Emergency Clearance: Public Information Collection Requirements Submitted to the Office of Management and Budget (OMB), 45568-45569 [06-6773]
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45568
Federal Register / Vol. 71, No. 153 / Wednesday, August 9, 2006 / Notices
1. VB Texas, Inc., Houston, Texas; to
become a bank holding company by
acquiring 100 percent of the voting
shares of Community State Bank,
Boling, Texas.
Board of Governors of the Federal Reserve
System, August 3, 2006.
Jennifer J. Johnson,
Secretary of the Board.
[FR Doc. E6–12921 Filed 8–8–06; 8:45 am]
BILLING CODE 6210–01–S
FEDERAL RESERVE SYSTEM
jlentini on PROD1PC65 with NOTICES
Notice of Proposals to Engage in
Permissible Nonbanking Activities or
to Acquire Companies that are
Engaged in Permissible Nonbanking
Activities
The companies listed in this notice
have given notice under section 4 of the
Bank Holding Company Act (12 U.S.C.
1843) (BHC Act) and Regulation Y (12
CFR Part 225) to engage de novo, or to
acquire or control voting securities or
assets of a company, including the
companies listed below, that engages
either directly or through a subsidiary or
other company, in a nonbanking activity
that is listed in § 225.28 of Regulation Y
(12 CFR 225.28) or that the Board has
determined by Order to be closely
related to banking and permissible for
bank holding companies. Unless
otherwise noted, these activities will be
conducted throughout the United States.
Each notice is available for inspection
at the Federal Reserve Bank indicated.
The notice also will be available for
inspection at the offices of the Board of
Governors. Interested persons may
express their views in writing on the
question whether the proposal complies
with the standards of section 4 of the
BHC Act. Additional information on all
bank holding companies may be
obtained from the National Information
Center website at www.ffiec.gov/nic/.
Unless otherwise noted, comments
regarding the applications must be
received at the Reserve Bank indicated
or the offices of the Board of Governors
not later than August 23, 2006.
A. Federal Reserve Bank of New
York (Anne McEwen, Financial
Specialist) 33 Liberty Street, New York,
New York 10045-0001:
1. Westpac Banking Corporation,
Sydney, Australia; to engage de novo
through its subsidiary, Hastings Funds
Management (US), Inc., New York, New
York, in providing investment and
financial advice, pursuant to section
225.28(b)(6) of Regulation Y.
B. Federal Reserve Bank of San
Francisco (Tracy Basinger, Director,
Regional and Community Bank Group)
VerDate Aug<31>2005
19:05 Aug 08, 2006
Jkt 208001
101 Market Street, San Francisco,
California 94105-1579:
1. Belvedere Capital Fund II L.P. and
Belvedere Capital Partners II LLC, both
of San Francisco, California; to acquire
Hometown Commercial Capital, LLC,
Burlingame, California, and thereby
engage in funding commercial real
estate loans through established
warehouse lines and subsequently
securitizing pools through major Wall
Street firms, pursuant to sections
225.28(b)(1) and (b)(2)(ii) of Regulation
Y.
Board of Governors of the Federal Reserve
System, August 3, 2006.
Jennifer J. Johnson,
Secretary of the Board.
[FR Doc. E6–12922 Filed 8–8–06; 8:45 am]
BILLING CODE 6210–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Disease, Disability, and Injury
Prevention and Control Special
Emphasis Panel (SEP): Initiative To
Integrate Clinical Laboratories into
Public Health Testing, Funding
Opportunity Number CDC–PA–HM06–
605
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:
Name: Disease, Disability, and Injury
Prevention and Control Special
Emphasis Panel (SEP): Initiative to
Integrate Clinical Laboratories into
Public Health Testing, Funding
Opportunity Number (FON) CDC–PA–
HM06–605.
Times and Dates: 8:30 a.m.–4:30 p.m.,
August 3, 2006 (Closed).
8:30 a.m.–4 p.m., August 4, 2006
(Closed).
Place: Centers for Disease Control and
Prevention, Building 19, Conference
Room 256, 1600 Clifton Road, Atlanta,
GA 30333, Telephone 404.498.2329.
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 FON CDC–PA–HM06–605,
‘‘Initiative to Integrate Clinical
PO 00000
Frm 00053
Fmt 4703
Sfmt 4703
Laboratories into Public Health
Testing.’’
Due to programmatic matters, this
Federal Register Notice is being
published on less than 15 calendar days
notice to the public (41 CFR 102–
3.150(b)).
Contact Person for More Information:
Jack Rogers, Ph.D., Program Analyst,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE., MS
E–21, Atlanta, GA 30333, Telephone
404.498.2329.
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: August 3, 2006.
Alvin Hall,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 06–6802 Filed 8–8–06; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare and Medicaid
Services
[Document Identifier: CMS–10207]
Emergency Clearance: Public
Information Collection Requirements
Submitted to the Office of Management
and Budget (OMB)
Center 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.
AGENCY:
E:\FR\FM\09AUN1.SGM
09AUN1
jlentini on PROD1PC65 with NOTICES
Federal Register / Vol. 71, No. 153 / Wednesday, August 9, 2006 / Notices
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).
The Centers for Medicare & Medicaid
Services (CMS) is submitting an
emergency information collection
request for the approval of the
information collection requirements
associated with two new exceptions to
section 1877 of the Social Security Act
(the Act). The approval of this collection
process is essential to protect the
Medicare program and its beneficiaries
against fraud and abuse. In addition,
emergency approval is essential to
permit members of the health care
industry to immediately reap the
benefits of this important regulation.
Once the new exceptions are effective,
entities that furnish certain designated
health services to Medicare beneficiaries
will be permitted to assist physicians
with the implementation of electronic
prescribing and electronic health
records technology. The benefits of this
technology include reducing medical
errors, coordinating care, improving
efficiency, and decreasing health care
costs by eliminating unnecessary and/or
duplicative diagnostic services.
1. Type of Information Collection
Request: New collection; Title of
Information Collection: Physician SelfReferral Exceptions for Electronic
Prescribing and Electronic Health
Records; Use: Section 101 of the
Medicare Prescription Drug,
Improvement, and Modernization Act of
2003 (MMA), directs the Secretary of the
Department of Health and Human
Services (‘‘HHS’’) to create an exception
to the physician self-referral prohibition
in section 1877 of the Social Security
Act (the Act) for certain arrangements in
which a physician receives
compensation in the form of items or
services (not including cash or cash
equivalents) (‘‘nonmonetary
remuneration’’) that is necessary and
used solely to receive and transmit
electronic prescription information. In
VerDate Aug<31>2005
19:05 Aug 08, 2006
Jkt 208001
addition, using our separate legal
authority under section 1877(b)(4) of the
Act, this rule creates a separate
regulatory exception for certain
arrangements involving the provision of
nonmonetary remuneration in the form
of electronic health records software or
information technology and training
services necessary and used
predominantly to create, maintain,
transmit, and receive electronic health
records.
The conditions for both exceptions
require that arrangements for the items
and services provided must be set forth
in a written agreement, signed by the
involved parties, specify the items or
services being provided and the value of
those items or services, and cover all of
the electronic health records technology
to be furnished by the entity. We have
suggested that instead of one master
contract that is updated with each new
donation, the parties may choose to
create a specific new contract and then
reference other agreements or crossreference a master list.
The requirements associated with
these exceptions are limited to
donations made to physicians by
providers, members of integrated
delivery systems, Federally Qualified
Health Centers, or rural health clinics
(for purposes of this Collection of
Information Requirement, ‘‘Providers’’);
by group practices to their physician
members, and by Prescription Drug Plan
(PDPs) sponsors and Medicare
Advantage (MA) organizations to
prescribing physicians. The paperwork
burden is the creation of the written
contracts. The burden associated with
the written agreement requirement is
the time and effort necessary for
documentation of the agreement
between the parties, including
signatures of the parties. Form Number:
CMS–10207 (OMB#: 0938–NEW);
Frequency: Recordkeeping and
Reporting—On occasion; Affected
Public: Business or other for-profit and
Not-for-profit institutions; Number of
Respondents: 87,230; Total Annual
Responses: 87,080; Total Annual Hours:
50,731.
CMS is requesting OMB review and
approval of this collection by September
22, 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
September 18, 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,
PO 00000
Frm 00054
Fmt 4703
Sfmt 4703
45569
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 September 18,
2006: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development—
B, Attn: William N. Parham, III, Room
C4–26–05, 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: August 2, 2006.
Michelle Shortt,
Director, Regulations Development Group,
Office of Strategic Operations and Regulatory
Affairs.
[FR Doc. 06–6773 Filed 8–3–06; 4:04 pm]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 2006N–0219]
Antiviral Drugs Advisory Committee;
Notice of Meeting
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
This notice announces a forthcoming
meeting of a public advisory committee
of the Food and Drug Administration
(FDA). At least one portion of the
meeting will be closed to the public.
Name of Committee: Antiviral Drugs
Advisory Committee.
General Function of the Committee:
To provide advice and
recommendations to the agency on
FDA’s regulatory issues.
Date and Time: The meeting will be
held on October 19, 2006, from 8 a.m.
to 4 p.m. and on October 20, 2006, from
8 a.m. to 4 p.m.
Addresses: Electronic comments
should be submitted to https://
www.fda.gov/dockets/ecomments.
Select ‘‘2006N–0219—Clinical Trial
Design Issues in the Development of
Products for Treatment of Chronic
Hepatitis C’’ and follow the prompts to
E:\FR\FM\09AUN1.SGM
09AUN1
Agencies
[Federal Register Volume 71, Number 153 (Wednesday, August 9, 2006)]
[Notices]
[Pages 45568-45569]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 06-6773]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare and Medicaid Services
[Document Identifier: CMS-10207]
Emergency Clearance: Public Information Collection Requirements
Submitted to the Office of Management and Budget (OMB)
AGENCY: Center 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.
[[Page 45569]]
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).
The Centers for Medicare & Medicaid Services (CMS) is submitting an
emergency information collection request for the approval of the
information collection requirements associated with two new exceptions
to section 1877 of the Social Security Act (the Act). The approval of
this collection process is essential to protect the Medicare program
and its beneficiaries against fraud and abuse. In addition, emergency
approval is essential to permit members of the health care industry to
immediately reap the benefits of this important regulation. Once the
new exceptions are effective, entities that furnish certain designated
health services to Medicare beneficiaries will be permitted to assist
physicians with the implementation of electronic prescribing and
electronic health records technology. The benefits of this technology
include reducing medical errors, coordinating care, improving
efficiency, and decreasing health care costs by eliminating unnecessary
and/or duplicative diagnostic services.
1. Type of Information Collection Request: New collection; Title of
Information Collection: Physician Self-Referral Exceptions for
Electronic Prescribing and Electronic Health Records; Use: Section 101
of the Medicare Prescription Drug, Improvement, and Modernization Act
of 2003 (MMA), directs the Secretary of the Department of Health and
Human Services (``HHS'') to create an exception to the physician self-
referral prohibition in section 1877 of the Social Security Act (the
Act) for certain arrangements in which a physician receives
compensation in the form of items or services (not including cash or
cash equivalents) (``nonmonetary remuneration'') that is necessary and
used solely to receive and transmit electronic prescription
information. In addition, using our separate legal authority under
section 1877(b)(4) of the Act, this rule creates a separate regulatory
exception for certain arrangements involving the provision of
nonmonetary remuneration in the form of electronic health records
software or information technology and training services necessary and
used predominantly to create, maintain, transmit, and receive
electronic health records.
The conditions for both exceptions require that arrangements for
the items and services provided must be set forth in a written
agreement, signed by the involved parties, specify the items or
services being provided and the value of those items or services, and
cover all of the electronic health records technology to be furnished
by the entity. We have suggested that instead of one master contract
that is updated with each new donation, the parties may choose to
create a specific new contract and then reference other agreements or
cross-reference a master list.
The requirements associated with these exceptions are limited to
donations made to physicians by providers, members of integrated
delivery systems, Federally Qualified Health Centers, or rural health
clinics (for purposes of this Collection of Information Requirement,
``Providers''); by group practices to their physician members, and by
Prescription Drug Plan (PDPs) sponsors and Medicare Advantage (MA)
organizations to prescribing physicians. The paperwork burden is the
creation of the written contracts. The burden associated with the
written agreement requirement is the time and effort necessary for
documentation of the agreement between the parties, including
signatures of the parties. Form Number: CMS-10207 (OMB: 0938-
NEW); Frequency: Recordkeeping and Reporting--On occasion; Affected
Public: Business or other for-profit and Not-for-profit institutions;
Number of Respondents: 87,230; Total Annual Responses: 87,080; Total
Annual Hours: 50,731.
CMS is requesting OMB review and approval of this collection by
September 22, 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 September 18, 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 September 18, 2006: CMS, Office of
Strategic Operations and Regulatory Affairs, Division of Regulations
Development--B, Attn: William N. Parham, III, Room C4-26-05, 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: August 2, 2006.
Michelle Shortt,
Director, Regulations Development Group, Office of Strategic Operations
and Regulatory Affairs.
[FR Doc. 06-6773 Filed 8-3-06; 4:04 pm]
BILLING CODE 4120-01-P