Proposed Data Collection Submitted for Public Comment and Recommendations, 50131-50133 [2017-23561]
Download as PDF
<![CDATA[
sradovich on DSK3GMQ082PROD with NOTICES
Federal Register / Vol. 82, No. 208 / Monday, October 30, 2017 / Notices
Additionally, the FTC complaint
alleges that the respondent, in certain of
its articles, emails, and social media
posts, misrepresented that its
endorsements were independent and
not paid advertising, and failed to
adequately disclose that the content
recommended schools that paid the
respondent specifically to be promoted
therein. The proposed complaint alleges
that those misrepresentations and
undisclosed paid recommendations
constitute deceptive acts or practices
under Section 5 of the FTC Act.
The proposed order is designed to
prevent the respondent from engaging in
similar deceptive practices in the future.
Part I prohibits the respondent from
making any misrepresentations
regarding the scope of any search tool,
including whether the tool only
searches ‘‘military friendly’’ schools.
Part I further prohibits the respondent
from making any misrepresentations
about material connections between it
and any schools, and from making any
misrepresentations that paid
commercial advertising is independent
content.
Part II requires the respondent, when
endorsing schools (or preparing thirdparty endorsements of schools), to
clearly and conspicuously disclose, in
close proximity to the endorsement, any
payments or other material connections
between the respondent or the other
endorser and the school. This disclosure
requirement applies where consumers
are likely to believe that such
endorsements reflect the beliefs of the
respondent or other endorser (and not
the schools themselves).
Parts III through VII of the proposed
order are reporting and compliance
provisions.
Part III is an order distribution
provision. Part IV requires the
respondent to submit a compliance
report one year after the issuance of the
order, and to notify the Commission of
corporate changes that may affect
compliance obligations. Part V requires
the respondent to create, for 10 years,
accounting, personnel, complaint, and
advertising records, and to maintain
each of those records for 5 years. Part VI
requires the respondent to submit
additional compliance reports within 10
business days of a written request by the
Commission, and to permit voluntary
interviews with persons affiliated with
the respondent. Part VII ‘‘sunsets’’ the
order after twenty years, with certain
exceptions.
The purpose of this analysis is to aid
public comment on the proposed order.
It is not intended to constitute an
official interpretation of the complaint
VerDate Sep<11>2014
17:59 Oct 27, 2017
Jkt 244001
or proposed order, or to modify in any
way the proposed order’s terms.
By direction of the Commission.
Donald S. Clark,
Secretary.
[FR Doc. 2017–23514 Filed 10–27–17; 8:45 am]
BILLING CODE 6750–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–18–0932; Docket No. CDC–2018–
0094]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
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 effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies the opportunity to comment on
a proposed and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled Information Collection for
Evaluation of Education,
Communication, and Training Activities
for Mobile Populations. This data
collection will enable to evaluate its
mobile populations and stakeholders
communication, training, and education
material’s effectiveness.
DATES: CDC must receive written
comments on or before December 29,
2017.
SUMMARY:
You may submit comments,
identified by Docket No. CDC–2018–
0094 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.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. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all Federal
comments through the Federal
ADDRESSES:
PO 00000
Frm 00016
Fmt 4703
Sfmt 4703
50131
eRulemaking portal (regulations.gov) or
by U.S. mail to the address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Leroy A.
Richardson, Information Collection
Review Office, Centers for Disease
Control and Prevention, 1600 Clifton
Road NE., MS–D74, Atlanta, Georgia
30329; phone: 404–639–7570; Email:
omb@cdc.gov.
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 the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions 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 through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submissions
of responses.
5. Assess information collection costs.
Proposed Project
Information Collection for Evaluation
of Education, Communication, and
Training Activities for Mobile
Populations (OMB Control Number
0920–0932, Expires 7/31/2018)—
Extension—National Center for
Emerging and Zoonotic Infectious
E:\FR\FM\30OCN1.SGM
30OCN1
50132
Federal Register / Vol. 82, No. 208 / Monday, October 30, 2017 / Notices
Diseases (NCEZID), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
The CDC’s Division of Global
Migration and Quarantine (DGMQ)
seeks to request a three-year extension
of a currently approved generic
information collection plan to conduct
evaluation research. Information
gathered from this plan’s associated data
collections will help CDC plan and
implement health communication,
education, and training activities to
improve health and prevent the spread
of disease. These activities include
communicating, educating, and training
with international travelers and other
mobile populations, training healthcare
providers, and educating public health
departments, federal partners, and other
stakeholders.
CDC proposes to change the current
title of this generic plan from
‘‘Information Collection for Evaluation
of Education, Communication, and
Training Activities for the Division of
Global Migration and Quarantine’’ to
‘‘Information Collection for Evaluation
of Education, Communication, and
Training Activities for Mobile
Populations.’’
In the past three years, OMB approved
two individual information collections
under this generic plan, where both
resulted in collaborations between
multiple divisions within the NCEZID.
information collection plan will help
DGMQ continue to refine efforts prove
valuable for communication activities
that must occur quickly in response to
public health emergencies.
DGMQ staff will use a variety of data
collection methods for this proposed
project: Interviews, focus groups,
surveys, and pre/post-tests. Depending
on the research questions and audiences
involved, data may be gathered inperson, by telephone, online, or using
some combination of these formats. CDC
may collect data in quantitative and/or
qualitative forms. CDC will assess
numerous audience variables under the
auspices of this generic information
collection plan. These include, but are
not limited to, knowledge, attitudes,
beliefs, behavioral intentions, practices,
behaviors, skills, self-efficacy, and
information needs and sources. Insights
gained from evaluation research will
assist in the development, refinement,
implementation, and demonstration of
outcomes and impact of
communication, education, and training
activities.
DGMQ estimates that 17,500
respondents and 7,982 hours of burden
will be involved in evaluation research
activities each year. The collected
information will not impose a cost
burden on the respondents beyond that
associated with their time to provide the
required data.
DGMQ proposes a less exclusive project
title because multiple divisions across
NCEZID frequently collaborate on
various activities. DGMQ does not
propose any other changes for this
extension request.
DGMQ has aligned the proposed
information collections with DGMQ’s
mission to reduce morbidity and
mortality among immigrants, refugees,
travelers, expatriates, and other globally
mobile populations, and to prevent the
introduction, transmission, or spread of
communicable diseases from foreign
countries into the United States. This
mission is supported by delegated legal
authorities outlined in the Public Health
Service (PHS) Act (42 U.S.C. 264) and
in regulations that are codified in 42
Code of Federal Regulations (CFR) parts
70 and 71, and 34.
Approval of this extension request
will enable DGMQ to continue
collecting information in an expedited
manner. To help improve and inform
activities during both routine and
emergency public health events, DGMQ
seeks to collect the following
information types: Knowledge,
attitudes, and behaviors of key
audiences (such as refugees,
immigrants, migrants, international
travelers, travel industry partners,
healthcare providers, non-profit
agencies, customs brokers and
forwarders, schools, state and local
health departments). This generic
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
(in hours)
Form name
General Public ..................................
Healthcare Professionals ..................
General Public ..................................
Healthcare Professionals ..................
General Public ..................................
Healthcare Professionals ..................
General Public ..................................
Healthcare Professionals Interviews
General Public ..................................
Healthcare Professionals ..................
General Public ..................................
Healthcare Professionals ..................
General Public ..................................
Healthcare Professionals ..................
Focus Groups Screening form .........
Focus Groups Screening form .........
Focus Groups ...................................
Focus Groups ...................................
Interview Screening Form ................
Interview Screening Form ................
Interviews .........................................
Interviews .........................................
Survey Screening Forms .................
Survey Screening Forms .................
Surveys ............................................
Surveys ............................................
Pre/Post Tests ..................................
Pre/Post Tests ..................................
1,050
450
525
225
700
300
350
150
5,250
2,250
2,625
1,125
1,750
750
1
1
1
1
1
1
1
1
1
1
1
1
1
1
10/60
10/60
90/60
90/60
10/60
10/60
1
1
10/60
10/60
45/60
45/60
45/60
45/60
175
75
788
338
117
50
350
150
875
375
1,969
844
1,313
563
Total ...........................................
sradovich on DSK3GMQ082PROD with NOTICES
Type of respondents
...........................................................
........................
........................
........................
7,982
VerDate Sep<11>2014
17:59 Oct 27, 2017
Jkt 244001
PO 00000
Frm 00017
Fmt 4703
Sfmt 9990
E:\FR\FM\30OCN1.SGM
30OCN1
50133
Federal Register / Vol. 82, No. 208 / Monday, October 30, 2017 / Notices
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. 2017–23561 Filed 10–27–17; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Proposed Projects
Title: Multistate Financial Institution
Data Match and Federally Assisted State
Transmitted Levy (MSFIDM/FAST
Levy).
OMB No.: 0970–0196.
Description: Section 466(a)(17) of the
Social Security Act (the Act) requires
states to establish procedures for their
child support agencies to enter into
agreements with financial institutions
doing business in their state for the
purpose of securing information leading
to the enforcement of child support
orders. Under 452(m) and
466(a)(17)(A)(i) of the Act, the Secretary
may aid state agencies conducting data
matches with financial institutions
doing business in two or more states by
establishing a centralized and
standardized matching program through
the Federal Parent Locator Service.
To further assist states collect child
support, the federal Office of Child
Support Enforcement (OCSE) worked
with child support agencies and
financial institutions to develop the
Federally Assisted State Transmitted
(FAST) Levy system.
FAST Levy is a central, standardized,
and secure electronic process for child
support agencies and financial
institutions to exchange information
about levying financial accounts to
collect past-due support. OCSE picks up
files created by child support agencies
that contain FAST Levy requests and
distributes them to financial institutions
that use the FAST Levy system. Those
financial institutions create response
files that OCSE picks up and distributes
to the child support agencies.
The MSFIDM/FAST-Levy information
collection activities are authorized by:
42 U.S.C. 652(m), which authorizes
OCSE, through the Federal Parent
Locator Service, to aid state child
support agencies and financial
institutions doing business in two or
more states reach agreements regarding
the receipt from financial institutions,
and the transfer to the state child
support agencies, of information
pertaining to the location of accounts
held by obligors who owe past-due
support; 42 U.S.C. 666(a)(2) and
(c)(1)(G)(ii), which require state child
support agencies in cases in which there
is an arrearage to establish procedures to
secure assets to satisfy any current
support obligation and the arrearage by
attaching and seizing assets of the
obligor held in financial institutions; 42
U.S.C. 666(a)(17)(A), which requires
state child support agencies to establish
procedures under which the state child
support agencies shall enter into
agreements with financial institutions
doing business in the State to develop
and operate, in coordination with
financial institutions, and the Federal
Parent Locator Service (in the case of
financial institutions doing business in
two or more States), a data match
system, using automated data exchanges
to the maximum extent feasible, in
which a financial institution is required
to quarterly provide information
pertaining to a noncustodial parent
owing past-due support who maintains
an account at the institution and, in
response to a notice of lien or levy,
encumber or surrender, assets held; 42
U.S.C. 652(a)(7), which requires OCSE
to provide technical assistance to state
child support enforcement agencies to
help them establish effective systems for
collecting child and spousal support;
and, 45 CFR 303.7(a)(5), which requires
state child support agencies to transmit
requests for information and provide
requested information electronically to
the greatest extent possible. To facilitate
this requirement for states, OCSE
developed the FAST Levy system that
supports the electronic exchange of lien
and levy information between child
support agencies and financial
institutions.
Respondents: Multistate Financial
Institutions and State Child Support
Agencies.
ANNUAL BURDEN ESTIMATES
Number of
responses per
respondent
Number of
respondents
Instrument
Financial Data Match Result File-Portal ..........................................................
Election Form ...................................................................................................
FAST-Levy Record Specifications: Current Financial Institutions Users to
Program New Codes ....................................................................................
FAST-Levy Record Specifications: Current State Child Support Agencies to
Program New Codes ....................................................................................
FAST-Levy Response Withhold Record Specifications: Financial Institutions
FAST-Levy Request Withhold Record Specifications: State Child Support
Agencies .......................................................................................................
Average
burden hours
per response
Total burden
hours
192
30
4
1
5 minutes 1
0.5
64
15
1
1
65 2
65
3
1
1
1
65
1,716
195
1,716
2
1
1,610
3,220
1 Estimate
sradovich on DSK3GMQ082PROD with NOTICES
is approximately 5 minutes per response. For calculation, use 5/60.
2 Estimate is an average based on input from OCSE’s matching partners.
Estimated Total Annual Burden
Hours: 5,275.
Additional Information: Copies of the
proposed collection may be obtained by
writing to the Administration for
Children and Families, Office of
Planning, Research and Evaluation, 330
C Street SW., Washington, DC 20201,
Attention Reports Clearance Officer. All
requests should be identified by the
VerDate Sep<11>2014
17:59 Oct 27, 2017
Jkt 244001
information collection. Email address:
infocollection@acf.hhs.gov
OMB Comment: OMB is required to
make a decision concerning the
collection of information between 30
and 60 days after publication of this
document in the Federal Register.
Therefore, a comment is best assured of
having its full effect if OMB receives it
within 30 days of publication. Written
PO 00000
Frm 00018
Fmt 4703
Sfmt 4703
comments and recommendations for the
proposed information collection should
be sent directly to the following: Office
of Management and Budget, Paperwork
Reduction Project, Email: OIRA_
SUBMISSION@OMB.EOP.GOV, Attn:
E:\FR\FM\30OCN1.SGM
30OCN1
]]>Agencies
[Federal Register Volume 82, Number 208 (Monday, October 30, 2017)]
[Notices]
[Pages 50131-50133]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-23561]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-18-0932; Docket No. CDC-2018-0094]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: The Centers for Disease Control and Prevention (CDC), as part
of its continuing effort to reduce public burden and maximize the
utility of government information, invites the general public and other
Federal agencies the opportunity to comment on a proposed and/or
continuing information collection, as required by the Paperwork
Reduction Act of 1995. This notice invites comment on a proposed
information collection project titled Information Collection for
Evaluation of Education, Communication, and Training Activities for
Mobile Populations. This data collection will enable to evaluate its
mobile populations and stakeholders communication, training, and
education material's effectiveness.
DATES: CDC must receive written comments on or before December 29,
2017.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2018-
0094 by any of the following methods:
Federal eRulemaking Portal: Regulations.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. CDC will post, without change, all relevant comments
to Regulations.gov.
Please note: Submit all Federal comments through the Federal
eRulemaking portal (regulations.gov) or by U.S. mail to the address
listed above.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the information collection plan
and instruments, contact Leroy A. Richardson, 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 the OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
The OMB is particularly interested in comments that will help:
1. Evaluate whether the proposed collection of information is
necessary for the proper performance of the functions 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 through the use of appropriate automated,
electronic, mechanical, or other technological collection techniques or
other forms of information technology, e.g., permitting electronic
submissions of responses.
5. Assess information collection costs.
Proposed Project
Information Collection for Evaluation of Education, Communication,
and Training Activities for Mobile Populations (OMB Control Number
0920-0932, Expires 7/31/2018)--Extension--National Center for Emerging
and Zoonotic Infectious
[[Page 50132]]
Diseases (NCEZID), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
The CDC's Division of Global Migration and Quarantine (DGMQ) seeks
to request a three-year extension of a currently approved generic
information collection plan to conduct evaluation research. Information
gathered from this plan's associated data collections will help CDC
plan and implement health communication, education, and training
activities to improve health and prevent the spread of disease. These
activities include communicating, educating, and training with
international travelers and other mobile populations, training
healthcare providers, and educating public health departments, federal
partners, and other stakeholders.
CDC proposes to change the current title of this generic plan from
``Information Collection for Evaluation of Education, Communication,
and Training Activities for the Division of Global Migration and
Quarantine'' to ``Information Collection for Evaluation of Education,
Communication, and Training Activities for Mobile Populations.''
In the past three years, OMB approved two individual information
collections under this generic plan, where both resulted in
collaborations between multiple divisions within the NCEZID. DGMQ
proposes a less exclusive project title because multiple divisions
across NCEZID frequently collaborate on various activities. DGMQ does
not propose any other changes for this extension request.
DGMQ has aligned the proposed information collections with DGMQ's
mission to reduce morbidity and mortality among immigrants, refugees,
travelers, expatriates, and other globally mobile populations, and to
prevent the introduction, transmission, or spread of communicable
diseases from foreign countries into the United States. This mission is
supported by delegated legal authorities outlined in the Public Health
Service (PHS) Act (42 U.S.C. 264) and in regulations that are codified
in 42 Code of Federal Regulations (CFR) parts 70 and 71, and 34.
Approval of this extension request will enable DGMQ to continue
collecting information in an expedited manner. To help improve and
inform activities during both routine and emergency public health
events, DGMQ seeks to collect the following information types:
Knowledge, attitudes, and behaviors of key audiences (such as refugees,
immigrants, migrants, international travelers, travel industry
partners, healthcare providers, non-profit agencies, customs brokers
and forwarders, schools, state and local health departments). This
generic information collection plan will help DGMQ continue to refine
efforts prove valuable for communication activities that must occur
quickly in response to public health emergencies.
DGMQ staff will use a variety of data collection methods for this
proposed project: Interviews, focus groups, surveys, and pre/post-
tests. Depending on the research questions and audiences involved, data
may be gathered in-person, by telephone, online, or using some
combination of these formats. CDC may collect data in quantitative and/
or qualitative forms. CDC will assess numerous audience variables under
the auspices of this generic information collection plan. These
include, but are not limited to, knowledge, attitudes, beliefs,
behavioral intentions, practices, behaviors, skills, self-efficacy, and
information needs and sources. Insights gained from evaluation research
will assist in the development, refinement, implementation, and
demonstration of outcomes and impact of communication, education, and
training activities.
DGMQ estimates that 17,500 respondents and 7,982 hours of burden
will be involved in evaluation research activities each year. The
collected information will not impose a cost burden on the respondents
beyond that associated with their time to provide the required data.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response Total burden
respondents respondent (in hours) (in hours)
----------------------------------------------------------------------------------------------------------------
General Public................ Focus Groups 1,050 1 10/60 175
Screening form.
Healthcare Professionals...... Focus Groups 450 1 10/60 75
Screening form.
General Public................ Focus Groups.... 525 1 90/60 788
Healthcare Professionals...... Focus Groups.... 225 1 90/60 338
General Public................ Interview 700 1 10/60 117
Screening Form.
Healthcare Professionals...... Interview 300 1 10/60 50
Screening Form.
General Public................ Interviews...... 350 1 1 350
Healthcare Professionals Interviews...... 150 1 1 150
Interviews.
General Public................ Survey Screening 5,250 1 10/60 875
Forms.
Healthcare Professionals...... Survey Screening 2,250 1 10/60 375
Forms.
General Public................ Surveys......... 2,625 1 45/60 1,969
Healthcare Professionals...... Surveys......... 1,125 1 45/60 844
General Public................ Pre/Post Tests.. 1,750 1 45/60 1,313
Healthcare Professionals...... Pre/Post Tests.. 750 1 45/60 563
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 7,982
----------------------------------------------------------------------------------------------------------------
[[Page 50133]]
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. 2017-23561 Filed 10-27-17; 8:45 am]
BILLING CODE 4163-18-P
