Agency Information Collection Activities; Proposed Collection; Public Comment Request, 15725-15726 [2013-05609]
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mstockstill on DSK4VPTVN1PROD with NOTICES
Federal Register / Vol. 78, No. 48 / Tuesday, March 12, 2013 / Notices
mobile devices, awareness and use of
content labeling and rating systems, and
awareness and use of parental controls
for mobile content. Similar questions
will be posed to the adult respondents’
children.
Likely Respondents: With the
assistance of a consumer research firm
(hereafter the Contractor), the FTC will
develop a draft questionnaire for use in
a nationally representative online
survey of parents and (with parental
permission) their children ages 8–16
years who watch movies, listen to
music, and/or play game apps on a
mobile device that runs either the Apple
iOS or Android operating system. To the
extent feasible, the adult panel shall
consist of 100 adult respondents for
each of the nine child age groups
between ages 8 and 16, inclusive (900
total adult respondents). The child
survey shall be conducted as an adjunct
to the parents’ survey, i.e., by surveying
each child about whom the adult
respondents answered their survey
questions (900 total child respondents).
Estimated Annual Hours Burden:
Approximately 417 hours (117 hours for
the adult screener + 300 hours for the
parent and child surveys).
• Screening Questions: The screening
questions will be asked of
approximately 7,000 adult respondents
to provide a large enough random
sample for the surveys. Cumulatively,
screening should require a maximum of
117 hours (7,000 total respondents × 1
minute for each). Because the adult
respondents will be pre-screening the
900 child respondents, the Commission
does not anticipate any burden on
children related to screening.
• Survey Questions: Answering the
surveys will impose a burden per adult
respondent of approximately 10
minutes, totaling 150 hours for all
respondents to the surveys (900
respondents × 10 minutes per survey).
Similarly, answering the surveys will
impose a burden per child respondent
of approximately 10 minutes, totaling
150 hours for all respondents to the
surveys (900 respondents × 10 minutes
per survey).
Estimated annual cost burden: $0.
The cost per respondent should be
negligible. Participation is voluntary,
and will not require any labor
expenditures by respondents. There are
no capital, start-up, operation,
maintenance, or other similar costs to
the respondents.
Request for Comment: You can file a
comment online or on paper. For the
Commission to consider your comment,
we must receive it on or before April 11,
2013. Write ‘‘Entertainment Industry
Study: FTC File No. P994511’’ on your
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17:21 Mar 11, 2013
Jkt 229001
comment. Your comment—including
your name and your state—will be
placed on the public record of this
proceeding, including, to the extent
practicable, on the public Commission
Web site, at https://www.ftc.gov/os/
publiccomments.shtm. As a matter of
discretion, the Commission tries to
remove individuals’ home contact
information from comments before
placing them on the Commission Web
site.
Because your comment will be made
public, you are solely responsible for
making sure that your comment does
not include any sensitive personal
information, like anyone’s Social
Security number, date of birth, driver’s
license number or other state
identification number or foreign country
equivalent, passport number, financial
account number, or credit or debit card
number. You are also solely responsible
for making sure that your comment does
not include any sensitive health
information, like medical records or
other individually identifiable health
information. In addition, do not include
any ‘‘[t]rade secret or any commercial or
financial information * * * which is
privileged or confidential.’’ See Section
6(f) of the FTC Act, 15 U.S.C. 46(f), and
FTC Rule 4.10(a)(2), 16 CFR 4.10(a)(2).
In particular, do not include
competitively sensitive information
such as costs, sales statistics,
inventories, formulas, patterns, devices,
manufacturing processes, or customer
names.
If you want the Commission to give
your comment confidential treatment,
you must file it in paper form, with a
request for confidential treatment, and
you have to follow the procedure
explained in FTC Rule 4.9(c), 16 CFR
4.9(c). Your comment will be kept
confidential only if the FTC General
Counsel, in his or her sole discretion,
grants your request in accordance with
the law and the public interest.
Postal mail addressed to the
Commission is subject to delay due to
heightened security screening. As a
result, we encourage you to submit your
comments online, or to send them to the
Commission by courier or overnight
service. To make sure that the
Commission considers your online
comment, you must file it at https://
ftcpublic.commentworks.com/ftc/
mobileappssurveypra2, by following the
instructions on the web-based form. If
this Notice appears at https://
www.regulations.gov, you also may file
a comment through that Web site.
If you file your comment on paper,
write ‘‘Entertainment Industry Study:
FTC File No. P994511’’ on your
comment and on the envelope, and mail
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15725
or deliver it to the following address:
Federal Trade Commission, Office of the
Secretary, Room H–113 (Annex J), 600
Pennsylvania Avenue NW., Washington,
DC 20580. If possible, submit your
paper comment to the Commission by
courier or overnight service.
Visit the Commission Web site at
https://www.ftc.gov to read this Notice.
The FTC Act and other laws that the
Commission administers permit the
collection of public comments to
consider and use in this proceeding as
appropriate. The Commission will
consider all timely and responsive
public comments that it receives on or
before April 11, 2013. You can find
more information, including routine
uses permitted by the Privacy Act, in
the Commission’s privacy policy, at
https://www.ftc.gov/ftc/privacy.shtm.
Comments on the information
collection requirements subject to
review under the PRA should also be
submitted to OMB. If sent by U.S. mail,
address comments to: Office of
Information and Regulatory Affairs,
Office of Management and Budget,
Attention: Desk Officer for the Federal
Trade Commission, New Executive
Office Building, Docket Library, Room
10102, 725 17th Street NW.,
Washington, DC 20503. Comments sent
to OMB by U.S. postal mail, however,
are subject to delays due to heightened
security precautions. Thus, comments
instead should be sent by facsimile to
(202) 395–5167.
David C. Shonka,
Acting General Counsel.
[FR Doc. 2013–05630 Filed 3–11–13; 8:45 am]
BILLING CODE 6750–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
[Document Identifier: OS–19060–60D]
Agency Information Collection
Activities; Proposed Collection; Public
Comment Request
Office of the Secretary, HHS.
Notice.
AGENCY:
ACTION:
In compliance with section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the Office of the
Secretary(OS), Department of Health
and Human Services, announces plans
to submit a new Information Collection
Request (ICR), described below, to the
Office of Management and Budget
(OMB). Prior to submitting that ICR to
OMB, OS seeks comments from the
SUMMARY:
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15726
Federal Register / Vol. 78, No. 48 / Tuesday, March 12, 2013 / Notices
public regarding the burden estimate,
below, or any other aspect of the ICR.
Comments on the ICR must be
received on or before May 13, 2013.
DATES:
Submit your comments to
Information.CollectionClearance@
hhs.gov or by calling (202) 690–6162.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Information Collection Clearance staff,
Information.CollectionClearance@
hhs.gov or (202) 690–6162.
When
submitting comments or requesting
information, please include the
document identifier HHS–OS–19060–
60D for reference.
SUPPLEMENTARY INFORMATION:
women forty years and over. Evaluation
of the initiative will address the
following questions: (1) Does a healthy
weight intervention based on the
individual and the social environment
improve health and reduce weight of
older lesbian and bisexual women; and,
(2) If the intervention does improve
health and/or reduce weight, what
attributes of the intervention
contributed to this success? Information
will be gathered and analyzed in an
effort to identify and understand the
effects of this healthy weight
intervention and to inform the
applicability of the intervention to other
sites across the United States. The
project is scheduled for one year.
Information Collection Request Title:
Living Healthier, Living Longer Program
Evaluation.
Abstract: The Department of Health
and Human Services (HHS), the Office
of Women’s Health, (OWH)
Coordinating Committee on Lesbian,
Gay, Bi-sexual and Transgender (LGBT)
Issues has prioritized the collection of
health data on LGBT populations. In
response, OWH funded an initiative to
‘‘identify and test effective and
innovative ways of reducing obesity in
lesbian and bisexual women’’ (HHS,
2012). This initiative will include
nutritional and physical activity
counseling and activities, and will be
implemented in New York City. It will
be tailored to bisexual and lesbian
TOTAL ESTIMATED ANNUALIZED BURDEN HOURS
Average
burden per
response
(in hours)
Number of
responses per
respondent
Number of
respondents
Form name
Total burden
hours
Baseline Survey ...............................................................................................
Study Completion Survey ................................................................................
Pedometer Profile ............................................................................................
Health Screen (physical measurement) ..........................................................
Health History Questionnaire ...........................................................................
Intervention Experience Study Mid-Point) .......................................................
Intervention Experience ( Study Completion) ..................................................
40
40
40
40
40
40
40
1
1
1
3
1
1
1
15/60
15/60
2/60
10/60
12/60
1
1
10
10
1
20
8
40 hours
40 hours
Total ..........................................................................................................
........................
........................
........................
129 hours
OS specifically requests comments on
(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.
Keith A. Tucker,
Information Collection Clearance Officer.
[FR Doc. 2013–05609 Filed 3–11–13; 8:45 am]
BILLING CODE 4150–33–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
mstockstill on DSK4VPTVN1PROD with NOTICES
Food and Drug Administration
[Docket No. FDA–2013–N–0001]
Cellular, Tissue and Gene Therapies
Advisory Committee; Notice of Meeting
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
VerDate Mar<15>2010
17:21 Mar 11, 2013
Jkt 229001
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: Cellular, Tissue
and Gene Therapies 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 by teleconference on April 17,
2013, from 1:30 p.m. to 5 p.m.
Location: Rockwall II Building, 5515
Security Lane, Conference Room 1033,
Rockville, MD 20852. The public is
welcome to attend the meeting at the
specified location where a
speakerphone will be provided. Public
participation in the meeting is limited to
the use of the speakerphone in the
conference room.
Contact Person: Gail Dapolito (301–
827–1289) or Rosanna Harvey (301–
827–1297), Food and Drug
Administration, 1401 Rockville Pike
(HFM–71), Rockville, MD 20852, or
FDA Advisory Committee Information
Line, 1–800–741–8138 (301–443–0572
in the Washington, DC area). A notice in
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the Federal Register about last minute
modifications that impact a previously
announced advisory committee meeting
cannot always be published quickly
enough to provide timely notice.
Therefore, you should always check the
Agency’s Web site at https://www.fda.
gov/AdvisoryCommittees/default.htm
and scroll down to the appropriate
advisory committee meeting link, or call
the advisory committee information line
to learn about possible modifications
before coming to the meeting.
Agenda: On April 17, 2013, the
committee will meet by teleconference.
In open session, the committee will hear
updates of research programs in the
Laboratory of Chemistry, Division of
Therapeutic Proteins, Office of
Biotechnology Products, Center for Drug
Evaluation and Research, FDA.
FDA intends to make background
material available to the public no later
than 2 business days before the meeting.
If FDA is unable to post the background
material on its Web site prior to the
meeting, the background material will
be made publicly available at the
location of the advisory committee
meeting, and the background material
will be posted on FDA’s Web site after
the meeting. Background material is
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]]>Agencies
[Federal Register Volume 78, Number 48 (Tuesday, March 12, 2013)]
[Notices]
[Pages 15725-15726]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-05609]
=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the Secretary
[Document Identifier: OS-19060-60D]
Agency Information Collection Activities; Proposed Collection;
Public Comment Request
AGENCY: Office of the Secretary, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with section 3506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the Office of the Secretary(OS), Department of
Health and Human Services, announces plans to submit a new Information
Collection Request (ICR), described below, to the Office of Management
and Budget (OMB). Prior to submitting that ICR to OMB, OS seeks
comments from the
[[Page 15726]]
public regarding the burden estimate, below, or any other aspect of the
ICR.
DATES: Comments on the ICR must be received on or before May 13, 2013.
ADDRESSES: Submit your comments to
Information.CollectionClearance@hhs.gov or by calling (202) 690-6162.
FOR FURTHER INFORMATION CONTACT: Information Collection Clearance
staff, Information.CollectionClearance@hhs.gov or (202) 690-6162.
SUPPLEMENTARY INFORMATION: When submitting comments or requesting
information, please include the document identifier HHS-OS-19060-60D
for reference.
Information Collection Request Title: Living Healthier, Living
Longer Program Evaluation.
Abstract: The Department of Health and Human Services (HHS), the
Office of Women's Health, (OWH) Coordinating Committee on Lesbian, Gay,
Bi-sexual and Transgender (LGBT) Issues has prioritized the collection
of health data on LGBT populations. In response, OWH funded an
initiative to ``identify and test effective and innovative ways of
reducing obesity in lesbian and bisexual women'' (HHS, 2012). This
initiative will include nutritional and physical activity counseling
and activities, and will be implemented in New York City. It will be
tailored to bisexual and lesbian women forty years and over. Evaluation
of the initiative will address the following questions: (1) Does a
healthy weight intervention based on the individual and the social
environment improve health and reduce weight of older lesbian and
bisexual women; and, (2) If the intervention does improve health and/or
reduce weight, what attributes of the intervention contributed to this
success? Information will be gathered and analyzed in an effort to
identify and understand the effects of this healthy weight intervention
and to inform the applicability of the intervention to other sites
across the United States. The project is scheduled for one year.
Total Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Form name respondents responses per response (in hours
respondent hours)
----------------------------------------------------------------------------------------------------------------
Baseline Survey................................. 40 1 15/60 10
Study Completion Survey......................... 40 1 15/60 10
Pedometer Profile............................... 40 1 2/60 1
Health Screen (physical measurement)............ 40 3 10/60 20
Health History Questionnaire.................... 40 1 12/60 8
Intervention Experience Study Mid-Point)........ 40 1 1 40 hours
Intervention Experience ( Study Completion)..... 40 1 1 40 hours
---------------------------------------------------------------
Total....................................... .............. .............. .............. 129 hours
----------------------------------------------------------------------------------------------------------------
OS specifically requests comments on (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.
Keith A. Tucker,
Information Collection Clearance Officer.
[FR Doc. 2013-05609 Filed 3-11-13; 8:45 am]
BILLING CODE 4150-33-P
