60 Day FRN

Federal Register / Vol. 80, No. 109 / Monday, June 8, 2015 / Notices
consent order that requires them to
make the deal along with a handful of
other changes. But that is not our role.
There is no legal authority for the
proposition that the Commission can
prophylactically impose remedies
without an underlying violation of the
antitrust laws. And there is no legal
authority to support the view that the
Commission can isolate selected
components of a three-way transaction
to find such a violation. In the absence
of such authority, the appropriate
course is to evaluate the three-way
transaction presented to the agency as a
whole. Because I conclude, as
apparently does the Commission, that
the three-way transaction does not
substantially lessen competition, there
is no competitive harm to correct and
any remedy is unnecessary and
unwarranted.5 Entering into consents is
appropriate only when the transaction
at issue—in this case the three-way
transaction—is likely to substantially
lessen competition. This one does not.
[FR Doc. 2015–13861 Filed 6–5–15; 8:45 am]
BILLING CODE 6750–01–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention

Please note: All public comment should be
submitted through the Federal eRulemaking
portal (Regulations.gov) or by U.S. mail to the
address listed above.

[60Day–15–0856; Docket No. CDC–2015–
0041]

Proposed Data Collection Submitted
for Public Comment and
Recommendations

FOR FURTHER INFORMATION CONTACT:

Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:

The Centers for Disease
Control and Prevention (CDC), as part of
its continuing efforts to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies to take this opportunity to
comment on proposed and/or

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SUMMARY:

5 The Commission points to the HSR Act as
providing the legal basis for the FTC to enter into
consent orders ‘‘to ensure that any competitive
issues with a proposed transaction are addressed
effectively.’’ Statement of the Federal Trade
Commission, supra note 1, at 4 n.7. When a
proposed transaction or set of transactions would
not substantially lessen competition, as is the case
with the three way transaction originally proposed
here, there are no competitive issues with the
proposed transaction to be addressed, and the belief
that a consent order may even further mitigate
concerns regarding the transfer of assets is not
material to our analysis under the Clayton Act. The
HSR Act is not in conflict with the Clayton Act and
does not change this result.

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continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on the proposed revision of
the National Quitline Data Warehouse
(NQDW) information collection. The
NQDW is a repository of information
about callers who have received services
from state quitlines and a quarterly
summary of services provided by each
quitline.
DATES: Written comments must be
received on or before August 7, 2015.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2015–
0041 by any of the following methods:
Federal eRulemaking Portal:
Regulation.gov. Follow the instructions
for submitting comments.
Mail: Leroy A. Richardson,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE., MS–
D74, Atlanta, Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. All relevant comments
received will be posted without change
to Regulations.gov, including any
personal information provided. For
access to the docket to read background
documents or comments received, go to
Regulations.gov.

To

request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact the Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE., MS–D74, Atlanta,
Georgia 30329; phone: 404–639–7570;
Email: [email protected].
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires Federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.

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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; (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; and (e) estimates of capital
or start-up costs and costs of operation,
maintenance, and purchase of services
to provide information. Burden means
the total time, effort, or financial
resources expended by persons to
generate, maintain, retain, disclose or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; to develop,
acquire, install and utilize technology
and systems for the purpose of
collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information; and to
transmit or otherwise disclose the
information.
Proposed Project
National Quitline Data Warehouse
(NQDW) (OMB No. 0920–0856, exp. 10/
31/2015)—Revision—National Center
for Chronic Disease and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Despite the high level of public
knowledge about the adverse effects of
smoking, tobacco use remains the
leading preventable cause of disease and
death in the United States. Smoking
results in approximately 480,000 deaths
annually (USDHHS, 2014). This total
includes approximately 41,000 annual
deaths in nonsmoking U.S. adults
caused by secondhand smoke exposure
(USDHHS, 2014). Although the
prevalence of current smoking among
adults has been decreasing, substantial
disparities in smoking prevalence
continue to exist among individuals of
low socioeconomic status, persons with
mental health and substance abuse
conditions, and certain racial/ethnic
populations, among other groups.
Quitlines are telephone-based tobacco
cessation services that help tobacco
users quit through a variety of services,

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Federal Register / Vol. 80, No. 109 / Monday, June 8, 2015 / Notices

including counseling, medications,
information and self-help materials
(NAQC, 2009). Quitlines are effective,
population-based interventions that
increase successful quitting. Tobacco
cessation quitlines overcome many of
the barriers to in-person tobacco
cessation individual and group
counseling because they are free,
available at the caller’s convenience,
and do not require transportation or
child care. They are also efficient and
cost-effective, in part because they offer
multiple services centrally that often are
unavailable locally. CDC has directly
supported state quitlines since 2004
when CDC and the National Cancer
Institute (NCI) created the National
Network of Tobacco Cessation Quitlines
Initiative to provide greater access to
counseling for tobacco cessation to U.S.
tobacco users. Also, as part of the
Initiative, NCI established a toll-free
national portal number at 1–800–QUIT–
NOW. This portal number automatically
transfers callers to their state quitline.
Quitlines now exist in all U.S. states,
the District of Columbia, Guam, and
Puerto Rico. CDC currently supports the
maintenance and enhancement of state
quitlines as part of the National Tobacco
Control Program, a cooperative
agreement program with the states, and
additional funding designated for
ensuring quitline capacity. One of CDC’s
current goals is to expand quitline
capacity so that all callers to the quitline
during a federal media campaign are
offered at least one coaching call, either
immediately upon calling or by being
re-contacted within two to three days. A
secondary purpose is to continue to
expand the capacity of state tobacco
control programs to implement
evidence-based cessation interventions
and to provide interventions that are
culturally and linguistically appropriate
for populations that experience
disparities.
In 2010, with funding provided by the
American Reinvestment and Recovery
Act (ARRA) of 2009, CDC’s Office on
Smoking and Health (OSH) obtained
approval to collect information through
the National Quitline Data Warehouse
(NQDW; OMB No. 0920–0856). The
NQDW information collection
continued from 2012–2014 using funds
from the Patient Protection and
Affordable Care Act (ACA) and CDC’s
Prevention and Public Health Fund
(PPHF). During its five years in
existence, the NQDW has collected a
quarterly services summary report from
50 states, the District of Columbia,
Guam and Puerto Rico. NQDW has also

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collected de-identified, individual-level
data about tobacco users who have
received services from state quitlines
including caller demographics, tobacco
use behaviors of callers, reasons for
calling the quitline, how callers
reported hearing about the quitline,
what services callers have received from
the quitline, and whether or not callers
were able to make successful quit
attempts after using state quitline
programs.
Information collected by the NQDW
has demonstrated an increase in the
demand for quitline services over time.
Unfortunately, quitlines remain underfunded and under-promoted. According
to CDC’s Best Practices for
Comprehensive Tobacco Control
Programs, currently about 1 percent of
tobacco users receive services from state
quitlines each year, however
approximately 6 to 8 percent of tobacco
users could potentially be reached by
state quitlines if quitlines were
sufficiently funded and promoted.
CDC uses the information collected by
the NQDW for ongoing monitoring and
evaluation related to state quitlines. The
NQDW collects important information
used to monitor and evaluate the impact
of funding for tobacco control programs
and state quitlines as well as other
tobacco programs, policies and
interventions. In addition, data
collected by the NQDW serves an
important role in helping CDC assess
the effectiveness of the Tips From
Former Smokers media campaign. The
‘‘Tips’’ campaign was initiated in 2012
to increase public awareness of the
immediate health damage caused by
smoking and to encourage adult
smokers to quit (www.cdc.gov/tips).
CDC plans to request OMB approval
to continue the NQDW information
collection for three years. All 50 states,
the District of Columbia, Guam, and
Puerto Rico will continue to participate.
Changes to be implemented include:
(1) The Asian Smokers’ Quitline
(ASQ) will participate in the NQDW.
The ASQ will be administered and
operated by a single, national quitline
service provider. This change will allow
CDC to assess state quitline efforts to
expand quitline capacity and service
provision to the tobacco users who
speak Asian languages. The total
number of programs reporting through
the NQDW will increase from 53 to 54.
(2) Five questions will be added to the
NQDW Intake Questionnaire concerning
pregnancy, insurance status, type of
health insurance, mental health, and
language of service. This information
will help CDC and the states tailor

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quitline services to the needs of callers.
In 2014, CDC inquired with states as to
whether their state quitlines are already
collecting information on pregnancy
status, insurance status, and mental
health status and learned that most state
quitlines already collect this
information. However, these questions
are not included in the current NQDW
Intake Questionnaire. Adding these
items to the NQDW Intake
Questionnaire will impose minimal
additional burden on states but will
substantially improve the utility of the
NQDW data to identify use of state
quitlines by key tobacco use
populations. Finally, CDC proposes to
add a question about the language in
which quitline services are provided.
This question would not be a question
posed to callers, but would be recorded
by the quitline service provider.
(3) In 2012, CDC discontinued data
collection for the NQDW Seven-Month
Follow-up Survey. During the three year
period of this Revision request, the
NQDW Seven-Month Follow-up
Questionnaire will be collected, but
only for callers who receive services
through the Asian Smokers’ Quitline.
Should the need arise in the future to
resume collecting seven-month followup data from all callers, an additional
Revision request will be submitted to
OMB.
Participation in the caller intake and
follow-up interviews is voluntary for
quitline callers. The estimated burden is
10 minutes for a complete intake call
conducted with an individual who calls
on their own behalf. The estimated
burden is one minute for a caller who
requests information for someone else,
as these callers complete only a subset
of questions on the intake questionnaire.
The estimated burden per response for
the Seven-Month Follow-Up
Questionnaire is seven minutes.
As a condition of funding, the 54
cooperative agreement awardees are
required to submit a quarterly services
survey. CDC recognizes that awardees
incur additional burden for preparing
and transmitting summary files with
their de-identified caller intake and
follow-up data. This burden is
acknowledged in the instructions for
transmitting the electronic data files.
There is a net decrease in burden,
primarily due to discontinuation of the
Seven-Month Follow-Up Questionnaire
for the majority of callers.
All information will be submitted to
CDC electronically. There are no costs to
respondents other than their time.

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ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents

Average
burden per
response
(in hrs.)

Total
burden
(in hrs.)

Form name

Quitline callers who contact the
quitline for help themselves.
Caller who contacts the quitline on
behalf of someone else.
Quitline caller who received a quitline
service from the Asian Smokers’
quitline.
Tobacco Control Manager or Their
Designee.

NQDW Intake Questionnaire (complete) ..............

509,742

1

10/60

84,957

NQDW Intake Questionnaire (subset) ..................

26,902

1

1/60

448

NQDW 7-Month Follow-Up Questionnaire ............

659

1

7/60

77

Instructions for Submitting NQDW Intake Questionnaire Electronic Data File to CDC.
Instructions for Submitting NQDW 7-Month Follow-up Electronic Data File to CDC.
NQDW Quitline Services Survey ..........................

54
1

4
1

1
1

216
1

54

4

20/60

72

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

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

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

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

85,771

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

Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2015–13849 Filed 6–5–15; 8:45 am]

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 the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.

BILLING CODE 4163–18–P

Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

[FR Doc. 2015–13924 Filed 6–5–15; 8:45 am]

Centers for Disease Control and
Prevention

BILLING CODE 4163–18–P

Disease, Disability, and Injury
Prevention and Control Special
Emphasis Panel (SEP): Initial Review
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 a meeting for the initial
review of applications in response to
Funding Opportunity Announcement
(FOA), CK15–004, Epicenters for the
Prevention of Healthcare Associated
Infections (HAIs)—Cycle II.

mstockstill on DSK4VPTVN1PROD with NOTICES

Number of
responses
per
respondent

Type of respondents

Time and Date: 10:00 a.m.–4:00 p.m., EDT,
July 9, 2015 (Closed).
Place: Teleconference.
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 for Discussion: The meeting will
include the initial review, discussion, and
evaluation of applications received in
response to ‘‘Epicenters for the Prevention of
Healthcare Associated Infections (HAIs)—
Cycle II’’, FOA CK15–004.
Contact Person for More Information:
Gregory Anderson, M.S., M.P.H., Scientific
Review Officer, CDC, 1600 Clifton Road NE.,
Mailstop E60, Atlanta, Georgia 30329–4027,
Telephone: (404) 718–8833.

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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Office for State, Tribal, Local and
Territorial Support
In accordance with Presidential
Executive Order No. 13175, November
6, 2000, and the Presidential
Memorandum of November 5, 2009, and
September 23, 2004, Consultation and
Coordination with Indian Tribal
Governments, CDC/Agency for Toxic
Substances and Disease Registry
(ATSDR), announces the following
meeting and Tribal Consultation
Session:
Name: Tribal Advisory Committee (TAC)
Meeting and 13th Biannual Tribal
Consultation Session.
Times and Dates: 8:00 a.m.–5:00 p.m.,
August 4, 2015 (TAC Meeting); 8:00 a.m.–
5:00 p.m., August 5, 2015 (13th Biannual
Tribal Consultation Session).
Place: The TAC Meeting and Tribal
Consultation Session will be held at the
Northern Quest, 100 North Hayford Road,
Airway Heights, Washington 99001.
Status: The meetings are being hosted by
CDC/ATSDR in-person only and are open to
the public. Attendees must pre-register for

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the event by Friday, July 3, 2015, at the
following link: http://www.cdc.gov/tribal/
meetings.html.
Purpose: The purpose of these recurring
meetings is to advance CDC/ATSDR support
for and collaboration with tribes, and to
improve the health of tribes through,
including but not limited to, assisting in
eliminating the health disparities faced by
Indian tribes, ensuring that access to critical
health and human services and public health
services is maximized to advance or enhance
the social, physical, and economic status of
American Indian/Alaska Native (AI/AN)
people; and promoting health equity for all
AI/AN people and communities. To advance
these goals, CDC/ATSDR conducts
government-to-government consultations
with elected tribal officials or their
authorized representatives. Consultation is
an enhanced form of communication that
emphasizes trust, respect, and shared
responsibility. It is an open and free
exchange of information and opinion among
parties that leads to mutual understanding
and comprehension.
Matters for Discussion: The TAC and CDC
leaders will discuss the following public
health topics: Chronic disease prevention
and health promotion in Indian Country,
CDC’s budget, and CDC’s communication and
engagement with tribes; however, discussion
is not limited to these topics.
During the 13th Biannual Tribal
Consultation Session, tribes and CDC leaders
will engage in a listening session with CDC’s
director and have roundtable discussions
with CDC senior leaders. Tribes will also
have an opportunity to present testimony on
tribal health issues.
Tribal leaders are encouraged to submit
written testimony by July 17, 2015, by mail
to Annabelle Allison, Deputy Associate
Director, Tribal Support Unit, Office for
State, Tribal, Local and Territorial Support
(OSTLTS), Centers for Disease Control and
Prevention, 4770 Buford Highway NE., MS
E–70, Atlanta, Georgia 30341, or by email to
[email protected].
Depending on the time available, it might
be necessary to limit each presenter’s time.
The agenda is subject to change as
priorities dictate.

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