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Federal Register / Vol. 81, No. 80 / Tuesday, April 26, 2016 / Notices

primary Federal agency for protecting
health and promoting quality of life
through the prevention and control of
disease, injury, and disability. The CDC
Workplace Health Promotion Resource
Center is authorized by the Public
Health Service Act and funded through
the Prevention and Public Health Fund
of the Patient Protection and Affordable
Care Act (ACA).
Resource Center development and
information collection will be
conducted in two phases over a threeyear period. In Phase 1 (project years 1
and 2), CDC will conduct formative
research to understand the needs and
preferences of the target audience. In
Phase 2 (project years 2 and 3), CDC will
build the Resource Center and IC,
provide technical assistance, and assess
customer satisfaction.

During Phase 1, CDC will conduct
telephone interviews with 50
individuals who represent key Resource
Center audiences: Employers (N=10),
business groups (N=10), vendors and
consultants (N=12), public health
organizations (N=4), journalists (N=4),
and researchers (N=10). Each tailored
interview will be 45–60 minutes in
length. Additional information will be
collected through an online Needs and
Interests Market Survey involving 800
respondents. Findings will be used to
tailor the contents, technical support
and dissemination practices of the
Resource Center to the needs and
interests of the target audiences.
During Phase 2, Resource Center
products will be launched and CDC will
collect brief, online customer
satisfaction surveys from approximately

850 users. CDC will also pilot test and
evaluate a direct technical assistance
component of the Resource Center with
approximately 5 selected states using
two online surveys: a TA feedback
survey and TA pilot assessment. The TA
feedback survey will be offered to up to
100 stakeholders after each TA
encounter and will take approximately
5 minutes. The TA pilot assessment will
be provided at the conclusion of the TA
pilot to up to 100 stakeholders and will
take approximately 20 minutes.
Findings will be used to improve
workplace health programs and the
offerings of the Resource Center.
OMB approval is requested for three
years. Participation is voluntary and
there are no costs to respondents other
than their time.

ESTIMATED ANNUALIZED BURDEN HOURS
Form name

Employers .............................................

Technical Assistance ............................
(TA) Participants ...................................

Needs and Interests Interview Guide
for Employers.
Needs and Interests Interview Guide
for Business Groups, Vendors, Consultants, and Public Health Organizations.
Needs and Interests Interview Guide
for Journalists.
Needs and Interests Interview Guide
for the Research Community.
Stakeholder Needs and Interests Market Survey.
Consumer Satisfaction Survey .............
TA Feedback Survey ...........................
TA Pilot Assessment ............................

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

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

Business Groups, Vendors, Consultants, and Public Health Organizations.
Journalists .............................................
Researchers ..........................................
Key Stakeholders and Users of the Resource Center (All Groups).

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. 2016–09638 Filed 4–25–16; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES

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Centers for Disease Control and
Prevention
[60Day-16–0199; Docket No. CDC–2016–
0039]

Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).

AGENCY:

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ACTION:

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Total
burden
(in hrs.)

1

1

3

9

1

1

9

1

1

45/60

1

3

1

45/60

2

267

1

20/60

89

283
33
33

1
5
1

2/60
5/60
20/60

9
14
11

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

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

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

138

The Centers for Disease
Control and Prevention (CDC), as part of
its continuing efforts to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies to take this opportunity to
comment on proposed and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on an extension request for
the information collection entitled
Application for Permit to Import
Biological Agents and Vectors of Human
Disease into the United States and
Application for Permit to Import or
Transport Live Bats (42 CFR 71.54).
DATES: Written comments must be
received on or before June 27, 2016.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2016–
0039 by any of the following methods:

Frm 00063

Average
burden per
response
(in hrs.)

3

Notice with comment period.

SUMMARY:

PO 00000

Number of
responses per
respondent

Number of
respondents

Type of respondents

• Federal eRulemaking Portal:
Regulation.gov. Follow the instructions
for submitting comments.
• Mail: Leroy A. Richardson,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road, NE.,
MS–D74, Atlanta, Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. All relevant comments
received will be posted without change
to Regulations.gov, including any
personal information provided. For
access to the docket to read background
documents or comments received, go to
Regulations.gov.
Please note: All public comment should be
submitted through the Federal eRulemaking
portal (Regulations.gov) or by U.S. mail to the
address listed above.

To
request more information on the
proposed project or to obtain a copy of

FOR FURTHER INFORMATION CONTACT:

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Federal Register / Vol. 81, No. 80 / Tuesday, April 26, 2016 / Notices
the information collection plan and
instruments, contact the Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road, NE., MS–D74, Atlanta,
Georgia 30329; phone: 404–639–7570;
Email: [email protected].
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires Federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology; and (e) estimates of capital
or start-up costs and costs of operation,
maintenance, and purchase of services
to provide information. Burden means
the total time, effort, or financial
resources expended by persons to
generate, maintain, retain, disclose or
provide information to or for a Federal

materials to obtain a permit issued by
the CDC.
CDC requests Office of Management
and Budget approval to collect
information for three years using the
Application for Permit to Import
Infectious Biological Agents into the
United States and the Application for a
Permit to Import or Transport Live Bats.
The Application for Permit to Import
Biological Agents, Infectious Substances
and Vectors of Human Disease into the
United States form is used by laboratory
facilities, such as those operated by
government agencies, universities, and
research institutions to request a permit
for the importation of biological agents,
infectious substances, or vectors of
human disease. This form currently
requests applicant and sender contact
information; description of material for
importation; facility isolation and
containment information; and personnel
qualifications. CDC plans to make no
changes to this application.
The Application for Permit to Import
or Transport Live Bats form is used by
laboratory facilities such as those
operated by government agencies,
universities, research institutions, and
for educational, exhibition, or scientific
purposes to request a permit for the
importation, and any subsequent
distribution after importation, of live
bats. This form currently requests the
applicant and sender contact
information; a description and intended
use of bats to be imported; and facility
isolation and containment information.
CDC plans to make no changes to this
application.
Estimates of burden for the survey are
based on information obtained from the
CDC import permit database on the
number of permits issued on annual
basis since 2010. The total estimated
burden for the one-time data collection
is 545 hours.
There are no costs to respondents
except their time.

agency. This includes the time needed
to review instructions; to develop,
acquire, install and utilize technology
and systems for the purpose of
collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information; and to
transmit or otherwise disclose the
information.
Proposed Project
Application for Permit to Import
Biological Agents and Vectors of Human
Disease into the United States and
Application for Permit to Import or
Transport Live Bats (42 CFR 71.54)
(OMB Control No. 0920–0199, exp. 01/
31/2017)—Extension—Office of Public
Health Preparedness and Response
(OPHPR), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
Section 361 of the Public Health
Service Act (42 U.S.C. 264), as
amended, authorizes the Secretary of
Health and Human Services to make
and enforce such regulations as are
necessary to prevent the introduction,
transmission, or spread of
communicable diseases from foreign
countries into the States or possessions,
or from one State or possession into any
other State or possession. Part 71 of
Title 42, Code of Federal Regulations
(Foreign Quarantine) sets forth
provisions to prevent the introduction,
transmission, and spread of
communicable disease from foreign
countries into the United States.
Subpart F—Importations—contains
provisions for the importation of
infectious biological agents, infectious
substances, and vectors (42 CFR 71.54);
requiring persons that import these

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ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents

Number
responses per
respondent

Average
burden per
response
(in hours)

Total
burden
hours

Type of respondent

Form name

Applicants Requesting to Import Biological Agents, Infectious Substances
and Vectors.

1,625

1

20/60

542

Applicants Requesting to Import Live
Bats.

Application for Permit to Import Biological Agents, Infectious Substances and Vectors of Human Disease into the United States.
Application for a Permit to Import Live
Bats.

10

1

20/60

3

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

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

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

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

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

545

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Federal Register / Vol. 81, No. 80 / Tuesday, April 26, 2016 / 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. 2016–09657 Filed 4–25–16; 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
Title: Child Care Development Fund
Plan for Tribes for FFY 2017–2019
(ACF–118–A).
OMB No.: 0970–0198.
Description: The Child Care and
Development Fund (CCDF) Plan (the
Plan) for Tribes is required from each
CCDF Lead Agency in accordance with
Section 658E of the Child Care and
Development Block Grant (CCDBG) Act,
as amended, by Public Law 113–186

and U.S.C. 9858. The Plan provides ACF
and the public with a description of,
and assurances about, the Tribes’ child
care program.
The FY 2017–2019 CCDF Plan
Preprint for Tribal grantees is being
published in the Federal Register for a
30-day Public Comment Period to
provide an opportunity for the public to
submit comments to the Office of
Management and Budget (OMB). The
first 60-day comment period on the
Tribal Preprint closed on March 19,
2016. The Office of Child Care (OCC)
has given thoughtful consideration to
those comments received during the 60day Public Comment Period. The Plan
has been revised to provide additional
guidance and clarification throughout
the document to improve the quality of
the information requested. Additional
revisions were also made to identify
those questions related to the CCDBG
Act of 2014 that were added for
‘‘informational purposes only’’. A red
delta sign has been inserted to
specifically identify those questions
related to the new law. The CCDBG Act
of 2014, signed into law in November of

2014 made significant changes to the
CCDF program. However, the law did
not explicitly indicate the extent to
which many of the new requirements
apply to Tribes. Questions related to the
CCDBG Act of 2014 will provide ACF
with baseline information on Tribal
practices and technical assistance
needs.
ACF extended the current Tribal Plan
for one year, which means that Tribes
will submit new 3-year Plans for FY
2017–2019 on July 1, 2016, with an
effective date of October 1, 2016. This
additional time allowed the Office of
Child Care to consult with Tribal
Leaders and their designated
representatives to solicit input on how
the new requirements of the CCDBG Act
of 2014 might apply to Tribal child care
programs. HHS will publish a Final
Rule to determine the extent to which
the new law applies to Tribes. Pending
the issuance of new regulations and
guidance, Tribes are subject to the prior
law and regulations.
Respondents: Tribal CCDF Lead
Agencies (257).

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ANNUAL BURDEN ESTIMATES
Instrument

Number of
respondents

Number of
responses per
respondent

Average
burden hours
per response

Total burden
hours

ACF–118–A .....................................................................................................

257

0.50

120

15,420

Estimated Total Annual Burden
Hours: 15,420.
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 title
of the information collection. Email
address: [email protected].
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
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_
[email protected], Attn:

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Desk Officer for the Administration for
Children and Families.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2016–09618 Filed 4–25–16; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: State Access and Visitation
Grant Application.
OMB No.: 0970—NEW.
Description
The Personal Responsibility and Work
Opportunity Reconciliation Act of 1996
(PRWORA) created the ‘‘Grants to States
for Access and Visitation’’ program (AV
grant program). Funding for the program
began in FY 1997 with a capped, annual
entitlement of $10 million. The
statutory goal of the program is to

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provide funds to states that will enable
them to provide services for the purpose
of increasing noncustodial parent (NCP)
access to and visitation with their
children. State governors decide which
state entity will be responsible for
implementing the AV grant program and
the state determines who will be served,
what services will be provided, and
whether the services will be statewide
or in local jurisdictions. The statute
specifies certain activities which may be
funded, including: voluntary and
mandatory mediation, counseling,
education, the development of parenting
plans, supervised visitation, and the
development of guidelines for visitation
and alternative custody arrangements.
Even though OCSE manages this
program, the funding for the AV grant
is separate from funding for federal and
state administration of the Child
Support program.
Section 469B(e)(3) of the Social
Security Act (Pub. L. 104–193) requires
that each state receiving an Access and
Visitation (AV) grant award monitor,
evaluate and report on such programs in
accordance with regulations (45 CFR
part 303). The AV Grant Program Terms

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