60d FRN - published

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Federal Register / Vol. 82, No. 80 / Thursday, April 27, 2017 / Notices

compelled by law. CDC will retain and
destroy all records in accordance with
the applicable CDC Records Control
Schedule.

OPHPR is requesting an approval
period of one year to collect this
information. There are no cost burdens
to respondents or record keepers for this

data collection. The total time burden to
respondents is 70 hours. See a summary
of the annualized burden hours in the
below table.

ESTIMATED ANNUALIZED BURDEN HOURS
Average
burden per
response
(in hrs.)

Total
burden
(in hrs.)

Form name

Private Sector Organization Senior Leader ..........
Private Sector Organization Manager ..................

Interview Plan ...............
Survey Plan ..................

45
100

1
1

1
15/60

45
25

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

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

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

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

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

70

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. 2017–08540 Filed 4–26–17; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day-17–17ABU; Docket No. CDC–2017–
0037]

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
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 a proposed data collection
project titled ‘‘Emergency Zika Package:
Zika Reproductive Health Call-Back
Survey ZRHCS), 2017.’’
DATES: Written comments must be
received on or before June 26, 2017.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2017–
0037 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,
SUMMARY:

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Number of
responses per
respondent

Number of
respondents

Type of respondents

VerDate Sep<11>2014

17:07 Apr 26, 2017

Jkt 241001

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.
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 Leroy A.
Richardson, Information Collection
Review Office, Centers for Disease
Control and Prevention, 1600 Clifton
Road NE., MS–D74, Atlanta, Georgia
30329; phone: 404–639–7570; Email:
omb@cdc.gov.
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

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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
Zika Reproductive Health Call-Back
Survey (ZRHCS), 2017—New—National
Center for Chronic Disease Prevention
and Health Promotion (NCCDPHP),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
In May 2015, the World Health
Organization reported the first local
mosquito born transmission of Zika
virus in the Western Hemisphere, with
autochthonous cases identified in
Brazil. In response to the Zika virus
outbreak, and evidence that Zika virus
infection during pregnancy is a cause

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Federal Register / Vol. 82, No. 80 / Thursday, April 27, 2017 / Notices
microcephaly and other adverse
pregnancy and infant outcomes, CDC’s
Emergency Operations Center has
continued to work at the highest level
of activation since February 8, 2016. To
date, local transmission has been
identified in at least 50 countries or
territories in the Americas; within the
United States, widespread mosquito
born transmission has been documented
in the territories of Puerto Rico and the
US Virgin Islands, and more localized
transmission has been observed in
Florida and Texas. In addition in the
continental United States, there has
been a large number of travel-related
cases with infection occurring through
mosquito born and sexual transmission.
Given the adverse pregnancy and
birth outcomes associated with Zika
virus infection during pregnancy,
increasing access to effective
contraception is a key countermeasure
for preventing unintended pregnancies
that might otherwise be affected by
Zika. In addition, even in the absence of
disease outbreaks that can lead to
negative pregnancy and birth outcomes,
access to contraception is needed to
help prevent the 45% of pregnancies in
the United States that are unintended.
Given that the proportion of pregnancies

to Zika areas and knowledge of and
adherence to travel recommendations.
The 14 jurisdictions included have had
widespread local transmission, are at
high risk for local transmission, and/or
have a disproportionately high number
of travel-related cases.
The information collected will be
provided to state and territory health
departments to provide a basis on which
to develop emergency response plans
for potential outbreaks and make
decisions regarding the distribution of
finite resources to prevent Zika virus
infection during pregnancy. Given the
potential for new outbreaks and
increases in cases in areas with Zika as
the summer travel and mosquito season
approaches, an interim data set and
report would be made available to states
no later than June, 2017. Additionally,
in the event that a jurisdiction has an
increase in Zika cases or newly reported
local transmission, interim data will be
analyzed and provided within 10
business days to aid in emergency
response planning.
Participation is voluntary and there
are no costs to respondents other than
their time.

that are unintended varies widely across
states, it is important to identify
populations with high unmet need for
contraception to implement targeted
strategies for increasing access to and
availability of effective contraception.
Additionally, it is important for women
who are at risk of becoming pregnant
unintentionally, or who are planning a
pregnancy, to be knowledgeable of
behaviors for preventing mosquito born
and sexual transmission of Zika and
recommendations for waiting to get
pregnant after they or their partner have
returned from an area with Zika.
The objective of this assessment is to
collect scientifically valid, current
information on various aspects of Zika
knowledge and prevention behaviors
from a representative sample of adult
women of reproductive age (aged 18–49
years) in 14 states/territories, including
information: (1) The use of
contraception among women wishing to
avoid or delay pregnancies that might
otherwise be affected by Zika; (2)
barriers to access and use of
contraception; (3) knowledge of and
adherence to mosquito prevention
strategies and use of condoms to
minimize the risk of sexual
transmission; and (4) frequency of travel

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents

Type of respondents

Form name

Women aged 18–49 years who completed the main BRFSS survey.
Women aged 18–49 years from
areas with local Zika transmission.
Women aged 18–49 years from
areas where travel related Zika
predominates.
State BRFSS Coordinators ...............

Recruitment text ...............................

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

Call-back
Version
Call-back
Version

14,508

1

1/60

242

2,000

1

10/60

333

and

Consent,

12,000

1

12/60

2,400

Data Submission Layout ..................

14

8

3

336

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

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

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

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

3,311

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–17–0879; Docket No. CDC–2017–
0044]

mstockstill on DSK30JT082PROD with NOTICES

BILLING CODE 4163–18–P

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

SUMMARY:

17:07 Apr 26, 2017

Total burden
hours

Consent,

[FR Doc. 2017–08493 Filed 4–26–17; 8:45 am]

VerDate Sep<11>2014

Average
burden
per response
(in hrs.)

and

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.

Survey
A.
Survey
B.

Number of
responses per
respondent

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PO 00000

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Fmt 4703

Sfmt 4703

its continuing effort 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 the information collection
project titled ‘‘Information Collections
to Advance State, Tribal, Local and
Territorial (STLT) Governmental
Agency and System Performance,
Capacity, and Program Delivery.’’
Information, collected across a range of
public health topics using standard
modes of administration (e.g., web, in-

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