Agency Information Collection Activities: Proposed Collection; Comment Request, 46080-46081 [2016-16797]
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46080
Federal Register / Vol. 81, No. 136 / Friday, July 15, 2016 / Notices
appearing below the YouTube videos.
Warner Bros. did not require the
YouTube influencers to place a
sponsorship disclosure clearly and
conspicuously in the video itself. Nor
did Warner Bros. require that the
YouTube influencers be instructed to
place the sponsorship disclosure ‘‘above
the fold’’ in the description box, or
visible without consumers having to
scroll down or click on a link, as it had
for other promotional information about
Shadow of Mordor. (See, e.g., Exhibit A–
1) As a result, most YouTube
influencers did not include any
sponsorship disclosures in their videos,
and only placed their sponsorship
disclosures ‘‘below the fold’’ in the
description box below the video.
Therefore, consumers had to click on a
‘‘Show More’’ button in the description
box and potentially scroll down before
they could see the sponsorship
disclosure. As a result, consumers who
watched these YouTube videos were
unlikely to learn that the videos were
paid promotions for Warner Bros.
The Commission’s complaint further
alleges that when YouTube influencers
posted their Shadow of Mordor videos
for viewing on Facebook or Twitter,
consumers were even less likely to see
these sponsorship disclosures because
such posts did not include the ‘‘Show
More’’ button. In addition, the
complaint states that on at least two
occasions, the influencers disclosed
only that they had been given early
access to the game, and did not
adequately disclose that they had also
been paid to post the video.
According to the complaint, in
numerous instances, YouTube
influencers did not disclose or
adequately disclose that Warner Bros.,
through Plaid Social, offered
compensation to the influencers in
exchange for creating and uploading
gameplay videos as part of a Shadow of
Mordor advertising campaign. The
Commission’s complaint alleges that
these videos were false and misleading
because they did not reflect the
independent opinions or experiences of
impartial video game enthusiasts. The
complaint further alleges that the videos
were deceptive because they failed to
disclose or disclose adequately that the
influencers who posted the videos were
compensated in connection with their
endorsements.
The proposed order includes
injunctive relief to address these alleged
violations and requires Warner Bros. to
follow certain monitoring and
compliance procedures related to its use
of influencer campaigns.
Part I of the proposed order prohibits
Warner Bros., in connection with the
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advertising of any home entertainment
product or service, from
misrepresenting in any influencer
campaign that an influencer or endorser
of such product or service is an
independent user or ordinary consumer
of the product or service.
Part II of the proposed order requires
Warner Bros., in connection with the
advertising of any home entertainment
product or service by means of an
endorsement, in any influencer
campaign, to disclose clearly and
conspicuously a material connection, if
one exists, between the influencer or
endorser and Warner Bros.
Part III of the proposed order sets out
certain monitoring and compliance
obligations to ensure that Warner Bros.,
or any entity it engages to conduct an
influencer campaign, comply with Parts
I and II of the proposed order. These
obligations include: Obtaining signed
acknowledgements from such
influencers that they will disclose their
material connection to Warner Bros.;
monitoring the influencers’
representations and disclosures;
maintaining records of monitoring
efforts; and, under certain
circumstances, terminating and ceasing
payment to influencers who
misrepresent their independence, or fail
to properly disclose any material
connection to Warner Bros. Part III
specifically provides that if Warner
Bros. engages an entity to conduct an
influencer campaign, Warner Bros. must
take steps to ensure that the entity
complies with this Part, and to monitor
its compliance. If the entity fails to
comply with this Part, Warner Bros.
must cease payment to the entity until
it cures any noncompliance.
Furthermore, Warner Bros. is required
to disqualify the entity from conducting
future influencer campaigns upon a
repeat incident, unless it reasonably
concludes that the entity’s failure to
comply was inadvertent.
Part IV of the proposed order contains
recordkeeping requirements for relevant
documents.
Parts V through VII of the proposed
order require the company to: Provide
copies of the order to certain personnel
having responsibilities with respect to
the subject matter of the order; notify
the Commission of changes in corporate
structure that might affect compliance
obligations under the order; and file
compliance reports with the
Commission.
Part VIII of the proposed order
provides that the order will terminate
after twenty (20) years, with certain
exceptions.
The purpose of this analysis is to
facilitate public comment on the
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proposed order, and it is not intended
to constitute an official interpretation of
the complaint or proposed order, or to
modify the proposed order’s terms in
any way.
By direction of the Commission.
Donald S. Clark,
Secretary.
[FR Doc. 2016–16729 Filed 7–14–16; 8:45 am]
BILLING CODE 6750–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–339 and CMS–
460]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, HHS.
ACTION: Notice.
AGENCY:
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995 (the
PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information (including each proposed
extension or reinstatement of an existing
collection of information) and to allow
60 days for public comment on the
proposed action. Interested persons are
invited to send comments regarding our
burden estimates 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
automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
DATES: Comments must be received by
September 13, 2016.
ADDRESSES: When commenting, please
reference the document identifier or
OMB control number. To be assured
consideration, comments and
recommendations must be submitted in
any one of the following ways:
1. Electronically. You may send your
comments electronically to https://
www.regulations.gov. Follow the
SUMMARY:
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15JYN1
Federal Register / Vol. 81, No. 136 / Friday, July 15, 2016 / Notices
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) that are accepting
comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number llll, Room C4–26–
05, 7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, you may make your request
using one of the following:
1. Access CMS’ Web site address at
https://www.cms.hhs.gov/
PaperworkReductionActof1995.
2. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at
(410) 786–1326.
FOR FURTHER INFORMATION CONTACT:
Reports Clearance Office at (410) 786–
1326.
SUPPLEMENTARY INFORMATION:
Contents
This notice sets out a summary of the
use and burden associated with the
following information collections. More
detailed information can be found in
each collection’s supporting statement
and associated materials (see
ADDRESSES).
CMS–339 Provider Cost Report
Reimbursement Questionnaire
sradovich on DSK3GMQ082PROD with NOTICES
CMS–460 Medicare Participation
Agreement for Physicians and
Suppliers
Under the 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.
The term ‘‘collection of information’’ is
defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA
requires federal agencies to publish a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, before
submitting the collection to OMB for
approval. To comply with this
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19:03 Jul 14, 2016
Jkt 238001
requirement, CMS is publishing this
notice.
Information Collection
1. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Provider Cost
Report Reimbursement Questionnaire;
Use: The information collected in this
form (Exhibits 1 and 2) is authorized
under Sections 1815(a) and 1833(e) of
the Social Security Act, 42 U.S.C. 1395g.
Regulations at 42 CFR 413.20 and
413.24 require providers to submit
financial and statistical records to verify
the cost data disclosed on their annual
Medicare cost report. Providers
participating in the Medicare program
are reimbursed for furnishing covered
services to eligible beneficiaries on the
basis of an annual cost report (filed with
the provider’s MAC) in which the
proper reimbursement is computed.
Consequently, it is necessary to collect
this documentation of providers’ costs
and activities that supports the
Medicare cost report data in order to
ensure proper Medicare reimbursement
to providers. Form Number: CMS–339
(OMB control number: 0938–0301);
Frequency: Yearly; Affected Public:
Private sector (Business or other Forprofits); Number of Respondents: 2,273;
Total Annual Responses: 2,273; Total
Annual Hours: 15,911. (For policy
questions regarding this collection
contact Christine Dobrzycki at 410–786–
3389.)
2. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Medicare
Participation Agreement for Physicians
and Suppliers; Use: Section 1842(h) of
the Social Security Act permits
physicians and suppliers to voluntarily
participate in Medicare Part B by
agreeing to take assignment on all
claims for services to Medicare
beneficiaries. The law also requires that
the Secretary provide specific benefits
to the physicians, suppliers and other
persons who choose to participate. The
CMS–460 is the agreement by which the
physician or supplier elects to
participate in Medicare. Form Number:
CMS–460 (OMB control number: 0938–
0373); Frequency: Yearly; Affected
Public: Private sector (Business or other
For-profits); Number of Respondents:
120,000; Total Annual Responses:
120,000; Total Annual Hours: 30,000.
(For policy questions regarding this
collection contact Mark Baldwin at 410–
786–8139.)
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46081
Dated: July 12, 2016.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2016–16797 Filed 7–14–16; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–3333–N2]
Medicare Program; Announcement of
Requirements and Registration for the
MIPS Mobile Challenge; Deadline
Extension
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Notice.
AGENCY:
This notice launches a
challenge related to the new Merit-based
Incentive Payment System (MIPS)
program, which will assist the Centers
for Medicare & Medicaid Services (CMS)
in accelerating the transition from the
traditional fee-for-service payment
model to a system that rewards health
care providers for providing better care,
not just more care. This challenge will
address one of the most important
aspects of our programs, which is
educating and providing outreach to the
potential hundreds of thousands of
MIPS eligible clinicians.
DATES: Important dates concerning the
Challenge include the following:
MIPS Mobile Challenge: To be
announced on www.challenge.gov and
opened for submissions in
www.challenge.gov April 25, 2016.
Deadline for Phase I Submissions:
August 15, 2016.
HHS announces top three-five
challenge applicants and launches
Phase II. Applicants that did not win
Phase I will be permitted to compete for
Phase II: August 30, 2016.
Deadline for Phase II Submissions:
October 31, 2016.
HHS announces grand prize winner:
November 15, 2016 (tentative).
FOR FURTHER INFORMATION CONTACT: Stan
Ostrow, (410) 786–7207 for inquiry on
Information Systems Group.
SUPPLEMENTARY INFORMATION:
SUMMARY:
I. Background
The Medicare Access and CHIP
Reauthorization Act of 2015 (Pub. L.
114–10, enacted April 16, 2015)
(MACRA) requires the Secretary to
establish a new Merit-based Incentive
Payment System (MIPS) program, which
E:\FR\FM\15JYN1.SGM
15JYN1
Agencies
[Federal Register Volume 81, Number 136 (Friday, July 15, 2016)]
[Notices]
[Pages 46080-46081]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-16797]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifiers: CMS-339 and CMS-460]
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Centers for Medicare & Medicaid Services, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Centers for Medicare & Medicaid Services (CMS) is
announcing an opportunity for the public to comment on CMS' intention
to collect information from the public. Under the Paperwork Reduction
Act of 1995 (the PRA), federal agencies are required to publish notice
in the Federal Register concerning each proposed collection of
information (including each proposed extension or reinstatement of an
existing collection of information) and to allow 60 days for public
comment on the proposed action. Interested persons are invited to send
comments regarding our burden estimates 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
automated collection techniques or other forms of information
technology to minimize the information collection burden.
DATES: Comments must be received by September 13, 2016.
ADDRESSES: When commenting, please reference the document identifier or
OMB control number. To be assured consideration, comments and
recommendations must be submitted in any one of the following ways:
1. Electronically. You may send your comments electronically to
https://www.regulations.gov. Follow the
[[Page 46081]]
instructions for ``Comment or Submission'' or ``More Search Options''
to find the information collection document(s) that are accepting
comments.
2. By regular mail. You may mail written comments to the following
address: CMS, Office of Strategic Operations and Regulatory Affairs,
Division of Regulations Development, Attention: Document Identifier/OMB
Control Number ____, Room C4-26-05, 7500 Security Boulevard, Baltimore,
Maryland 21244-1850.
To obtain copies of a supporting statement and any related forms
for the proposed collection(s) summarized in this notice, you may make
your request using one of the following:
1. Access CMS' Web site address at https://www.cms.hhs.gov/PaperworkReductionActof1995.
2. Email your request, including your address, phone number, OMB
number, and CMS document identifier, to Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at (410) 786-1326.
FOR FURTHER INFORMATION CONTACT: Reports Clearance Office at (410) 786-
1326.
SUPPLEMENTARY INFORMATION:
Contents
This notice sets out a summary of the use and burden associated
with the following information collections. More detailed information
can be found in each collection's supporting statement and associated
materials (see ADDRESSES).
CMS-339 Provider Cost Report Reimbursement Questionnaire
CMS-460 Medicare Participation Agreement for Physicians and Suppliers
Under the 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. The term
``collection of information'' is defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests or requirements that members of
the public submit reports, keep records, or provide information to a
third party. Section 3506(c)(2)(A) of the PRA requires federal agencies
to publish a 60-day notice in the Federal Register concerning each
proposed collection of information, including each proposed extension
or reinstatement of an existing collection of information, before
submitting the collection to OMB for approval. To comply with this
requirement, CMS is publishing this notice.
Information Collection
1. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Provider Cost
Report Reimbursement Questionnaire; Use: The information collected in
this form (Exhibits 1 and 2) is authorized under Sections 1815(a) and
1833(e) of the Social Security Act, 42 U.S.C. 1395g. Regulations at 42
CFR 413.20 and 413.24 require providers to submit financial and
statistical records to verify the cost data disclosed on their annual
Medicare cost report. Providers participating in the Medicare program
are reimbursed for furnishing covered services to eligible
beneficiaries on the basis of an annual cost report (filed with the
provider's MAC) in which the proper reimbursement is computed.
Consequently, it is necessary to collect this documentation of
providers' costs and activities that supports the Medicare cost report
data in order to ensure proper Medicare reimbursement to providers.
Form Number: CMS-339 (OMB control number: 0938-0301); Frequency:
Yearly; Affected Public: Private sector (Business or other For-
profits); Number of Respondents: 2,273; Total Annual Responses: 2,273;
Total Annual Hours: 15,911. (For policy questions regarding this
collection contact Christine Dobrzycki at 410-786-3389.)
2. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Medicare
Participation Agreement for Physicians and Suppliers; Use: Section
1842(h) of the Social Security Act permits physicians and suppliers to
voluntarily participate in Medicare Part B by agreeing to take
assignment on all claims for services to Medicare beneficiaries. The
law also requires that the Secretary provide specific benefits to the
physicians, suppliers and other persons who choose to participate. The
CMS-460 is the agreement by which the physician or supplier elects to
participate in Medicare. Form Number: CMS-460 (OMB control number:
0938-0373); Frequency: Yearly; Affected Public: Private sector
(Business or other For-profits); Number of Respondents: 120,000; Total
Annual Responses: 120,000; Total Annual Hours: 30,000. (For policy
questions regarding this collection contact Mark Baldwin at 410-786-
8139.)
Dated: July 12, 2016.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2016-16797 Filed 7-14-16; 8:45 am]
BILLING CODE 4120-01-P