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Federal Register / Vol. 82, No. 3 / Thursday, January 5, 2017 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Average
burden per
response
(in hours)

Total burden
(in hours)

Form name

General Population ............................
Adults Smokers and Nonsmokers,
ages 18–54, in the United States.

Screening & Consent Questionnaire
Smoker Survey (Wave A) ................

25,000
6,500

1
1

5/60
30/60

2,084
3,250

Smoker Survey (Wave B) ................
Smoker Survey (Wave C) ................
Smoker Survey (Wave D) ................
Smoker Survey (Wave E) ................
Nonsmoker Survey (Wave A) ..........
Nonsmoker Survey (Wave B) ..........
Nonsmoker Survey (Wave C) ..........
Nonsmoker Survey (Wave D) ..........
Nonsmoker Survey (Wave E) ..........

4,000
4,000
4,000
4,000
2,500
2,000
2,000
2,000
2,000

1
1
1
1
1
1
1
1
1

30/60
30/60
30/60
30/60
30/60
30/60
30/60
30/60
30/60

2,000
2,000
2,000
2,000
1,250
1,000
1,000
1,000
1,000

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

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

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

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

18,584

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

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. 2016–31968 Filed 1–4–17; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–17–0706; Docket No. CDC–2016–
0128]

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 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 National Program of Cancer
Registries Program Evaluation
Instrument.

SUMMARY:

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Number of
responses per
respondent

Number of
respondents

Type of respondent

Written comments must be
received on or before March 6, 2017.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2016–
0128 by any of the following methods:
DATES:

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• 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.
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 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: 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

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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
National Program of Cancer Registries
Program Evaluation Instrument (NPCR–
PEI), (OMB Control Number 0920–0706,

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Federal Register / Vol. 82, No. 3 / Thursday, January 5, 2017 / Notices

expired 05/31/2016)—Reinstatement
with Change—National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
CDC is responsible for administering
and monitoring the National Program of
Cancer Registries (NPCR). The NPCR
provides technical assistance and
funding and sets program standards to
assure that complete local, state,
regional, and national cancer incidence
data are available for national and state
cancer control and prevention activities
and health planning activities.
The Program Evaluation Instrument
has been used for 24 years to monitor
the performance of NPCR grantees in
meeting the required Program
Standards. In 2009, the frequency of the
data collection was reduced from
annual to a biennial schedule in oddnumbered years.
CDC currently supports 48
population-based central cancer
registries (CCR) in 45 states, one
territory, the District of Columbia, and
the Pacific Islands. The National Cancer
Institute supports the operations of
CCRs in the five remaining states.
A new FOA (DP17–1701) will be
released during the first quarter of 2017
and a new project period will begin July
1, 2017. DP17–1701 will allow State
health departments or their Bona Fide
Agents, and U.S. territories that have
not received NPCR funding previously

data content and format, (7) data quality
assurance, (8) data use, (9) collaborative
relationships, (10) advanced activities,
and (11) survey feedback.
Examples of information that can be
obtained from various questions
include, but are not limited to: (1)
Number of filled staff full-time positions
by position responsibility, (2) revision
to cancer reporting legislation, (3)
various data quality control activities,
(4) data collection activities as they
relate to achieving NPCR program
standards for data completeness, and (5)
whether registry data is being used for
comprehensive cancer control programs,
needs assessment/program planning,
clinical studies, or incidence and
mortality estimates.
The NPCR–PEI is needed to receive,
process, evaluate, aggregate, and
disseminate NPCR program information.
The information is used by CDC and the
NPCR-funded registries to monitor
progress toward meeting established
program standards, goals, and
objectives; to evaluate various attributes
of the registries funded by NPCR; and to
respond to data inquiries made by CDC
and other agencies of the federal
government.
CDC intends to seek a three-year
OMB-approval to collect information in
the winter of 2017 and 2019. There are
no costs to respondents except their
time. The estimated annualized burden
hours are summarized in the table
below.

to apply. DP17–1701 NPCR eligibility
will include the 48 awardees funded
under the DP12–1205 FOA and
potentially 6 additional State health
departments or their Bona Fide Agents,
and a combination of U.S. territories as
in DP12–1205.
The NPCR is open to the possibility
of funding the territories individually in
the DP17–1701 FOA. While Pacific
Island Jurisdiction (PIJ) is funded under
one award in DP12–105, they will have
the opportunity to apply as one,
individually, or a combination of
individual and joint applications.
States that were solely funded by
Surveillance, Epidemiology, and End
Result (SEER) in previous years can
easily respond to the questions in the
survey. The information being requested
in the NPCR–PEI are either already
collected by or are readily available to
all CCRs. Thus, the only burden on the
CCRs involves the time it takes to enter
responses on the web-based NPCR–PEI
every other year.
Minor changes to the Program
Evaluation Instrument (NPCR–PEI)
include removing questions determined
to be outdated or inappropriate for this
survey, rewording questions for clarity
and consolidating a few questions. In
addition, questions that showed 100%
compliance in 2015 were deleted.
The NCPR–PEI includes questions
about the following categories of registry
operations: (1) Staffing, (2) legislation,
(3) administration, (4) reporting
completeness, (5) data exchange, (6)

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents

Type of respondents

Form name

NPCR Awardees ...............................

PEI ....................................................

39.5

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.

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

[FR Doc. 2016–31991 Filed 1–4–17; 8:45 am]

[30Day–17–16AWE]

Centers for Disease Control and
Prevention

BILLING CODE 4163–18–P

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Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) has submitted the
following information collection request
to the Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act of 1995. The notice for
the proposed information collection is

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Number of
responses per
respondent
1

Average
burden per
response
(in hrs.)

Total burden
(in hrs.)
2

79

published to obtain comments from the
public and affected agencies.
Written comments and suggestions
from the public and affected agencies
concerning the proposed collection of
information are encouraged. Your
comments should address any of the
following: (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

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