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Federal Register / Vol. 84, No. 176 / Wednesday, September 11, 2019 / Notices
adulthood in the healthiest possible
way.
CDC will use a web-based system to
collect data on the approaches that
LEAs are using to meet their goals.
Approaches include helping LEAs and
priority schools deliver sexual health
education emphasizing HIV and other
STD prevention; increasing adolescent
access to key sexual health services; and
establishing safe and supportive
environments for students and staff. To
track LEA progress and evaluate the
effectiveness of program activities, CDC
will be collecting data using a mix of
process and outcome measures. Process
measures to be completed by all LEAs
will assess the extent to which planned
program activities have been
implemented and lead to feasible and
sustainable programmatic outcomes.
Process measures include items on
school health policy and practice
assessment and training and technical
assistance received from nongovernmental partner organizations.

Outcome measures, which will be
completed by local education agencies,
assess whether funded activities at each
site are leading to intended outcomes
including public health impact of
systemic change in schools. These
measures drove the development of
questionnaires that have been tailored to
each of the LEAs’ strategies (i.e., SHE,
SHS, SSE).
Respondents are 25 LEAs that have
been funded under PS18–1807. Local
education agencies will complete the
questionnaires semi-annually using the
Program Evaluation and Reporting
System (PERS), an electronic web-based
interface specifically designed for this
data collection. Each LEA will receive a
unique log-in to the system and
technical assistance to ensure they can
use the system easily. The dates when
data are requested reflect the Office of
Financial Resources (OFR) deadlines to
provide timely feedback to LEAs and
CDC staff for accountability and optimal
use of funds. CDC anticipates that semi-

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annual information collection will begin
in February 2020 and will describe
activities conducted during the period
August 2019–July 2022. The estimated
burden per response is approximately
2–26 hours. This estimate includes time
for local education agencies to gather
information at the district and schoollevels. Annualizing this collection over
three years results in an estimated
annualized burden of 1,750 hours per
year and 5,250 for three years across all
funded local education agencies.
LEAs are required to allocate at least
6% of their NOFO award on evaluation
ranging from $15,000 to $21,000.
Grantees may use these discretionary
funds for collection of process and
outcome measures, including time to
gather and enter data into the online
and evaluation reporting system. There
is no cost to the respondents other than
their time. The total annual burden
hours are 1,750.

ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents

Form name

Number of
respondents

Number of
responses per
respondent

Average
burden per
response
(in hours)

LEA .........................................

Funded District Questionnaire ................................................
Priority School Questionnaire .................................................
District Assistance Questionnaire ...........................................

25
25
25

2
2
2

2
26
7

Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2019–19631 Filed 9–10–19; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30-Day–19–1202]

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Agency Forms Undergoing Paperwork
Reduction Act Review
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled Survey of
Engineered Nanomaterial Occupational
Safety and Health Practices to the Office
of Management and Budget (OMB) for
review and approval. CDC previously
published a ‘‘Proposed Data Collection
Submitted for Public Comment and
Recommendations’’ notice on April 23,
2019, to obtain comments from the

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public and affected agencies. CDC did
not receive comments related to the
previous notice. This notice serves to
allow an additional 30 days for public
and affected agency comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
(a) 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;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
(d) 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,

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e.g., permitting electronic submission of
responses; and
(e) Assess information collection
costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570 or
send an email to omb@cdc.gov. Direct
written comments and/or suggestions
regarding the items contained in this
notice to the Attention: CDC Desk
Officer, Office of Management and
Budget, 725 17th Street NW,
Washington, DC 20503 or by fax to (202)
395–5806. Provide written comments
within 30 days of notice publication.
Proposed Project
Survey of Engineered Nanomaterial
Occupational Safety and Health
Practices (OMB Control No. 0920–1202,
Exp. 10/31/2019)—Revision—National
Institute for Occupational Safety and
Health (NIOSH), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
As mandated in the Occupational
Safety and Health Act of 1970 (Pub. L.
91–596), the mission of the National

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Federal Register / Vol. 84, No. 176 / Wednesday, September 11, 2019 / Notices

Institute for Occupational Safety and
Health (NIOSH) is to conduct research
and investigations on work-related
disease and injury and to disseminate
information for preventing identified
workplace hazards (Sections 20(a)(1)
and (d)). This dual responsibility
recognizes the need to translate research
into workplace application if it is to
impact worker safety and well-being.
The goal of this project is to assess the
relevance and impact of NIOSH’s
contribution to guidelines and risk
mitigation practices for safe handling of
engineered nanomaterials in the
workplace. The intended use of this
data is to inform NIOSH’s research
agenda to enhance its relevance and
impact on worker safety and health in
the context of engineered nanomaterials.
The research under this project will
survey companies who manufacture,
distribute, fabricate, formulate, use or
provide services related to engineered

nanomaterials. The analysis will
describe the survey sample, response
rates, and types of company by industry
and size. Further analysis will focus on
identifying the types of engineered
nanomaterials being used in industry
and the types of occupational safety and
health practices being implemented.
The analysis will be used to develop a
final report which evaluates the
influence of NIOSH products, services,
and outputs on industry occupational
safety and health practices.
Under this project, the following
activities and data collections will be
conducted:
(1) Company Pre-calls. Sampled
companies will be contacted to identify
the person who will complete the
survey and to ascertain whether or not
the company handles engineered
nanomaterials.
(2) Survey. A web-based
questionnaire, with a mail option, will

be administered to companies. The
purpose of the survey is to learn directly
from companies about their use of
NIOSH materials and their occupational
safety and health practices concerning
engineered nanomaterials.
A sample of 600 companies will be
compiled from lists of industry
associations, research reports, marketing
databases, and web-based searches. Of
the 600 selected companies we
anticipate that 500 will complete the
survey. The company pre-call is
expected to require five minutes to
complete. The survey is expected to
require 20 minutes to complete;
including the time it may take
respondents to look-up and retrieve
needed information. The estimated
annualized burden hours for the
respondents’ time to participate in this
information collection is 108 hours.
There are no costs to the responders
other than their time.

ESTIMATED ANNUALIZED BURDEN HOURS
Form name

Receptionist ............................................................................
Occupational health and safety specialists .............................
Industrial Production Managers ..............................................
Natural Sciences Managers ....................................................

Pre-call ...................................
Survey ....................................
Survey ....................................
Survey ....................................

Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2019–19633 Filed 9–10–19; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers CMS–10261, CMS–
10556, CMS–R–305, CMS–10328 and CMS–
10079]

Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, HHS.
ACTION: Notice.
AGENCY:

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Number of
respondents

Type of respondents

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
(PRA), federal agencies are required to
publish notice in the Federal Register

SUMMARY:

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concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, and to allow
a second opportunity for public
comment on the notice. Interested
persons are invited to send comments
regarding the burden estimate or any
other aspect of this collection of
information, including the necessity and
utility of the proposed information
collection for the proper performance of
the agency’s functions, the accuracy of
the estimated burden, ways to enhance
the quality, utility, and clarity of the
information to be collected, and the use
of automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
DATES: Comments on the collection(s) of
information must be received by the
OMB desk officer by October 11, 2019.
ADDRESSES: When commenting on the
proposed information collections,
please reference the document identifier
or OMB control number. To be assured
consideration, comments and
recommendations must be received by
the OMB desk officer via one of the
following transmissions: OMB, Office of
Information and Regulatory Affairs,

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300
100
75
75

Number of
responses per
respondent
1
1
1
1

Avg. burden
per response
(in hrs.)
5/60
20/60
20/60
20/60

Attention: CMS Desk Officer, Fax
Number: (202) 395–5806 OR Email:
OIRA_submission@omb.eop.gov.
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 following:
1. Access CMS’ website address at
website address at https://www.cms.gov/
Regulations-and-Guidance/Legislation/
PaperworkReductionActof1995/PRAListing.html.
1. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov.
2. Call the Reports Clearance Office at
(410) 786–1326.
FOR FURTHER INFORMATION CONTACT:
William Parham at (410) 786–4669.
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. 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

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