Information Collection Being Reviewed by the Federal Communications Commission, 30538-30540 [2016-11583]
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jstallworth on DSK7TPTVN1PROD with NOTICES
30538
Federal Register / Vol. 81, No. 95 / Tuesday, May 17, 2016 / Notices
On July 20, 2015, the Commission
released the part 1 R&O in which it
updated many of its part 1 competitive
bidding rules (See Updating Part 1
Competitive Bidding Rules; Expanding
the Economic and Innovation
Opportunities of Spectrum Through
Incentive Auctions; Petition of
DIRECTV Group, Inc. and EchoStar LLC
for Expedited Rulemaking to Amend
Section 1.2105(a)(2)(xi) and 1.2106(a) of
the Commission’s Rules and/or for
Interim Conditional Waiver;
Implementation of the Commercial
Spectrum Enhancement Act and
Modernization of the Commission’s
Competitive Bidding Rules and
Procedures, Report and Order, Order on
Reconsideration of the First Report and
Order, Third Order on Reconsideration
of the Second Report and Order, and
Third Report and Order, FCC 15–80, 30
FCC Rcd 7493 (2015), modified by
Erratum, 30 FCC Rcd 8518 (2015) (Part
1 R&O)). Of relevance to the information
collection at issue here, the
Commission: (1) Implemented a new
general prohibition on the filing of
auction applications by entities
controlled by the same individual or set
of individuals (but with a limited
exception for qualifying rural wireless
partnerships); (2) modified the
eligibility requirements for small
business benefits, and updated the
standardized schedule of small business
sizes, including the gross revenues
thresholds used to determine eligibility;
(3) established a new bidding credit for
eligible rural service providers; (4)
adopted targeted attribution rules to
prevent the unjust enrichment of
ineligible entities; and (5) adopted rules
prohibiting joint bidding arrangements
with limited exceptions. The updated
Part 1 rules apply to applicants seeking
licenses and permits.
Additionally, on June 2, 2014 the
Commission released the Mobile
Spectrum Holdings R&O, in which the
Commission updated its spectrum
screen and established rules for its
upcoming auctions of low-band
spectrum. Of relevance to the
information collection at issue here, the
Commission stated that it could reserve
spectrum in order to ensure against
excessive concentration in holdings of
below-1–GHz spectrum (In the Matter of
Policies Regarding Mobile Spectrum
Holdings, Expanding the Economic and
Innovation Opportunities of Spectrum
Through Incentive Auctions, FCC 14–
63, Report and Order, 29 FCC Rcd 6133,
90) 135 (2014) (Mobile Spectrum
Holdings R&O). See also Application
Procedures for Broadcast Incentive
Auction Scheduled to Begin on March
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15:32 May 16, 2016
Jkt 238001
29, 2016; Technical Formulas for
Competitive Bidding, Public Notice, 30
FCC Rcd 11034, Appendix 3 (WTB
2015); Wireless Telecommunications
Bureau Releases Updated List of
Reserve-Eligible Nationwide Service
Providers in each PEA for the Broadcast
Incentive Auction, Public Notice, AU
No. 14–252 (WTB 2016).
The Commission seeks approval for
revisions to its previously approved
collection of information under OMB
Control Number 3060–0798 to permit
the collection of the additional
information for Commission licenses
and permits, pursuant to the rules and
information collection requirements
adopted by the Commission in the Part
1 R&O and the Mobile Spectrum
Holdings R&O. As part of the collection,
the Commission is seeking approval for
the information collection and
recordkeeping requirements associated
with 47 CFR 1.2210(j), 1.2112(b)(2)(iii),
1.2112(b)(2)(v), 1.2112(b)(2)(vii), and
1.2112(b)(2)(viii). Also, in certain
circumstances, the Commission requires
the applicant to provide copies of their
agreements and/or submit exhibits.
In addition, the Commission seeks
approval for various other, nonsubstantive editorial/consistency edits
and updates to FCC Form 601 that
correct inconsistent capitalization of
words and other typographical errors,
and better align the text on the form
with the text in the Commission rules
both generally and in connection with
recent non-substantive, organizational
amendments to the Commission’s rules.
The Commission therefore seeks
approval for a revision to its currently
approved information collection on FCC
Form 601 to revise FCC Form 601
accordingly.
Federal Communications Commission.
Marlene H. Dortch,
Secretary, Office of the Secretary.
[FR Doc. 2016–11582 Filed 5–16–16; 8:45 am]
BILLING CODE 6712–01–P
FEDERAL COMMUNICATIONS
COMMISSION
[OMB 3060–0207]
Information Collection Being Reviewed
by the Federal Communications
Commission
Federal Communications
Commission.
ACTION: Notice and request for
comments.
AGENCY:
As part of its continuing effort
to reduce paperwork burdens, and as
required by the Paperwork Reduction
SUMMARY:
PO 00000
Frm 00024
Fmt 4703
Sfmt 4703
Act (PRA) of 1995 (44 U.S.C. 3501–
3520), the Federal Communications
Commission (FCC or the Commission)
invites the general public and other
Federal agencies to take this
opportunity to comment on the
following information collection.
Comments are requested concerning:
Whether the proposed collection of
information is necessary for the proper
performance of the functions of the
Commission, including whether the
information shall have practical utility;
the accuracy of the Commission’s
burden estimate; ways to enhance the
quality, utility, and clarity of the
information collected; ways to minimize
the burden of the collection of
information on the respondents,
including the use of automated
collection techniques or other forms of
information technology; and ways to
further reduce the information
collection burden on small business
concerns with fewer than 25 employees.
The FCC may not conduct or sponsor
a collection of information unless it
displays a currently valid control
number. No person shall be subject to
any penalty for failing to comply with
a collection of information subject to the
PRA that does not display a valid Office
of Management and Budget (OMB)
control number.
DATES: Written PRA comments should
be submitted on or before July 18, 2016.
If you anticipate that you will be
submitting comments, but find it
difficult to do so within the period of
time allowed by this notice, you should
advise the contact listed below as soon
as possible.
ADDRESSES: Direct all PRA comments to
Nicole Ongele, FCC, via email PRA@
fcc.gov and to Nicole.Ongele@fcc.gov.
FOR FURTHER INFORMATION CONTACT: For
additional information about the
information collection, contact Nicole
Ongele at (202) 418–2991.
SUPPLEMENTARY INFORMATION:
OMB Control Number: 3060–0207.
Title: Part 11—Emergency Alert
System (EAS), Order, FCC 16–32.
Form Number: N/A.
Type of Review: Revision of a
currently approved collection.
Respondents: Business or other forprofit entities, not-for-profit institutions,
and state, local or tribal government.
Number of Respondents and
Responses: 63,080 respondents;
3,596,546 responses.
Estimated Time per Response: 1 hour
(EAS Participants); 20 hours (SECCs).
Frequency of Response: One-time
reporting requirement and
recordkeeping requirement.
Obligation to Respond: Obligatory for
all entities required to participate in
E:\FR\FM\17MYN1.SGM
17MYN1
jstallworth on DSK7TPTVN1PROD with NOTICES
Federal Register / Vol. 81, No. 95 / Tuesday, May 17, 2016 / Notices
EAS. Statutory authority for this
collection of information is contained in
47 U.S.C. 154(i) and 606 of the
Communications Act of 1934, as
amended.
Total Annual Burden: 110,476 hours.
Total Annual Cost: No cost.
Privacy Impact Assessment: No
Impact(s).
Nature and Extent of Confidentiality:
There is no need for confidentiality.
Needs and Uses: Part 11 contains
rules and regulations addressing the
nation’s Emergency Alert System (EAS).
The EAS provides the President with
the capability to provide immediate
communications and information to the
general public at the national, state and
local area level during periods of
national emergency. The EAS also
provides state and local governments
and the National Weather Service with
the capability to provide immediate
communications and information to the
general public concerning emergency
situations posing a threat to life and
property. State and local use of the EAS
is required to be described in State EAS
Plans that are administered by State
Emergency Communications
Committees (SECC) and submitted to
the FCC for approval.
In the Third Report and Order in EB
Docket No. 04–296, FCC 11–12, the
Commission adopted rules establishing
a regulatory structure for a national test
of the EAS. In order for the Commission
to determine the extent to which the
test, and by extension the EAS, was
successful, the FCC adopted rules
requiring EAS Participants, within forty
five (45) days of the date of the first
national EAS test, to record and submit
to the Commission the following testrelated diagnostic information for each
alert received from each message source
monitored at the time of the national
test:
• Whether they received the alert
message during the designated test;
• whether they retransmitted the
alert;
• if they were not able to receive and/
or transmit the alert, their ‘best effort’
diagnostic analysis regarding the
cause(s) for such failure;
• a description of their station
identification and level of designation
(PEP, LP–1, etc.);
• the date/time of receipt of the EAN
message by all stations; the date/time of
PEP station acknowledgement of receipt
of the EAN message to FOC;
• the date/time of initiation of actual
broadcast of the Presidential message;
• the date/time of receipt of the EAT
message by all stations;
• who they were monitoring at the
time of the test, and the make and
VerDate Sep<11>2014
15:32 May 16, 2016
Jkt 238001
• model number of the EAS
equipment that they utilized.
The Third Report and Order indicates
that the national tests of EAS, and
related information collections will
likely be carried out on an annual basis.
On March 10, 2010, OMB approved the
collection as indicated by the related
Notice of Office of Management and
Budget Action notification.
The FCC is submitting this
information collection to the Office of
Management and Budget (OMB) as a
revision of the previously approved
information collection that established
the mandatory Electronic Test Reporting
System (ETRS) that EAS Participants
must utilize to file identifying and test
result data as part of their participation
in nationwide EAS testing. Specifically,
the Order adopted in EB Docket No. 04–
296, FCC 16–32, amends the State EAS
Plan filing requirements set forth at
Section 11.21 of the Commission’s rules
to require EAS Participants (i.e., the
broadcasters, cable systems, and other
service providers subject to the FCC’s
EAS rules) to provide the following
information to their respective SECC,
who in turn will include such
information in the State EAS Plan
submitted to the Commission for
approval:
• A description of any actions taken
by the EAS Participant (acting
individually, in conjunction with other
EAS Participants in the geographic area,
and/or in consultation with state and
local emergency authorities), to make
EAS alert content available in languages
other than English to its non-English
speaking audience(s);
• A description of any future actions
planned by the EAS Participant, in
consultation with state and local
emergency authorities, to provide EAS
alert content in languages other than
English to its non-English speaking
audience(s), along with an explanation
for the EAS Participant’s decision to
plan or not plan such actions; and
• Any other relevant information that
the EAS Participant may wish to
provide.
In addition, in the event that there is
a material change to any of the
information that EAS Participants are
required to furnish their respective
SECCs, EAS Participants must, within
60 days of the occurrence of such
material change, submit aa letter to their
respective SECCs, copying the
Commission’s Public Safety and
Homeland Security Bureau (Bureau)
that describe such change. The SECCs
are required to incorporate the
information in such letters as
amendments to the State EAS Plans on
file with the Bureau.
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Sfmt 4703
30539
This information will be used by FCC
staff to gauge the effectiveness of the
EAS’s capacity to disseminate inlanguage EAS emergency alert content
to persons who communicate in a
language other than English or may have
a limited understanding of the English
language; to determine whether private
and local efforts to disseminate EAS
multilingual content might be
incorporated into the overall national
EAS structure; and to confirm that
private and local EAS multilingual
operations are consistent with national
plans, FCC regulations, and EAS
operation.
The Commission expects that the
costs to EAS Participants to comply
with these reporting requirements will
be minimal, and largely limited to
internal administrative charges
associated with drafting a brief
statement, and submitting that
statement, and any other relevant
information that the EAS Participant
may wish to provide to their SECC for
inclusion into the State EAS Plan for the
state in which the EAS Participant
operates. The Commission further
expects that the vast majority of EAS
Participants are not engaged in
multilingual EAS activities and
therefore will need to submit nothing
more than a very brief statement to their
SECC explaining their decision to plan
or not plan future actions to provide
EAS alert content in languages other
than English to their non-English
speaking audience(s). For the
presumably small percentage of EAS
Participants that actually are engaged in
multilingual EAS activities, the filing
will merely require that they supply a
summary of actions they already have
taken in this regard. Accordingly, the
FCC estimates that complying with the
reporting requirement will take EAS
Participants, on average, approximately
one hour. The FCC estimates that
compiling the EAS Participant
summaries of multilingual EAS
activities and incorporating such
information into the State EAS Plan will
take SECCs, on average, approximately
20 hours.
The following information collection
contained in part 11 may be impacted
by these rule amendments: Section
11.21 requires that state and local EAS
plans be reviewed and approved by the
Chief, Public Safety and Homeland
Security, prior to implementation to
ensure that they are consistent with
national plans, FCC regulations, and
EAS operation.
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30540
Federal Register / Vol. 81, No. 95 / Tuesday, May 17, 2016 / Notices
• If you want to submit a comment
with confidential information that you
do not wish to be made available to the
public, submit the comment as a
written/paper submission and in the
manner detailed (see ‘‘Written/Paper
Submissions’’ and ‘‘Instructions’’).
Federal Communications Commission.
Marlene H. Dortch,
Secretary.
[FR Doc. 2016–11583 Filed 5–16–16; 8:45 am]
BILLING CODE 6712–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2016–D–1224]
Use of Electronic Health Record Data
in Clinical Investigations; Draft
Guidance for Industry; Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice of availability.
The Food and Drug
Administration (FDA or Agency) is
announcing the availability of a draft
guidance for industry entitled ‘‘Use of
Electronic Health Record Data in
Clinical Investigations.’’ The draft
guidance is intended to assist sponsors,
clinical investigators, contract research
organizations, institutional review
boards (IRBs), and other interested
parties on the use of electronic health
record (EHR) data in FDA-regulated
clinical investigations.
DATES: Although you can comment on
any guidance at any time (see 21 CFR
10.115(g)(5)), to ensure that the Agency
considers your comment on this draft
guidance before it begins work on the
final version of the guidance, submit
either electronic or written comments
on the draft guidance by July 18, 2016.
ADDRESSES: You may submit comments
as follows:
jstallworth on DSK7TPTVN1PROD with NOTICES
SUMMARY:
Electronic Submissions
Submit electronic comments in the
following way:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
Comments submitted electronically,
including attachments, to https://
www.regulations.gov will be posted to
the docket unchanged. Because your
comment will be made public, you are
solely responsible for ensuring that your
comment does not include any
confidential information that you or a
third party may not wish to be posted,
such as medical information, your or
anyone else’s Social Security number, or
confidential business information, such
as a manufacturing process. Please note
that if you include your name, contact
information, or other information that
identifies you in the body of your
comments, that information will be
posted on https://www.regulations.gov.
VerDate Sep<11>2014
15:32 May 16, 2016
Jkt 238001
Written/Paper Submissions
Submit written/paper submissions as
follows:
• Mail/Hand deliveryCourier (for
written/paper submissions): Division of
Dockets Management (HFA–305), Food
and Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Division of Dockets
Management, FDA will post your
comment, as well as any attachments,
except for information submitted,
marked and identified, as confidential,
if submitted as detailed in
‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2016–D–1224 for ‘‘Use of Electronic
Health Record Data in Clinical
Investigations; Draft Guidance for
Industry; Availability.’’ Received
comments will be placed in the docket
and, except for those submitted as
‘‘Confidential Submissions,’’ publicly
viewable at https://www.regulations.gov
or at the Division of Dockets
Management between 9 a.m. and 4 p.m.,
Monday through Friday.
• Confidential Submissions—To
submit a comment with confidential
information that you do not wish to be
made publicly available, submit your
comments only as a written/paper
submission. You should submit two
copies total. One copy will include the
information you claim to be confidential
with a heading or cover note that states
‘‘THIS DOCUMENT CONTAINS
CONFIDENTIAL INFORMATION.’’ The
Agency will review this copy, including
the claimed confidential information, in
its consideration of comments. The
second copy, which will have the
claimed confidential information
redacted/blacked out, will be available
for public viewing and posted on https://
www.regulations.gov. Submit both
copies to the Division of Dockets
Management. If you do not wish your
name and contact information to be
made publicly available, you can
provide this information on the cover
sheet and not in the body of your
comments and you must identify this
information as ‘‘confidential.’’ Any
information marked as ‘‘confidential’’
will not be disclosed except in
accordance with 21 CFR 10.20 and other
applicable disclosure law. For more
information about FDA’s posting of
PO 00000
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Fmt 4703
Sfmt 4703
comments to public dockets, see 80 FR
56469, September 18, 2015, or access
the information at: https://www.fda.gov/
regulatoryinformation/dockets/
default.htm.
Docket: For access to the docket to
read background documents or the
electronic and written/paper comments
received, go to https://
www.regulations.gov and insert the
docket number, found in brackets in the
heading of this document, into the
‘‘Search’’ box and follow the prompts
and/or go to the Division of Dockets
Management, 5630 Fishers Lane, Rm.
1061, Rockville, MD 20852.
Submit written requests for single
copies of the draft guidance to the
Division of Drug Information, Center for
Drug Evaluation and Research, Food
and Drug Administration, 10001 New
Hampshire Ave., Hillandale Building,
4th Floor, Silver Spring, MD 20993–
0002; the Office of Communication,
Outreach, and Development, Center for
Biologics Evaluation and Research,
Food and Drug Administration, 10903
New Hampshire Ave., Bldg. 71, Rm.
3128, Silver Spring, MD 20993–0002; or
the Office of the Center Director,
Guidance and Policy Development,
Center for Devices and Radiological
Health, Food and Drug Administration,
10903 New Hampshire Ave., Bldg. 66,
Rm. 5431, Silver Spring, MD 20993–
0002. Send one self-addressed adhesive
label to assist that office in processing
your requests. See the SUPPLEMENTARY
INFORMATION section for electronic
access to the draft guidance document.
FOR FURTHER INFORMATION CONTACT:
Cheryl Grandinetti, Center for Drug
Evaluation and Research, Food and
Drug Administration, 10903 New
Hampshire Ave., Bldg. 51, Rm. 3348,
Silver Spring, MD 20993–0002, 301–
796–2500; Stephen Ripley, Center for
Biologics Evaluation and Research,
Food and Drug Administration, 10903
New Hampshire Ave., Bldg. 71, Rm.
7301, Silver Spring, MD 20993–0002,
240–402–7911; or Irfan Khan, Center for
Devices and Radiological Health, Food
and Drug Administration, 10903 New
Hampshire Ave., Bldg. 66, Rm. 3563,
Silver Spring, MD 20993–0002, 301–
796–7100.
SUPPLEMENTARY INFORMATION:
I. Background
FDA is announcing the availability of
a draft guidance for industry entitled
‘‘Use of Electronic Health Record Data
in Clinical Investigations.’’ The draft
guidance is intended to assist sponsors,
clinical investigators, contract research
organizations, IRBs, and other interested
parties on the use of EHR data in FDA-
E:\FR\FM\17MYN1.SGM
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Agencies
[Federal Register Volume 81, Number 95 (Tuesday, May 17, 2016)]
[Notices]
[Pages 30538-30540]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-11583]
-----------------------------------------------------------------------
FEDERAL COMMUNICATIONS COMMISSION
[OMB 3060-0207]
Information Collection Being Reviewed by the Federal
Communications Commission
AGENCY: Federal Communications Commission.
ACTION: Notice and request for comments.
-----------------------------------------------------------------------
SUMMARY: As part of its continuing effort to reduce paperwork burdens,
and as required by the Paperwork Reduction Act (PRA) of 1995 (44 U.S.C.
3501-3520), the Federal Communications Commission (FCC or the
Commission) invites the general public and other Federal agencies to
take this opportunity to comment on the following information
collection. Comments are requested concerning: Whether the proposed
collection of information is necessary for the proper performance of
the functions of the Commission, including whether the information
shall have practical utility; the accuracy of the Commission's burden
estimate; ways to enhance the quality, utility, and clarity of the
information collected; ways to minimize the burden of the collection of
information on the respondents, including the use of automated
collection techniques or other forms of information technology; and
ways to further reduce the information collection burden on small
business concerns with fewer than 25 employees.
The FCC may not conduct or sponsor a collection of information
unless it displays a currently valid control number. No person shall be
subject to any penalty for failing to comply with a collection of
information subject to the PRA that does not display a valid Office of
Management and Budget (OMB) control number.
DATES: Written PRA comments should be submitted on or before July 18,
2016. If you anticipate that you will be submitting comments, but find
it difficult to do so within the period of time allowed by this notice,
you should advise the contact listed below as soon as possible.
ADDRESSES: Direct all PRA comments to Nicole Ongele, FCC, via email
PRA@fcc.gov and to Nicole.Ongele@fcc.gov.
FOR FURTHER INFORMATION CONTACT: For additional information about the
information collection, contact Nicole Ongele at (202) 418-2991.
SUPPLEMENTARY INFORMATION:
OMB Control Number: 3060-0207.
Title: Part 11--Emergency Alert System (EAS), Order, FCC 16-32.
Form Number: N/A.
Type of Review: Revision of a currently approved collection.
Respondents: Business or other for-profit entities, not-for-profit
institutions, and state, local or tribal government.
Number of Respondents and Responses: 63,080 respondents; 3,596,546
responses.
Estimated Time per Response: 1 hour (EAS Participants); 20 hours
(SECCs).
Frequency of Response: One-time reporting requirement and
recordkeeping requirement.
Obligation to Respond: Obligatory for all entities required to
participate in
[[Page 30539]]
EAS. Statutory authority for this collection of information is
contained in 47 U.S.C. 154(i) and 606 of the Communications Act of
1934, as amended.
Total Annual Burden: 110,476 hours.
Total Annual Cost: No cost.
Privacy Impact Assessment: No Impact(s).
Nature and Extent of Confidentiality: There is no need for
confidentiality.
Needs and Uses: Part 11 contains rules and regulations addressing
the nation's Emergency Alert System (EAS). The EAS provides the
President with the capability to provide immediate communications and
information to the general public at the national, state and local area
level during periods of national emergency. The EAS also provides state
and local governments and the National Weather Service with the
capability to provide immediate communications and information to the
general public concerning emergency situations posing a threat to life
and property. State and local use of the EAS is required to be
described in State EAS Plans that are administered by State Emergency
Communications Committees (SECC) and submitted to the FCC for approval.
In the Third Report and Order in EB Docket No. 04-296, FCC 11-12,
the Commission adopted rules establishing a regulatory structure for a
national test of the EAS. In order for the Commission to determine the
extent to which the test, and by extension the EAS, was successful, the
FCC adopted rules requiring EAS Participants, within forty five (45)
days of the date of the first national EAS test, to record and submit
to the Commission the following test-related diagnostic information for
each alert received from each message source monitored at the time of
the national test:
Whether they received the alert message during the
designated test;
whether they retransmitted the alert;
if they were not able to receive and/or transmit the
alert, their `best effort' diagnostic analysis regarding the cause(s)
for such failure;
a description of their station identification and level of
designation (PEP, LP-1, etc.);
the date/time of receipt of the EAN message by all
stations; the date/time of PEP station acknowledgement of receipt of
the EAN message to FOC;
the date/time of initiation of actual broadcast of the
Presidential message;
the date/time of receipt of the EAT message by all
stations;
who they were monitoring at the time of the test, and the
make and
model number of the EAS equipment that they utilized.
The Third Report and Order indicates that the national tests of
EAS, and related information collections will likely be carried out on
an annual basis. On March 10, 2010, OMB approved the collection as
indicated by the related Notice of Office of Management and Budget
Action notification.
The FCC is submitting this information collection to the Office of
Management and Budget (OMB) as a revision of the previously approved
information collection that established the mandatory Electronic Test
Reporting System (ETRS) that EAS Participants must utilize to file
identifying and test result data as part of their participation in
nationwide EAS testing. Specifically, the Order adopted in EB Docket
No. 04-296, FCC 16-32, amends the State EAS Plan filing requirements
set forth at Section 11.21 of the Commission's rules to require EAS
Participants (i.e., the broadcasters, cable systems, and other service
providers subject to the FCC's EAS rules) to provide the following
information to their respective SECC, who in turn will include such
information in the State EAS Plan submitted to the Commission for
approval:
A description of any actions taken by the EAS Participant
(acting individually, in conjunction with other EAS Participants in the
geographic area, and/or in consultation with state and local emergency
authorities), to make EAS alert content available in languages other
than English to its non-English speaking audience(s);
A description of any future actions planned by the EAS
Participant, in consultation with state and local emergency
authorities, to provide EAS alert content in languages other than
English to its non-English speaking audience(s), along with an
explanation for the EAS Participant's decision to plan or not plan such
actions; and
Any other relevant information that the EAS Participant
may wish to provide.
In addition, in the event that there is a material change to any of
the information that EAS Participants are required to furnish their
respective SECCs, EAS Participants must, within 60 days of the
occurrence of such material change, submit aa letter to their
respective SECCs, copying the Commission's Public Safety and Homeland
Security Bureau (Bureau) that describe such change. The SECCs are
required to incorporate the information in such letters as amendments
to the State EAS Plans on file with the Bureau.
This information will be used by FCC staff to gauge the
effectiveness of the EAS's capacity to disseminate in-language EAS
emergency alert content to persons who communicate in a language other
than English or may have a limited understanding of the English
language; to determine whether private and local efforts to disseminate
EAS multilingual content might be incorporated into the overall
national EAS structure; and to confirm that private and local EAS
multilingual operations are consistent with national plans, FCC
regulations, and EAS operation.
The Commission expects that the costs to EAS Participants to comply
with these reporting requirements will be minimal, and largely limited
to internal administrative charges associated with drafting a brief
statement, and submitting that statement, and any other relevant
information that the EAS Participant may wish to provide to their SECC
for inclusion into the State EAS Plan for the state in which the EAS
Participant operates. The Commission further expects that the vast
majority of EAS Participants are not engaged in multilingual EAS
activities and therefore will need to submit nothing more than a very
brief statement to their SECC explaining their decision to plan or not
plan future actions to provide EAS alert content in languages other
than English to their non-English speaking audience(s). For the
presumably small percentage of EAS Participants that actually are
engaged in multilingual EAS activities, the filing will merely require
that they supply a summary of actions they already have taken in this
regard. Accordingly, the FCC estimates that complying with the
reporting requirement will take EAS Participants, on average,
approximately one hour. The FCC estimates that compiling the EAS
Participant summaries of multilingual EAS activities and incorporating
such information into the State EAS Plan will take SECCs, on average,
approximately 20 hours.
The following information collection contained in part 11 may be
impacted by these rule amendments: Section 11.21 requires that state
and local EAS plans be reviewed and approved by the Chief, Public
Safety and Homeland Security, prior to implementation to ensure that
they are consistent with national plans, FCC regulations, and EAS
operation.
[[Page 30540]]
Federal Communications Commission.
Marlene H. Dortch,
Secretary.
[FR Doc. 2016-11583 Filed 5-16-16; 8:45 am]
BILLING CODE 6712-01-P