Emergency Clearance: Public Information Collection Requirements Submitted to the Office of Management and Budget (OMB), 69973-69974 [05-22903]
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Federal Register / Vol. 70, No. 222 / Friday, November 18, 2005 / Notices
jobs and tasks by physicochemical
characteristics, leading to an estimation
of dose rather than mass concentrationbased exposure. (c) It has pioneered the
evaluation of the dermal exposure route
in the beryllium sensitization process.
(d) It has developed and improved
genetic research that will contribute to
manufacturer of beryllium in the U.S.
This has allowed us to establish wellcharacterized worker cohorts within the
beryllium industry. (b) It is conducting
industrial hygiene research that should
significantly improve workplace-based
exposure assessment methods. This
research will allow characterization of
the understanding of risk variability in
sensitization and disease, as well as
discerning the underlying mechanisms.
(e) NIOSH has the institutional stability
to continue longitudinal evaluations of
health outcomes in relation to exposure
and genetic risk factors. There is no cost
to respondents other than their time.
ESTIMATES OF ANNUALIZED BURDEN HOURS
Respondents
Number of
respondents
Number of
responses /
respondent
Average
burden/response
(in hours)
Total burden
(in hours)
Former Workers ...............................................................................................
100
1
30/60
50
Dated: November 14, 2005.
Betsey Dunaway,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. 05–22874 Filed 11–17–05; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Notice and Solicitation for Written
Comments on the Draft CDC Health
Protection Research Guide, 2006–2015
Centers for Disease Control and
Prevention/Agency for Toxic Substances
and Disease Registry.
SUMMARY: The U.S. Centers for Disease
Control and Prevention/Agency for
Toxic Substances and Disease Registry
(hereto referred to as CDC) announces
the availability for public comment of
the draft CDC Health Protection
Research Guide, 2006–2015. CDC is
requesting input on this Research Guide
because maximizing the health impact
of public health research can only be
achieved through the collective efforts
of CDC, other Federal agencies, State
and local partners, academic partners,
business partners, non-profit
organizations, professional societies,
and the public. Please provide input on
any aspect of the Research Guide,
including but not limited to:
• Scope and use of the Research
Guide (including whether it has
identified the areas of health protection
research that most need to be addressed
within the next decade);
• Relevance and level of specificity of
the proposed research topics;
• Additions, deletions or
modifications to the proposed research
topics;
• Research Guide development
process; and
• Other improvements to the
Research Guide.
AGENCY:
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15:21 Nov 17, 2005
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The public comment period is 60
days long. Written comments must be
received by close of business on January
15, 2006 at either of the addresses listed
below.
ADDRESSES: The draft CDC Health
Protection Research Guide, 2006–2015
is available for review by visiting the
Internet site, https://
www.rsvpBOOK.com/custom_pages/
50942/index.php, or by contacting
Jamila Rashid, PhD, Senior Health
Scientist, Centers for Disease Control
and Prevention, Office Of Public Health
Research, 1600 Clifton Road, NE., MD
D–72, Atlanta, GA 30333, 404–639–
4621, ResearchGuide@cdc.gov, for a
hard copy. Written comments may be
submitted electronically at the Internet
site or at the email address listed above.
Written comments may also be sent to
the mailing address above.
FOR FURTHER INFORMATION CONTACT:
Additional information about the CDC
Health Protection Research Guide is
available via the Office of Public Health
Research Web site, https://www.cdc.gov/
od/ophr/cdcra.htm or may be obtained
by communicating with the contact
whose name and telephone number is
listed above.
SUPPLEMENTATY INFORMATION: On
January 10, 2005, the Centers for Disease
Control and Prevention launched an
effort to develop its first ever, agencywide CDC Public Health Protection
Research Guide, 2006–2015. The new
Research Guide will address and
support CDC’s Health Protection Goals
(For additional information about the
Goals please see https://www.cdc.gov/
about/goals).
The Research Guide will also provide
overall guidance for CDC’s intramural
and extramural research as well as serve
as an effective planning and
communication tool for CDC’s public
health research.
The public comment period will give
researchers, representatives of CDC’s
DATES:
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key partner organizations and the public
the opportunity to voice their opinions
regarding the CDC Health Protection
Research Guide, 2006–2015 and the
future direction of CDC’s public health
research. The public comment period
will begin on November 18, 2005 and
end on January 15, 2006.
The Chief Science Officer, CDC, has
been delegated the authority to sign
general Federal Register notices for both
the CDC and ATSDR.
Dated: November 9, 2005.
Dixie E. Snider, Jr.,
Chief Science Officer, Centers for Disease
Control and Prevention.
[FR Doc. 05–22719 Filed 11–17–05; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare and Medicaid
Services
[Document Identifier: CMS–10174]
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
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;
AGENCY:
E:\FR\FM\18NON1.SGM
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69974
Federal Register / Vol. 70, No. 222 / Friday, November 18, 2005 / Notices
(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 because the regular
clearance process will exceed the MMA
mandated prescription drug benefit
effective date and thereby result in
public harm to enrolled Medicare
prescription drug beneficiaries.
The Social Security Act as amended
by the Medicare Prescription Drug
Improvement and Modernization Act of
2003 (MMA) mandates that the
prescription drug benefit be available to
beneficiaries on January 1, 2006. The
conditions under which Medicare
Advantage prescription drug plans
(MA–PD), private prescription drug
plans (PDP) and Fallout Plans/Sponsors
receive payment for the Part D drug
benefit upon collection of Prescription
Drug Event (PDE) data are specified in
sections 1860D–15(c)(1)(C), 1860D–
15(d)(2) and 1860D–15(f) of the MMA
and 42 CFR sections 423.322 and
422.310.
1. Type of Information Collection
Request: New Collection; Title of
Information Collection: Collection of
Prescription Drug Data from MA–PD,
PDP and Fallout Plans/Sponsors for
Medicare Part D Payments and
Supporting Regulations in 42 CFR
423.301, 423.322, 423.875, 423.888 and
422.310; Use: The MMA requires
Medicare payment to Medicare
Advantage (MA) organizations, PDP
sponsors, Fallbacks and other plan
sponsors offering coverage of outpatient
prescription drugs under the new
Medicare Part D benefit. The Act
provided four summary mechanisms for
paying plans: Direct subsidies,
subsidized coverage for qualifying lowincome individuals, Federal reinsurance
subsidies and risk corridor payments. In
VerDate Aug<31>2005
15:21 Nov 17, 2005
Jkt 208001
order to make payment in accordance
with these provisions, CMS has
determined to collect a limited set of
data elements for 100 percent of
prescription drug claims or events from
plans offering Part D coverage. The
transmission of the statutorily required
data will be in an electronic format. The
information users will be Pharmacy
Benefit Managers (PBM), third party
administrators and pharmacies and the
PDPs, MA–PDs, Fallbacks and other
plan sponsors that offer coverage of
outpatient prescription drugs under the
new Medicare Part D benefit to
Medicare beneficiaries. The statutorily
required data will be used primarily for
payment, claims validation, quality
monitoring, program integrity and
oversight; Form Number: CMS–10174
(OMB#: 0938–NEW); Frequency:
Monthly, Quarterly and Annually
Affected Public: Business or other forprofit, and Not-for-profit institutions;
Number of Respondents: 455; Total
Annual Responses: 2,418,000,000; Total
Annual Hours: 4,836.
CMS is requesting OMB review and
approval of these collections by
December 19, 2005, with a 180-day
approval period. Written comments and
recommendation will be considered
from the public if received by the
individuals designated below by
December 18, 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 December 18, 2005:
Centers for Medicare and Medicaid
Services, Office of Strategic Operations
and Regulatory Affairs, Room C4–26–05,
7500 Security Boulevard, Baltimore, MD
21244–1850. Fax Number: (410) 786–
5267. Attn: Bonnie L Harkless; and,
OMB Human Resources and Housing
Branch, Attention: Carolyn Lovett,New
Executive Office Building, Room 10235,
Washington, DC 20503.
PO 00000
Frm 00050
Fmt 4703
Sfmt 4703
Dated: November 9, 2005.
Michelle Shortt,
Director, Regulations Development Group,
Office of Strategic Operations and Regulatory
Affairs.
[FR Doc. 05–22903 Filed 11–17–05; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10130, CMS–
10164 and CMS 10156]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services.
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
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: Extension of a currently
approved collection; Title of
Information Collection: Federal Funding
of Emergency Health Services (section
1011): Provider Payment Determination
and Request for section 1011 On-Call
Payments; Form No.: CMS–10130 (OMB
# 0938–0952); Use: Section 1011 of
MMA provides that the Secretary will
establish a process for eligible providers
to request payment. The Secretary must
directly pay hospitals, physicians, and
ambulance providers (including Indian
Health Service, Indian tribe and tribal
organizations) for their otherwise unreimbursed costs of providing services
required by Section 1867 of the Social
Security Act (EMTALA) and related
hospital inpatient, outpatient and
ambulance services. Payments may be
made only for services furnished to
AGENCY:
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]]>Agencies
[Federal Register Volume 70, Number 222 (Friday, November 18, 2005)]
[Notices]
[Pages 69973-69974]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-22903]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare and Medicaid Services
[Document Identifier: CMS-10174]
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
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;
[[Page 69974]]
(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 because the regular clearance process will exceed
the MMA mandated prescription drug benefit effective date and thereby
result in public harm to enrolled Medicare prescription drug
beneficiaries.
The Social Security Act as amended by the Medicare Prescription
Drug Improvement and Modernization Act of 2003 (MMA) mandates that the
prescription drug benefit be available to beneficiaries on January 1,
2006. The conditions under which Medicare Advantage prescription drug
plans (MA-PD), private prescription drug plans (PDP) and Fallout Plans/
Sponsors receive payment for the Part D drug benefit upon collection of
Prescription Drug Event (PDE) data are specified in sections 1860D-
15(c)(1)(C), 1860D-15(d)(2) and 1860D-15(f) of the MMA and 42 CFR
sections 423.322 and 422.310.
1. Type of Information Collection Request: New Collection; Title of
Information Collection: Collection of Prescription Drug Data from MA-
PD, PDP and Fallout Plans/Sponsors for Medicare Part D Payments and
Supporting Regulations in 42 CFR 423.301, 423.322, 423.875, 423.888 and
422.310; Use: The MMA requires Medicare payment to Medicare Advantage
(MA) organizations, PDP sponsors, Fallbacks and other plan sponsors
offering coverage of outpatient prescription drugs under the new
Medicare Part D benefit. The Act provided four summary mechanisms for
paying plans: Direct subsidies, subsidized coverage for qualifying low-
income individuals, Federal reinsurance subsidies and risk corridor
payments. In order to make payment in accordance with these provisions,
CMS has determined to collect a limited set of data elements for 100
percent of prescription drug claims or events from plans offering Part
D coverage. The transmission of the statutorily required data will be
in an electronic format. The information users will be Pharmacy Benefit
Managers (PBM), third party administrators and pharmacies and the PDPs,
MA-PDs, Fallbacks and other plan sponsors that offer coverage of
outpatient prescription drugs under the new Medicare Part D benefit to
Medicare beneficiaries. The statutorily required data will be used
primarily for payment, claims validation, quality monitoring, program
integrity and oversight; Form Number: CMS-10174 (OMB: 0938-
NEW); Frequency: Monthly, Quarterly and Annually Affected Public:
Business or other for-profit, and Not-for-profit institutions; Number
of Respondents: 455; Total Annual Responses: 2,418,000,000; Total
Annual Hours: 4,836.
CMS is requesting OMB review and approval of these collections by
December 19, 2005, with a 180-day approval period. Written comments and
recommendation will be considered from the public if received by the
individuals designated below by December 18, 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 December 18, 2005: Centers for
Medicare and Medicaid Services, Office of Strategic Operations and
Regulatory Affairs, Room C4-26-05, 7500 Security Boulevard, Baltimore,
MD 21244-1850. Fax Number: (410) 786-5267. Attn: Bonnie L Harkless;
and, OMB Human Resources and Housing Branch, Attention: Carolyn
Lovett,New Executive Office Building, Room 10235, Washington, DC 20503.
Dated: November 9, 2005.
Michelle Shortt,
Director, Regulations Development Group, Office of Strategic Operations
and Regulatory Affairs.
[FR Doc. 05-22903 Filed 11-17-05; 8:45 am]
BILLING CODE 4120-01-P
