60 day FRN

Federal Register / Vol. 83, No. 111 / Friday, June 8, 2018 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–18–0969; Docket No. CDC–2018–
0044]

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 effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies the opportunity to comment on
a proposed and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled Monitoring Changes in Attitudes
and Practices among Family Planning
Providers and Clinics. This project seeks
to obtain information on changes in
attitudes and practices among family
planning providers and clinics in the
United States related to
recommendations from national
contraception guidelines.
DATES: CDC must receive written
comments on or before August 7, 2018.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2018–
0044 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, 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. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
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

amozie on DSK3GDR082PROD with NOTICES1

SUMMARY:

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Jkt 241001

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 the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. 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;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected; and
4. 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,
e.g., permitting electronic submissions
of responses.
5. Assess information collection costs.
Proposed Project
Monitoring Changes in Attitudes and
Practices among Family Planning
Providers and Clinics (OMB No. 0920–
0969, exp. 5/31/2014)—Reinstatement
with Change—National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
The Division of Reproductive Health
(DRH) at the Centers for Disease Control
and Prevention (CDC) and the HHS
Office of Population Affairs (OPA)
develop and disseminate guidance to
improve the use of contraception and
the delivery of quality family planning
services. The U.S. Medical Eligibility

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26687

Criteria for Contraceptive Use (US
MEC), the first national guidance on
family planning containing evidencebased recommendations for the safe use
of contraceptive methods for women
and men with specific characteristics
and medical conditions, was first
published by the CDC in June 2010. The
US Selected Practice Recommendations
for Contraceptive Use (US SPR), which
provides guidance on how to use
contraceptive methods safely and
effectively once they are deemed to be
medically appropriate, was first
published by the CDC in June 2013. The
US MEC and US SPR were updated after
review of the scientific evidence and
consultation with national experts in
family planning; the revised US MEC
and US SPR were published in August
2016. Providing Quality Family
Planning Services (QFP), which
provides evidence-informed
recommendations to improve client care
and service delivery infrastructure to
support the provision of quality family
planning services to women and men of
reproductive age in the United States,
was published by CDC and OPA in
April 2014. The US MEC, US SPR, and
QFP have been widely disseminated to
health care providers and other
constituents via professional
organizations, federal program grantees,
scientific and programmatic meetings,
scientific manuscripts, online resources,
and other avenues.
To monitor changes in attitudes and
practices regarding provision of
contraception among family planning
providers and clinics, we initiated a
multi-phase assessment. In 2009–2010,
CDC carried out the first phase of the
assessment, collecting information
before the release of the US MEC (OMB
No. 0920–0008). In 2013–2014, CDC, in
collaboration with OPA, carried out the
second phase of the assessment,
collecting information before the release
of the US SPR and QFP (OMB No. 0920–
0969). These information collections
provided useful knowledge about
attitudes and practices of family
planning providers. CDC and OPA used
the findings to develop educational
materials and opportunities for health
care providers.
In 2018, in collaboration with OPA,
CDC plans to request a reinstatement of
OMB No. 0920–0969, ‘Monitoring
Changes in Attitudes and Practices
among Family Planning Providers and
Clinics’ to carry out the third phase of
the assessment. As in the previous
phases, the information collection will
allow CDC and OPA to improve family
planning-related practice by: (1)
Understanding the current use of
contraception guidance in practice,

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26688

Federal Register / Vol. 83, No. 111 / Friday, June 8, 2018 / Notices

including awareness and use of the US
MEC, US SPR and QFP; (2) describing
current attitudes and practices among
family planning providers and clinics
related to recommendations included in
the US MEC, US SPR, and QFP and
assessing changes from previous data
collections; and (3) identifying training
needs in use of guidance and family
planning service delivery (e.g., provider
tools, continuing education modules).
As in previous phases of data
collection, CDC plans to administer

formatting, usability, and data quality.
OMB approval is requested for one year.
The estimated burden per response for
providers is 15 minutes and has not
changed since the previous OMB
approval. The estimated burden per
response for administrators will be
reduced from 40 minutes to 35 minutes.
The total burden for participants is
estimated at 1,916 hours. Participation
is voluntary and there are no costs to
respondents other than their time.

surveys to private and public sector
family planning providers and clinic
administrators in the United States. The
design, methodology, and analytic
approach that CDC plans to implement
are based on methods previously
approved for the 2013–2014 survey,
with different instruments being
administered to providers and clinic
administrators. Minor changes to survey
content will be made to eliminate
unnecessary questions, add new
questions of interest, and improve

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent

Average
burden per
response
(in hours)

Total burden
(in hours)

Form name

Office-based physicians (private sector).

2018–2019 Survey of Health Care
Providers about Family Planning
Attitudes and Practices.
2018–2019 Survey of Health Care
Providers about Family Planning
Attitudes and Practices.
2018–2019 Survey of Health Care
Providers about Family Planning
Attitudes and Practices.
2018–2019 Survey of Administrators
of Health Centers that Provide
Family Planning.
2018–2019 Survey of Administrators
of Health Centers that Provide
Family Planning.

1,000

1

15/60

250

1,000

1

15/60

250

1,000

1

15/60

250

1,000

1

35/60

583

1,000

1

35/60

583

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

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

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

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

1,916

Title X clinic providers (public sector)
Non-Title X publicly funded clinic
providers (public sector).
Title X clinic administrators (public
sector).
Non-Title X publicly funded clinic administrators (public sector).
Total ...........................................

Jeffrey M. Zirger,
Acting 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. 2018–12373 Filed 6–7–18; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–18–18ACN; Docket No. CDC–2018–
0042]

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:
amozie on DSK3GDR082PROD with NOTICES1

Number of
respondents

Type of respondents

The Centers for Disease
Control and Prevention (CDC), as part of
its continuing effort to reduce public
burden and maximize the utility of
government information, invites the

SUMMARY:

VerDate Sep<11>2014

16:53 Jun 07, 2018

Jkt 241001

general public and other Federal
agencies the opportunity to comment on
a proposed and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled Undetermined cause of Serratia
marcescens infections—Multiple States,
2018. The goal of this investigation is to
identify potential risk factors leading to
an outbreak of Serratia marcescens
infections among U.S. healthcare
patients. Data will be used to identify a
cause of the infections and prevent
additional events from occurring.
DATES: CDC must receive written
comments on or before August 7, 2018.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2018–
0042 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, 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

PO 00000

Frm 00048

Fmt 4703

Sfmt 4703

Docket Number. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
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

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