60 day FRN

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Federal Register / Vol. 82, No. 238 / Wednesday, December 13, 2017 / Notices
focus group discussion. DCPC has
developed a set of example questions
that can be used to develop a discussion
guide for each focus group activity. The
average burden for response for each
focus group will be two hours. DCPC
has also developed a set of example
questions that can be tailored to screen

the activity and include the customized
information collection instruments.
OMB approval is requested for three
years. There are no changes to
information collection purpose or
methodology. Participation is voluntary
and there are no costs to respondents
except their time.

for targeted groups of respondents. The
average burden per response for
screening and recruitment is three
minutes.
A separate information collection
request will be submitted to OMB for
approval of each focus group activity.
The request will describe the purpose of

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent

Average
burden per
response
(in hours)

Total burden
(in hours)

Form name

General Public ..................................
General Public ..................................
Health Care Professionals ................
Health Care Professionals ................

Screening Form ................................
Focus Group Guide ..........................
Screening Form ................................
Focus Group Guide ..........................

960
480
640
320

1
6
1
1

3/60
2
3/60
2

48
960
32
640

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

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

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

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

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

1,680

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. 2017–26783 Filed 12–12–17; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention

Proposed Data Collections 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 the National Vital Statistics Report
Forms. These are the data collection
forms used by State and/or county vital
registration offices to report to the
Federal government (a) provisional
counts of births, deaths, and infant
deaths at the end of each month and (b)
annual counts of marriages and

SUMMARY:

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18:53 Dec 12, 2017

Jkt 244001

divorces/annulments in support of the
National Vital Statistics System. This
submission contains no changes to the
actual data collection forms. However,
the number of respondent for the
monthly and annual forms have shifted
from 91 and 58 respectively to 58 and
91, since the 33 New Mexico Counties
only send marriage and divorce
information that is now only captured
in the annual report.
DATES: CDC must receive written
comments on or before February 12,
2018.
You may submit comments,
identified by Docket No. CDC–2017–
0107 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. 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.
ADDRESSES:

[60Day–18–0213, Docket No. CDC–2017–
0107]

sradovich on DSK3GMQ082PROD with NOTICES

Number of
respondents

Type of respondent

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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.

SUPPLEMENTARY INFORMATION:

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58608

Federal Register / Vol. 82, No. 238 / Wednesday, December 13, 2017 / Notices

Proposed Project
National Vital Statistics Report Forms
(OMB Control Number 0920–0213,
expires 04/30/2018)—Revision—
National Center for Health Statistics
(NCHS), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The compilation of national vital
statistics dates back to the beginning of
the 20th century and has been
conducted since 1960 by the Division of
Vital Statistics of the National Center for
Health Statistics, CDC. The collection of
the data is authorized by 42 U.S.C. 242k.
This submission requests approval to
collect the monthly and annually
summary statistics for three years.

immediately following the month of
occurrence.
The Annual Vital Statistics
Occurrence Report Form collects final
annual counts of marriages and divorces
by month for each State and Territory,
the District of Columbia, and New York
City as well as 33 counties in New
Mexico. These final counts are usually
available from State or county officials
about eight months after the end of the
data year. The data are widely used by
government, academic, private research,
and commercial organizations in
tracking changes in trends of family
formation and dissolution.
There are no costs to respondents
other than their time.

The Monthly Vital Statistics Report
forms provide counts of monthly
occurrences of births, deaths, and infant
deaths. Similar data have been
published since 1937 and are the sole
source of these data at the National
level. The data are used by the
Department of Health and Human
Services and by other government,
academic, and private research and
commercial organizations in tracking
changes in trends of vital events.
Respondents for the Monthly Vital
Statistics Reports Form are registration
officials in each State and Territory, the
District of Columbia, and New York
City. This form is also designed to
collect counts of monthly occurrences of
births, deaths, and infant deaths

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent

Average
burden per
response
(in hours)

Total burden
(in hours)

Form name

State, Territory, and other officials ...
State, Territory, and New Mexico
County Officials.

Monthly Vital Statistics Report .........
Annual Vital Statistics Occurrence
Report.

58
91

12
1

8/60
30/60

93
46

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

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

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

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

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

139

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. 2017–26782 Filed 12–12–17; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–17–1054]

Agency Forms Undergoing Paperwork
Reduction Act Review

sradovich on DSK3GMQ082PROD with NOTICES

Number of
respondents

Type of respondents

In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled Drug Overdose
Response Investigation (DORI) Data
Collections 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 July, 17,
2017 to obtain comments from the
public and affected agencies. CDC
received 10 comments related to the
previous notice. This notice serves to

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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,
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

PO 00000

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Fmt 4703

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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
Drug Overdose Response Investigation
(DORI) Data Collections (OMB Control
Number 0920–1054, Expiration 03/31/
2018)—Extension—National Center for
Injury Prevention and Control (NCIPC),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
In 2015, CDC received a three-year
OMB approval (OMB Control Number
0920–1054) for a new generic clearance
plan to collect information in response
to urgent requests from state and local
health authorities to provide
epidemiological information that allows
for the selection of interventions to curb
local epidemics of drug overdose. CDC
seeks OMB approval for an extension of
this generic clearance plan for another
three-year period.
Drug Overdose Response Investigation
(DORI) are to be conducted in response
to urgent requests from state and local
health authorities to provide

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