 of the Medicare
Prescription Drug, Improvement, and Modernization Act of 2003 (MMA),
the DMEPOS providers and suppliers must be accredited and obtain a
National Supplier Clearinghouse billing number in order to
competitively bid. Section 302(a)(1) of the MMA added section
1834(a)(20) to the Act, which requires the Secretary to establish and
implement quality standards for suppliers of certain items, including
consumer service standards, to be applied by recognized independent
accreditation organizations. Suppliers of DMEPOS must comply with the
quality standards in order to furnish any item for which payment is
made under Part B, and to receive and retain a provider or supplier
billing number used to submit claims for reimbursement for any such
item for which payment may be made under Medicare. Section
1834(a)(20)(B) of the Act requires the Secretary, notwithstanding
section 1865(b) of the Act, to designate and approve one or more
independent accreditation organizations to apply the quality standards
to suppliers of DMEPOS and other items. Independent accreditation
organizations must furnish the specified information to CMS to allow
themselves the opportunity to submit proposals to implement and operate
the DMEPOS accreditation program. The information supplied by the
Independent Accreditation Organizations will be used to evaluate the
accreditation organization's ability to meet CMS' regulations. Form
Number: CMS-10206 (OMB: 0938-NEW); Frequency: Reporting--One-
time; Affected Public: Business or other for-profit and Not-for-profit
institutions; Number of Respondents: 10; Total Annual Responses: 10;
Total Annual Hours: 200.
CMS is requesting OMB review and approval of this collection by
August 9, 2006, with a 180-day approval period. Written comments and
recommendations will be considered from the public if received by the
individuals designated below by August 7, 2006.
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 August 7, 2006:
CMS, Office of Strategic Operations and Regulatory Affairs, Division of
Regulations Development--B, Attn: William N. Parham, III, Room C4-26-
[[Page 44301]]
05, 7500 Security Boulevard, Baltimore, MD 21244-1850; and,
OMB Human Resources and Housing Branch, Attention: Carolyn Lovett, New
Executive Office Building, Room 10235, Washington, DC 20503, Fax
Number: (202) 395-6974.
Dated: July 26, 2006.
Michelle Shortt,
Director, Regulations Development Group, Office of Strategic Operations
and Regulatory Affairs.
[FR Doc. 06-6658 Filed 7-31-06; 2:20 pm]
BILLING CODE 4120-01-P