Agency Information Collection Activities: Submission for OMB Review; Comment Request, 57497-57498 [E9-26831]
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57497
Federal Register / Vol. 74, No. 214 / Friday, November 6, 2009 / Notices
these in the May 2011 Follow-Up). The
2010–2011 TUS–CPS, complemented by
the Follow-Up questionnaire, will be
useful for researchers interested in
measuring the impact on tobacco
cessation of new FDA regulation (the
Family Smoking Prevention and
Tobacco Control Act) as it is
implemented, and will complement
Federal tobacco research and policy
efforts. Frequency of Response: Onetime study for the main 2010–2011
survey; One-time study for the May
2011 Follow-Up. Affected Public:
Individuals or households. Type of
Respondents: Persons 18 years of age or
older. The annualized cost to
respondents is estimated at $285,000.
There are no Capital Costs, Operating
Costs, and/or Maintenance Costs to
report. The annual reporting burden is
presented in the table below.
TABLE—ESTIMATES OF ANNUAL BURDEN HOURS
Number of respondents
(annualized)
Responses
per respondent
May 2010: Individuals ..........................................................................................
August 2010: Individuals .....................................................................................
January 2011: Individuals ....................................................................................
May 2011 Follow-Up: Individuals ........................................................................
30,000
30,000
30,000
15,000
1
1
1
1
Totals ............................................................................................................
105,000
Type of respondent per survey period
mstockstill on DSKH9S0YB1PROD with NOTICES6
Request for Comments: Written
comments and/or suggestions from the
public and affected agencies should
address one or more of the following
points: (1) Evaluate whether the
proposed collection of information is
necessary for the proper performance of
the function of the agency, including
whether the information will have
practical utility; (2) evaluate the
accuracy of the agency’s estimate of the
burden of the proposed collection of
information, including the validity of
the methodology and assumptions used;
(3) enhance the quality, utility and
clarity of the information to be
collected; and (4) minimize the burden
of the collection of information on those
who are to respond, including the use
of appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the data collection plans and
instruments, contact Anne Hartman,
M.S., M.A., Health Statistician, National
Cancer Institute, 6130 Executive Blvd—
MSC 7344, Executive Plaza North, Suite
4005, Bethesda, Maryland 20892–7344,
or call non-toll free 301–496–4970, or
FAX your request, to 301–435–3710, or
e-mail your request, including your
address, to ah42t@nih.gov or
hartmana@mail.nih.gov.
Comments Due Date: Comments
regarding this information collection are
best assured of having their full effect if
received within 60 days of the date of
this publication.
VerDate Nov<24>2008
18:23 Nov 05, 2009
Jkt 220001
Dated: November 2, 2009.
Vivian Horovitch-Kelley,
NCI Project Clearance Liaison, National
Institutes of Health.
[FR Doc. E9–26848 Filed 11–5–09; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS 10198 and CMS–
10296]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
AGENCY: 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
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.
PO 00000
Frm 00051
Fmt 4703
Sfmt 4703
Average time
per response
(minutes/hour)
9/60
9/60
9/60
6/60
(0.15)
(0.15)
(0.15)
(0.10)
Annual burden
hours
4,500
4,500
4,500
1,500
15,000
1. Type of Information Collection
Request: Extension without change of a
currently approved collection; Title of
Information Collection: Creditable
Coverage Disclosure to CMS On-Line
Form and Instructions; Use: Most
entities that currently provide
prescription drug benefits to any
Medicare Part D eligible individual
must disclose to the CMS whether the
prescription drug benefit that they offer
is creditable. The disclosure is required
to be provided annually and upon any
change that affects whether the coverage
is creditable prescription drug coverage.
CMS released a Disclosure to CMS
Guidance Paper and a disclosure to
CMS notification on-line form in
January 2006.
Section 1860D–1 of the Medicare
Prescription Drug, Improvement, and
Modernization Act of 2003 (MMA) and
implementing regulations at 42 CFR
423.56 require that entities that offer
prescription drug benefits under any of
the types of coverage described in 42
CFR 423.56 (b) provide a disclosure of
creditable coverage to CMS informing us
whether such coverage meets the
actuarial requirements specified in
guidelines provided by CMS. Form
Number: CMS–10198 (OMB#: 0938–
1013); Frequency: Reporting—Yearly
and Semi-annually; Affected Public:
Federal Government, Business or other
for-profits and not-for-profit
institutions, and State, Local, or Tribal
Governments; Number of Respondents:
87,500; Total Annual Responses:
87,500; Total Annual Hours: 7,291.7.
(For policy questions regarding this
collection contact Louis Blank at 410–
786–5511. For all other issues call 410–
786–1326.)
2. Type of Information Collection
Request: New collection; Title of
Information Collection: Electronic
E:\FR\FM\06NON1.SGM
06NON1
mstockstill on DSKH9S0YB1PROD with NOTICES6
57498
Federal Register / Vol. 74, No. 214 / Friday, November 6, 2009 / Notices
Health Records (EHR) Testing; Use: The
Centers for Medicare and Medicaid
Services (CMS) has indicated through
statements in proposed and final
rulemaking for the Reporting Hospital
Quality Data for Annual Payment
Update (RHQDAPU) program that it is
actively seeking to pursue quality
measurement based on alternative
sources of data that do not require
manual chart abstraction or that utilize
data already being reported by many
hospitals for other programs, as doing so
would potentially reduce the burden
associated with the collection and
reporting of measures for the program.
Over the years, we have encouraged
hospitals to take steps toward the
adoption of electronic health records
(EHRs) that would allow for reporting of
clinical quality data from the EHRs
directly to a CMS data repository
beginning with the FY 2006 Inpatient
Prospective Payment System (IPPS)
Rule (70 FR 47420 through 47421). We
have also encouraged hospitals that are
implementing, upgrading, or developing
EHR systems to ensure that the
technology obtained, upgraded, or
developed conforms to standards
adopted by the Department of Health
and Human Services (HHS).
In the IPPS 2010 proposed rule (74 FR
24182), we described our intent to begin
a voluntary testing program for the
submission to CMS of standardized data
elements needed to calculate inpatient
hospital quality measures on the topics
of Stroke, Venous Thromboembolism,
and Emergency department throughput.
These measures have not been adopted
for Reporting Hospital Quality for
Annual Payment Update (RHQDAPU)
program, and participation in this
voluntary EHR-testing program will not
substitute for submission of data
elements required under the RHQDAPU
program in a time, form and manner
specified by the Secretary. Similarly,
non-participation in this voluntary
program will not incur any penalties.
The results of this voluntary testing
process will enable CMS to assess the
feasibility of collecting data elements
via electronic health records as a future
alternative to submission of manually
chart abstracted data elements by
hospitals, thereby potentially reducing
the administrative burden associated
with submission of quality measures for
the RHQDAPU program. Form Number:
CMS–10296 (OMB#: 0938–New);
Frequency: Reporting—Once; Affected
Public: Private Sector—Business or
other for-profits and Not-for-profit
institutions; Number of Respondents:
55; Total Annual Responses: 55; Total
Annual Hours: 28,655. (For policy
VerDate Nov<24>2008
18:23 Nov 05, 2009
Jkt 220001
questions regarding this collection
contact Shaheen Halim 410–786–0641.
For all other issues call 410–786–1326.)
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/
PaperworkReductionActof1995, or email 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.
To be assured consideration,
comments and recommendations for the
proposed information collections must
be received by the OMB desk officer at
the address below, no later than 5 p.m.
on December 7, 2009.
OMB, Office of Information and
Regulatory Affairs,
Attention: CMS Desk Officer.
Fax Number: (202) 395–6974.
E-mail:
OIRA_submission@omb.eop.gov.
Dated: October 30, 2009.
Michelle Shortt,
Director, Regulations Development Group,
Office of Strategic Operations and Regulatory
Affairs.
[FR Doc. E9–26831 Filed 11–5–09; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–R–0282]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
AGENCY: 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) 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
PO 00000
Frm 00052
Fmt 4703
Sfmt 4703
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: Medicare
Advantage Appeals and Grievance Data
Disclosure Requirements (42 CFR
422.111); Use: Medicare Advantage
(MA) organizations must disclose
information pertaining to the number of
disputes, and their disposition in the
aggregate, with the categories of
grievances and appeals to any
individual eligible to elect an MA
organization who requests this
information. Medicare demonstrations
also are required to conform to MA
appeals regulations and thus are
included in the count of organizations
affected by this requirement. MA
organizations also are required by the
statute and the MA regulation to
provide aggregate grievance data to MA
eligible beneficiaries upon request. MA
eligible individuals will use this
information to help them make
informed decisions about their
organization’s performance in the area
of appeals and grievances. Form
Number: CMS–R–0282 (OMB#: 0938–
0778); Frequency: Reporting—Semiannually and Yearly; Affected Public:
Business or other for-profits and Notfor-profit institutions; Number of
Respondents: 629; Total Annual
Responses: 47,175; Total Annual Hours:
4,931.36. (For policy questions
regarding this collection contact
Stephanie Simons at 206–615–2420. For
all other issues call 410–786–1326.)
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, access CMS’ Web site
at: https://www.cms.hhs.gov/
PaperworkReductionActof1995, or email 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.
In commenting on the proposed
information collections please reference
the document identifier or OMB control
number. To be assured consideration,
comments and recommendations must
be submitted in one of the following
ways by January 5, 2010:
1. Electronically. You may submit
your comments electronically to https://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) accepting comments.
E:\FR\FM\06NON1.SGM
06NON1
Agencies
[Federal Register Volume 74, Number 214 (Friday, November 6, 2009)]
[Notices]
[Pages 57497-57498]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-26831]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS 10198 and CMS-10296]
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
AGENCY: 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 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 without change
of a currently approved collection; Title of Information Collection:
Creditable Coverage Disclosure to CMS On-Line Form and Instructions;
Use: Most entities that currently provide prescription drug benefits to
any Medicare Part D eligible individual must disclose to the CMS
whether the prescription drug benefit that they offer is creditable.
The disclosure is required to be provided annually and upon any change
that affects whether the coverage is creditable prescription drug
coverage. CMS released a Disclosure to CMS Guidance Paper and a
disclosure to CMS notification on-line form in January 2006.
Section 1860D-1 of the Medicare Prescription Drug, Improvement, and
Modernization Act of 2003 (MMA) and implementing regulations at 42 CFR
423.56 require that entities that offer prescription drug benefits
under any of the types of coverage described in 42 CFR 423.56 (b)
provide a disclosure of creditable coverage to CMS informing us whether
such coverage meets the actuarial requirements specified in guidelines
provided by CMS. Form Number: CMS-10198 (OMB: 0938-1013);
Frequency: Reporting--Yearly and Semi-annually; Affected Public:
Federal Government, Business or other for-profits and not-for-profit
institutions, and State, Local, or Tribal Governments; Number of
Respondents: 87,500; Total Annual Responses: 87,500; Total Annual
Hours: 7,291.7. (For policy questions regarding this collection contact
Louis Blank at 410-786-5511. For all other issues call 410-786-1326.)
2. Type of Information Collection Request: New collection; Title of
Information Collection: Electronic
[[Page 57498]]
Health Records (EHR) Testing; Use: The Centers for Medicare and
Medicaid Services (CMS) has indicated through statements in proposed
and final rulemaking for the Reporting Hospital Quality Data for Annual
Payment Update (RHQDAPU) program that it is actively seeking to pursue
quality measurement based on alternative sources of data that do not
require manual chart abstraction or that utilize data already being
reported by many hospitals for other programs, as doing so would
potentially reduce the burden associated with the collection and
reporting of measures for the program. Over the years, we have
encouraged hospitals to take steps toward the adoption of electronic
health records (EHRs) that would allow for reporting of clinical
quality data from the EHRs directly to a CMS data repository beginning
with the FY 2006 Inpatient Prospective Payment System (IPPS) Rule (70
FR 47420 through 47421). We have also encouraged hospitals that are
implementing, upgrading, or developing EHR systems to ensure that the
technology obtained, upgraded, or developed conforms to standards
adopted by the Department of Health and Human Services (HHS).
In the IPPS 2010 proposed rule (74 FR 24182), we described our
intent to begin a voluntary testing program for the submission to CMS
of standardized data elements needed to calculate inpatient hospital
quality measures on the topics of Stroke, Venous Thromboembolism, and
Emergency department throughput. These measures have not been adopted
for Reporting Hospital Quality for Annual Payment Update (RHQDAPU)
program, and participation in this voluntary EHR-testing program will
not substitute for submission of data elements required under the
RHQDAPU program in a time, form and manner specified by the Secretary.
Similarly, non-participation in this voluntary program will not incur
any penalties. The results of this voluntary testing process will
enable CMS to assess the feasibility of collecting data elements via
electronic health records as a future alternative to submission of
manually chart abstracted data elements by hospitals, thereby
potentially reducing the administrative burden associated with
submission of quality measures for the RHQDAPU program. Form Number:
CMS-10296 (OMB: 0938-New); Frequency: Reporting--Once;
Affected Public: Private Sector--Business or other for-profits and Not-
for-profit institutions; Number of Respondents: 55; Total Annual
Responses: 55; Total Annual Hours: 28,655. (For policy questions
regarding this collection contact Shaheen Halim 410-786-0641. For all
other issues call 410-786-1326.)
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/PaperworkReductionActof1995, 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.
To be assured consideration, comments and recommendations for the
proposed information collections must be received by the OMB desk
officer at the address below, no later than 5 p.m. on December 7, 2009.
OMB, Office of Information and Regulatory Affairs,
Attention: CMS Desk Officer.
Fax Number: (202) 395-6974.
E-mail: OIRA_submission@omb.eop.gov.
Dated: October 30, 2009.
Michelle Shortt,
Director, Regulations Development Group, Office of Strategic Operations
and Regulatory Affairs.
[FR Doc. E9-26831 Filed 11-5-09; 8:45 am]
BILLING CODE 4120-01-P