60 day FRN

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Federal Register / Vol. 82, No. 70 / Thursday, April 13, 2017 / Notices

report an average of 15 TA requests per
year.
ATSDR Site Impact Assessment (SIA)
Form: For each environmental health
assessment and health education
activity conducted at ATSDR sites,
awardees must estimate and report the
number of people protected from
exposure to toxic substances at each site
where implementation of agency
recommendations has taken place and at
each child care center where safe siting
guidelines have been implemented. To
the extent possible, awardees must
estimate the disease burden prevented
due to the implementation of site
recommendations and safe siting
guidelines. This information will be
entered into the ATSDR SIA database by
the awardee. ATSDR assumes a

maximum of 150 ATSDR sites will
undergo an environmental assessment,
or an average of six sites per awardee,
per year.
APPLETREE Annual Performance
Report (APR): At the end of each budget
year, awardees must provide an APR,
including an updated Annual Plan of
Work (APOW) for the next budget year.
The report must include a synopsis of
the number of people involved in
environmental health assessments at
sites, the number of public health
recommendations accepted, the number
of health education activities conducted
at sites; and the outcomes achieved
during the budget year. The APR must
also demonstrate annual progress in
implementing child care safe siting
policies in their jurisdictions over the

three-year program period. ATSDR
assumes that APRs will take three
burden hours for each awardee to
prepare.
ATSDR Success Story Form: By the
end of the budget year, each awardee
must also submit a minimum of three
success stories to highlight the
programs’ annual accomplishments.
ATSDR estimates that awardees will
submit an average of four success stories
which will take one hour each to
prepare.
ATSDR seeks a three-year information
collection clearance. Awardee reporting
is a mandatory requirement of the
APPLETREE cooperative agreement.
The total annual time burden requested
is 272 hours.

ESTIMATED ANNUALIZED BURDEN HOURS
Type of
respondents

Form name

APPLETREE Awardees ..........

ATSDR Health Education Activity Tracking (HEAT) Form ....
Technical Assistance (TA) Activity Form ...............................
ATSDR Site Impact Assessment (SIA) Form ........................
APPLETREE Annual Performance Report (APR) .................
Success Story Form ...............................................................

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. 2017–07483 Filed 4–12–17; 8:45 am]
BILLING CODE 4163–70–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

National Institute for
Occupational Safety and Health
(NIOSH), Centers for Disease Control
and Prevention, Department of Health
and Human Services.
ACTION: Notice.
asabaliauskas on DSK3SPTVN1PROD with NOTICES

AGENCY:

NIOSH gives notice of a
decision to evaluate a petition to
designate a class of employees from the
Idaho National Laboratory—Idaho
Chemical Processing Plant in Scoville,
Idaho, to be included in the Special
Exposure Cohort under the Energy
Employees Occupational Illness
Compensation Program Act of 2000.

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FOR FURTHER INFORMATION CONTACT:

Stuart L. Hinnefeld, Director, Division
of Compensation Analysis and Support,
National Institute for Occupational
Safety and Health, 1090 Tusculum
Avenue, MS C–46, Cincinnati, OH
45226–1938, Telephone 877–222–7570.
Information requests can also be
submitted by email to [email protected].
SUPPLEMENTARY INFORMATION:
Authority: 42 CFR 83.9–83.12.

Decision To Evaluate a Petition To
Designate a Class of Employees From
the Idaho National Laboratory—Idaho
Chemical Processing Plant in Scoville,
Idaho, To Be Included in the Special
Exposure Cohort

SUMMARY:

Number of
respondents

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25
25
25
25
25

Average
burden
per response
(in hours)

37
15
6
1
4

3/60
5/60
7/60
3
1

work days within the parameters
established for one or more other classes
of employees in the Special Exposure
Cohort.’’
Period of Employment: January 1,
1975 through December 31, 1980.
John Howard,
Director, National Institute for Occupational
Safety and Health.
[FR Doc. 2017–07474 Filed 4–12–17; 8:45 am]
BILLING CODE 4163–19–P

Pursuant to 42 CFR 83.12, the initial
proposed definition for the class being
evaluated, subject to revision as
warranted by the evaluation, is as
follows:
Facility: Idaho National Laboratory—
Idaho Chemical Processing Plant.
Location: Scoville, Idaho.
Job Titles and/or Job Duties: ‘‘All
employees of the Department of Energy,
its predecessor agencies, and their
contractors and subcontractors who
worked at the Idaho National Laboratory
(INL) in Scoville, Idaho and who were
monitored for external radiation at the
Idaho Chemical Processing Plant (CPP)
with at least one film badge or
thermoluminescent dosimeter from CPP
between January 1, 1975 and December
31, 1980 for a number of work days
aggregating at least 250 work days,
occurring either solely under this
employment, or in combination with

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Number of
responses per
respondent

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60 Day–17–1035; Docket No. CDC–2017–
0022]

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 efforts to reduce public
burden and maximize the utility of
government information, invites the

SUMMARY:

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Federal Register / Vol. 82, No. 70 / Thursday, April 13, 2017 / Notices
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 the proposed information
collection project entitled ‘‘Assessing
School-Centered HIV/STD Prevention
Efforts in a Local Education Agency.’’
This study provides in-depth
assessment of Human
Immunodeficiency Virus (HIV) and
Sexually Transmitted Disease (STD)
prevention efforts in a location
education agency funded by CDC’s
Division of Adolescent and School
Health.
Written comments will be
received on or before June 12, 2017.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2017–
0022 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. 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.
DATES:

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.

asabaliauskas on DSK3SPTVN1PROD with NOTICES

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 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

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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
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
Assessing School-centered HIV/STD
Prevention Efforts in a Local Education
Agency (OMB Control No. 0920–0135;
Expiration 11/30/2017)—Revision—
Division of Adolescent and School
Health (DASH), National Center for
HIV/AIDS, Viral Hepatitis, STD, and TB
Prevention, Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
HIV infections remain high among
young men who have sex with men. The
estimated number of new HIV infections
increased between 2008 and 2010 both
overall and among MSM ages 13 to 24.
Furthermore, sexual risk behaviors
associated with HIV, other STD, and
pregnancy often emerge in adolescence.
For example, 2015 Youth Risk Behavior
Surveillance System (YRBSS) data
revealed 41.2% of U.S. high school
students reported having had sex, and

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17839

among those who had sex in the
previous three months, only 56.9%
reported having used a condom during
last sexual intercourse. In addition,
2015 YRBSS data revealed high school
students identifying as gay, lesbian, and
bisexual and those reporting sexual
contact with both males and females
were more likely to engage in sexual
risk-taking behaviors than heterosexual
students.
Given the disproportionate risk for
HIV among YMSM ages 13–24, it is
important to find ways to reach the
younger youth (i.e., ages 13–19) in this
range to decrease sexual risk behaviors
and increase health-promoting
behaviors such as routine HIV testing.
Schools provide one opportunity for
this. Because schools enroll more than
22 million teens (ages 14–19) and often
have existing health and social services
infrastructure, schools and their staff
members are well-positioned to connect
youth to a wide range of needed
services, including housing assistance,
support groups, and sexual health
services such as HIV testing. As a result,
CDC’s Division of Adolescent and
School Health (DASH) has focused a
number of HIV and STD prevention
efforts on strategies that can be
implemented in or centered on schools.
The CDC requests a one-year approval
to conduct a revised information
collection entitled, ‘‘Assessing SchoolCentered HIV/STD Prevention Efforts in
a Local Education Agency’’ (OMB
Control Number 0920–1035). This
revised information collection request
covers the third in a series of three data
collections; the previous two were
covered under the previously approved
information collection.
The information collection uses a selfadministered paper-pencil
questionnaire, the Youth Health and
School Climate Questionnaire, to assess
HIV and STD prevention efforts in one
local education agency (LEA) funded by
the CDC, Division of Adolescent and
School Health (DASH) under strategy 4
(School-Centered HIV/STD Prevention
for Young Men Who Have Sex with
Men) of PS13–1308: Promoting
Adolescent Health through SchoolBased HIV/STD Prevention and SchoolBased Surveillance.
This data collection will provide data
and reports for the funded LEA, and
will allow the LEA to identify program
areas that are working well and other
areas that need improvement. In
addition, the findings will allow CDC to
determine the potential impact of
currently recommended strategies and
make changes to those
recommendations if necessary. The
questionnaire will include questions on

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Federal Register / Vol. 82, No. 70 / Thursday, April 13, 2017 / Notices

the following topics: demographic
information; HIV and STD risk
behaviors; use of HIV and STD health
services; experiences at school,
including school connectedness,
harassment and bullying, homophobia,
support of Lesbian, Gay, Bisexual,
Transgender, and Queer (LGBTQ)
students; sexual orientation; receipt of
referral for HIV and STD prevention
health services; and health education.
This data collection system involves
administration of a paper-and-pencil
questionnaire to seven high schools that
are participating in the HIV/STD
prevention project of a local education
agency that is funded with support from
CDC’s PS13–1308 cooperative
agreement. The questionnaire, the
Youth Health and School Climate
Questionnaire, will be administered to
approximately 16,500 students across
the seven schools in the 2017–2018

children out of the study. In addition,
each student will be read verbal assent
language that explains he or she may
choose not to take the questionnaire or
may skip any questions in the
questionnaire with no penalty.
Participation is completely voluntary.
The estimated burden per response
ranges from 35–45 minutes. This
variation in burden is due to the slight
variability in skip patterns that may
occur with certain responses and
variations in the reading speed of
students. The burden estimate presented
here is based on the assumption of a 40minute response time per response.
Students will complete the
questionnaire only once under this
approval. Annualizing the collection
over one year results in an estimated
annualized burden of 11,000 hours for
respondents. There are no costs to
respondents other than their time.

school year. This is the third and final
data collection of a four-year project that
includes three data collections; previous
data collections occurred in December
2014 and December 2016. Data
collection points coincide with the
approximate beginning, mid-way, and
end points of the PS13–1308
cooperative agreement. We anticipate
the final data collection will yield data
from up to 16,500 high school students
in grades 9 through 12 at the selected
schools. Although some students may
have completed the questionnaire in
one or more of the previous years, this
is not a longitudinal design and
individual student responses will not be
tracked across the years. No personally
identifiable information will be
collected.
All students’ parents will receive
parental consent forms that provide
them with an opportunity to opt their

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent

Average
burden per
response
(in hours)

Total burden
(in hours)

Form name

Students in grades 9–12 ...................

Youth Health and School Climate
Questionnaire.

16,500

1

40/60

11,000

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

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

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

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

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

11,000

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. 2017–07482 Filed 4–12–17; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2016–N–4389]

Genome Editing in New Plant Varieties
Used for Foods; Extension of
Comment Period
AGENCY:

Food and Drug Administration,

HHS.
Notification; extension of
comment period.

ACTION:
asabaliauskas on DSK3SPTVN1PROD with NOTICES

Number of
respondents

Type of respondents

The Food and Drug
Administration (FDA or we) is
extending the comment period for a
docket to receive information and
comments on the use of genome editing
techniques to produce new plant
varieties that are used for human or
animal food. We established the docket

SUMMARY:

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17:51 Apr 12, 2017

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through a notice that appeared in the
Federal Register of January 19, 2017.
We are taking this action in response to
requests for an extension to allow
interested persons additional time to
submit comments.
DATES: We are extending the comment
period on the notice that published
January 19, 2017 (82 FR 6564). Submit
either electronic or written comments
by June 19, 2017. Late, untimely filed
comments will not be considered. The
https://www.regulations.gov electronic
filing system will accept comments
until midnight Eastern Time at the end
of June 19, 2017. Comments received by
mail/hand delivery/courier (for written/
paper submissions) will be considered
timely if they are postmarked or the
delivery service acceptance receipt is on
or before that date.
ADDRESSES: You may submit comments
as follows:

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.
• 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’’).

Electronic Submissions

Written/Paper 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://

Submit written/paper submissions as
follows:
• Mail/Hand delivery/Courier (for
written/paper submissions): Division of
Dockets Management (HFA–305), Food
and Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.

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