Attachment B1 60 day FRN

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Federal Register / Vol. 77, No. 138 / Wednesday, July 18, 2012 / Notices

Advisory Group can be obtained from
the designated contacts or by accessing
the FACA database that is maintained
by the GSA Committee Management
Secretariat. The Web site for the FACA
database is http://fido.gov/
facadatabase/.
Authority: Executive Order 13544, dated
June 10, 2010, as statutorily mandated under
Section 4001 of the Patient Protection and
Affordable Care Act, Public Law 111–148,
dated March 23, 2010. Authority to continue
the Advisory Group on Prevention, Health
Promotion, and Integrative and Public Health
(hereafter referred to as the ‘‘Advisory
Group’’) is given under Executive Order
13591, dated November 23, 2011. The
Advisory Group on Prevention, Health
Promotion, and Integrative and Public Health
is governed by provisions of the Federal
Advisory Committee Act (FACA), Public Law
92–463, as amended (5 U.S.C. App.), which
sets forth standards for the formation and use
of advisory committees.
Dated: July 13, 2012.
Regina Benjamin,
VADM, USPHS, Surgeon General.
[FR Doc. 2012–17445 Filed 7–17–12; 8:45 am]
BILLING CODE 4150–28–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–12–0556]

Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under

review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
chapter 35). To request a copy of these
requests, call the CDC Reports Clearance
Officer at (404) 639–7570 or send an
email to [email protected]. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC or by fax to (202) 395–5806. Written
comments should be received within 30
days of this notice.
Proposed Project
Assisted Reproductive Technology
(ART) Program Reporting System (0920–
0556, exp. 9/30/2012)—Revision—
National Center for Chronic Disease and
Public Health Promotion (NCDDPHP),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The ART program reporting system is
used to comply with Section 2(a) of
Public Law 102–493 (known as the
Fertility Clinic Success Rate and
Certification Act of 1992 (FCSRCA)), 42
U.S.C. 263a–1(a)). FCSRCA requires
each ART program to annually report to
the Secretary through the CDC
pregnancy success rates achieved by
each ART program, the identity of each
embryo laboratory used by such ART
program, and whether the laboratory is
certified or has applied for certification
under the Act. The reporting system
allows CDC to publish an annual
success rate report to Congress as
specified by the FCSRCA.
CDC requests OMB approval to
continue information collection for
three years. This Revision request

includes an increase in the total
estimated burden hours due to an
increase in the estimated number of
responding clinics and an increase in
the estimated number of responses per
respondent. In addition, this Revision
request describes implementation of a
brief, one-time optional feedback survey
at the end of the data submission for
each reporting year. The feedback
survey will elicit information about
ART reporting system usability as well
as respondents’ perspectives on the
usefulness of the information collection.
Information is collected electronically
through the National ART Surveillance
System (NASS), a web-based interface,
or by electronic submission of NASScompatible files. The NASS includes
information about all ART cycles
initiated by any of the ART programs
practicing in the United States and its
territories. The system also collects
information about the pregnancy
outcome of each cycle as well as a
number of data items deemed important
to explain variability in success rates
across ART programs and individuals.
Respondents are the 484 ART
programs in the United States.
Approximately 440 ART programs are
expected to report an average of 339
ART cycles each. The burden estimate
includes the time for collecting,
validating, and reporting the requested
information. Information is collected on
an annual schedule.
There are no costs to the respondents
other than their time. The total
estimated annualized burden hours are
96,960.

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents

Respondents

Form name

ART Programs ................................................

NASS ..............................................................
Feedback Survey ...........................................

Kimberly S. Lane,
Deputy Director, Office of Science Integrity,
Office of the Associate Director for Science,
Office of the Director, Centers for Disease
Control and Prevention.
[FR Doc. 2012–17459 Filed 7–17–12; 8:45 am]

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–12–0835]

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BILLING CODE 4163–18–P

Proposed Data Collections Submitted
for Public Comment and
Recommendations
In compliance with the requirement
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for
opportunity for public comment on

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440
176

Number of
responses per
respondent
339
1

Average
burden per
response
(in hours)
39/60
2/60

proposed data collection projects, the
Centers for Disease Control and
Prevention (CDC) will publish periodic
summaries of proposed projects. To
request more information on the
proposed projects or to obtain a copy of
the data collection plans and
instruments, call 404–639–7570 and
send comments to Kimberly S. Lane, at
CDC, 1600 Clifton Road, MS–D74,
Atlanta, GA 30333 or send an email to
[email protected].
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance

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Federal Register / Vol. 77, No. 138 / Wednesday, July 18, 2012 / Notices
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. Written comments should
be received within 60 days of this
notice.
Proposed Project
Assessing the Safety Culture of
Underground Coal Mining (0920–0835
Expiration 12/31/2012)—Revision—
National Institute for Occupational
Safety and Health (NIOSH), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
NIOSH, under Public Law 91–596,
Sections 20 and 22 (Section 20–22,
Occupational Safety and Health Act of
1970) has the responsibility to conduct
research relating to innovative methods,
techniques, and approaches dealing
with occupational safety and health
problems.
This research relates to occupational
safety and health problems in the coal
mining industry. In recent years, coal
mining safety has attained national
attention due to highly publicized
disasters. Despite these threats to
worker safety and health, the U.S. relies
on coal mining to meet its electricity
needs. For this reason, the coal mining
industry must continue to find ways to
protect its workers while maintaining
productivity. One way to do so is
through improving the safety culture at
coal mines. In order to achieve this
culture, operators, employees, the
inspectorate, etc. must share a
fundamental commitment to it as a

conclusions with respect to the mine’s
safety culture. The results from these
analyses will be presented in a report
describing the status of the behaviors
important to safety culture at that mine.
Data collection for this project had
previously taken place between the
dates of January 1, 2010 and May 1,
2012. During this time period, safety
culture assessments were conducted at
five underground coal mines, including
one small, two medium, and two large
mines located in the Northern
Appalachian, Central Appalachian,
Southern Appalachian, and Western
coal regions. One of the assessments
was conducted at a unionized mine and
the four other assessments were
conducted at non-union mines. Data
were collected from 274 interview
participants and 1,356 survey
respondents.
From this previous data collection,
some trends are beginning to emerge.
These include safety culture
characteristic differences depending on
the size of the mine and also differences
between union and non-union mines.
However, the sample of participating
mines from the previous data collection
is not sufficient for conclusions to be
drawn regarding these emerging trends.
Therefore, the continuation of data
collection is needed in order to include
additional union mines and small mines
into the study sample.
Upon completion, this project will
provide recommendations for the
enactment of new safety practices or the
enhancement of existing safety practices
across the underground coal mining
industry. This final report will present
a generalized model of a positive safety
culture for underground coal mines that
can be applied at individual mines. In
addition, all study measures and
procedures will be available for mines
to use in the future to evaluate their
own safety cultures. There is no cost to
respondents other than their time.

value. This type of culture is known in
other industries as a ‘‘safety culture.’’
Safety culture can be defined as the
characteristics of the work environment,
such as the norms, rules, and common
understandings that influence
employees’ perceptions of the
importance that the organization places
on safety.
NIOSH requests OMB approval to
collect safety culture data from
underground coal mine employees over
a three-year period to continue the
assessment of the current safety culture
of underground coal mining in order to
identify recommendations for
promoting and ensuring the existence of
a positive safety culture across the
industry. Up to four underground coal
mines will be studied for this
assessment in an attempt to study mines
of different characteristics. Small,
medium, and large unionized as well as
nonunionized mines will be recruited to
diversify the research sample. Data will
be collected one time at each mine; this
is not a longitudinal study. The
assessment includes the collection of
data using several diagnostic tools:
functional analysis, structured
interviews, behavioral observations, and
surveys.
It is estimated that across the four
mines, approximately 1,144 respondents
will be surveyed. The exact number of
interviews conducted will be based
upon the number of individuals in the
mine populations, but it is estimated
that, across the four mines,
approximately 201 interviews will be
conducted. An exact number of
participants is unavailable at this time
because not all mine sites have been
selected.
The use of multiple methods to assess
safety culture is a key aspect to the
methodology. After all of the
information has been gathered, a variety
of statistical and qualitative analyses are
conducted on the data to obtain

ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents

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Underground Coal Mine Employees

Total ...........................................

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Number of
respondents

Form name

Number of
responses per
respondent

Average
burden per
response
(in hours)

Total burden
(in hours)

Safety Culture Survey ......................
Behavioral Anchored Rating Scale
Interview.

1144
201

1
1

20/60
1

381
201

...........................................................

........................

........................

........................

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Federal Register / Vol. 77, No. 138 / Wednesday, July 18, 2012 / Notices

Kimberly S. Lane,
Deputy Director, Office of Science Integrity,
Office of the Associate Director for Science,
Office of the Director, Centers for Disease
Control and Prevention.
[FR Doc. 2012–17456 Filed 7–17–12; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–643 and CMS–
10185]

Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
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: Hospice Survey
and Deficiencies Report Form and
Supporting Regulations. Use: CMS uses
the information collected as the basis for
certification decisions for hospices that
wish to obtain or retain participation in
the Medicare and Medicaid programs.
The information is used by CMS
regional offices, which have the
delegated authority to certify Medicare
facilities for participation, and by State
Medicaid agencies, which have
comparable authority under Medicaid.
The information on the Hospice Survey
and Deficiencies Report Form is coded
for entry into the OSCAR system. The
data is analyzed by the CMS regional
offices and by the CMS central office
components for program evaluation and

tkelley on DSK3SPTVN1PROD with NOTICES

AGENCY:

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monitoring purposes. The information is
also available to the public upon
request. Form Number: CMS–643 (OCN
0938–0379). Frequency: Yearly. Affected
Public: State, Local, or Tribal
Governments. Number of Respondents:
3,644. Total Annual Responses: 1,217.
Total Annual Hours: 1,217. (For policy
questions regarding this collection
contact Kim Roche at 410–786–3524.
For all other issues call 410–786–1326.)
2. Type of Information Collection
Request: Revision of a currently
approved collection;
Title of Information Collection:
Medicare Part D Reporting
Requirements and Supporting
Regulations; Use: Title I of 42 CFR, Part
423, § 423.514, requires each Part D
Sponsor to have an effective procedure
to provide statistics indicating: the cost
of its operations, the patterns of
utilization of its services, the
availability, accessibility, and
acceptability of its services, information
demonstrating it has a fiscally sound
operation and other matters as required
by CMS. In addition, § 423.505 of the
Medicare Prescription Drug,
Improvement, and Modernization Act
(MMA), establishes as a contract
provision that Part D Sponsors must
comply with the reporting requirements
for submitting drug claims and related
information to CMS. Data collected via
Medicare Part D Reporting
Requirements is an integral resource for
oversight, monitoring, compliance and
auditing activities necessary to ensure
quality provision of the Medicare
Prescription Drug Benefit to
beneficiaries. The data collected will be
validated, analyzed, and utilized for
trend reporting.
The revisions for the CY 2013 include
the removal, addition or both of data
elements for the Prompt Payment by
Part D Sponsors, Grievances, Fraud,
Waste, and Abuse Compliance
Programs, and Plan Oversight of Agents
reporting sections; however, these
changes resulted in no changes to the
burden for these sections. In addition,
we added data elements and revised
data elements for the Medication
Therapy Management Programs and the
Coverage Determinations and
Exceptions reporting sections, which
resulted in an increase in burden hours
for both sections. Lastly, we removed
the following reporting sections and
decreased burden estimates associated
with these sections because these data
are no longer necessary for monitoring
through these reporting requirements:
Access to Extended Day Supplies at
Retail Pharmacies; and Pharmacy
Support of E-prescribing. Form Number:
CMS–10185 (OMB#: 0938–0992);

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Frequency: Yearly, Quarterly, SemiAnnually; Affected Public: Private
Sector, business or other for-profit;
Number of Respondents: 3,180; Total
Annual Responses: 48,152; Total
Annual Hours: 76,240. (For policy
questions regarding this collection
contact LaToyia Grant at 410–786–5434.
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 http://www.cms.hhs.gov/
PaperworkReductionActof1995, or
Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
[email protected], 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 August 17, 2012.
OMB, Office of Information and
Regulatory Affairs, Attention: CMS
Desk Officer, Fax Number: (202) 395–
6974, Email:
[email protected].
Dated: July 12, 2012.
Martique Jones,
Director, Regulations Development Group,
Division B, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2012–17380 Filed 7–17–12; 8:45 am]
BILLING CODE 4120–01–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier CMS–2567]

Agency Information Collection
Activities: Proposed Collection;
Comment Request
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

AGENCY:

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