Att 2 - 60 day FRN

Federal Register / Vol. 77, No. 214 / Monday, November 5, 2012 / Notices
3090–0246, Packing List Clause, by any
of the following methods:
• Regulations.gov: http://
www.regulations.gov. Submit comments
via the Federal eRulemaking portal by
searching the OMB control number.
Select the link ‘‘Submit a Comment’’
that corresponds with ‘‘Information
Collection 3090–0246, Packing List
Clause’’. Follow the instructions
provided at the ‘‘Submit a Comment’’
screen. Please include your name,
company name (if any), and
‘‘Information Collection 3090–0246,
Packing List Clause’’ on your attached
document.
• Fax: 202–501–4067.
• Mail: General Services
Administration, Regulatory Secretariat
(MVCB), 1275 First Street NE.,
Washington, DC 20417. ATTN: Hada
Flowers/IC 3090–0246, Packing List
Clause.
Instructions: Please submit comments
only and cite Information Collection
3090–0246, Packing List Clause, in all
correspondence related to this
collection. All comments received will
be posted without change to http://
www.regulations.gov, including any
personal and/or business confidential
information provided.
FOR FURTHER INFORMATION CONTACT:

Deborah Eble, Procurement Analyst,
GSA Policy Integrity Workforce, by
telephone (215) 446–5823 or via email
at [email protected].
SUPPLEMENTARY INFORMATION:

A. Purpose
GSAR clause 552.211–77, Packing
List, requires a contractor to include a
packing list that verifies placement of an
order and identifies the items shipped.
In addition to information contractors
would normally include on packing
lists, the identification of cardholder
name, telephone number and the term
‘‘Credit Card’’ is required.

WREIER-AVILES on DSK5TPTVN1PROD with NOTICES

B. Annual Reporting Burden
Respondents: 4,000.
Responses per Respondent: 233.
Hours per Response: .00833.
Total Burden Hours: 7,757.
Obtaining Copies of Proposals:
Requesters may obtain a copy of the
information collection documents from
the General Services Administration,
Regulatory Secretariat (MVCB), 1275
First Street NE., Washington, DC 20417,
telephone (202) 501–4755. Please cite
OMB Control No. 3090–0246, Packing
List Clause, in all correspondence.

VerDate Mar<15>2010

15:30 Nov 02, 2012

Jkt 229001

Dated: October 10, 2012.
Joseph A. Neurauter,
Director, Office of Acquisition Policy & Senior
Procurement Executive (MV).
[FR Doc. 2012–26955 Filed 11–2–12; 8:45 am]
BILLING CODE 6820–61–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–13–0706]

Proposed Data Collections Submitted
for Public Comment and
Recommendations
In compliance with the requirement
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for
opportunity for public comment on
proposed data collection projects, the
Centers for Disease Control and
Prevention (CDC) will publish periodic
summaries of proposed projects. To
request more information on the
proposed projects or to obtain a copy of
the data collection plans and
instruments, call 404–639–7570 and
send comments to Kimberly S. Lane,
1600 Clifton Road, MS–D74, Atlanta,
GA 30333 or send an email to
[email protected].
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; and (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. Written comments should
be received within 60 days of this
notice.
Proposed Project
National Program of Cancer Registries
Program Evaluation Instrument (NPCR–
PEI) (OMB No. 0920–0706, exp. 12/31/
2011)—Reinstatement—National Center
for Chronic Disease Prevention and
Health Promotion (NCCDPHP), Centers
for Disease Control and Prevention
(CDC).
Background and Brief Description
The National Program of Cancer
Registries (NPCR), administered by the
Centers for Disease Control and
Prevention (CDC), was established to

PO 00000

Frm 00036

Fmt 4703

Sfmt 4703

66467

provide funding for states and territories
to: (1) Improve existing state-based
cancer registries; (2) plan and
implement registries where none
existed; (3) develop model legislation
and regulations for states to enhance the
viability of registry operations; (4) set
standards for data completeness,
timeliness, and quality; (5) provide
training for registry personnel; and (6)
help establish a computerized reporting
and data-processing system. Through
the NPCR, 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 CCR
in the five remaining states.
Through the NPCR, CDC provides
technical assistance and funding and
sets program standards to assure that
complete cancer incidence data are
available for national and state cancer
control and prevention activities and
other health planning activities. NPCRfunded CCR are the primary source of
cancer surveillance data for United
States Cancer Statistics (USCS), which
CDC has published annually since 2002.
Over a 17-year period, CDC has
collected information from NPCR
grantees to monitor their performance in
meeting the required Program Standards
(NPCR Program Evaluation Instrument,
OMB No. 0920–0706, exp. 12/31/2011).
The NPCR Program Evaluation
Instrument (PEI) is a secure, web-based
method of collecting information about
registry operations, including: Staffing,
legislation, administration, reporting
completeness, data exchange, data
content and format, data quality
assurance, data use, collaborative
relationships, advanced activities, and
survey feedback. Examples of
information that can be obtained from
various questions include, but are not
limited to: (1) The number of filled fulltime staff positions by position
responsibility, (2) data quality control
activities, (3) data collection activities as
they relate to achieving NPCR standards
for data completeness, (4) electronic
reporting, (5) linkage with other
databases and (6) whether registry data
are used for comprehensive cancer
control program planning and
evaluation.
The most recent PEI reports were
submitted to CDC in 2011. Since 2009,
data collection had been conducted on
a biennial schedule in odd-numbered
years. In late 2011, CDC discontinued
the NPCR PEI clearance in preparation
for a review of program standards. At
this time, CDC seeks OMB approval to
reinstate the NPCR PEI clearance. Minor
changes to the PEI will be implemented

E:\FR\FM\05NON1.SGM

05NON1

66468

Federal Register / Vol. 77, No. 214 / Monday, November 5, 2012 / Notices

based on the revised NPCR standards.
Additional changes include a reduction
in the estimated number of NPCR
grantees and an increase in the
estimated burden per response.
Information will continue to be
collected electronically in oddnumbered years. OMB approval is
requested for three years to support data
collection in 2013 and 2015. The total

NPCR-funded registries will use the data
to monitor progress toward meeting
objectives and established program
standards; to describe various attributes
of the NPCR-funded registries; and to
respond to inquiries about the program.
There are no costs to respondents
except their time. The estimated
annualized burden hours are
summarized in the table below.

number of NPCR grantees is 48. For two
cycles of data collection over a threeyear period, the annualized number of
grantees is 32 (48+48/3=32). The
estimated burden per response is 2
hours.
The NPCR–PEI data collection is
needed to receive, process, evaluate,
aggregate, and disseminate NPCR
program information. CDC and the

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

Number of
responses per
respondent

Total burden
(in hrs.)

Form name

NPCR Grantees ................................

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

32

1

2

64

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

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

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

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

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

64

Dated: October 30, 2012.
Ron A. Otten,
Director, Office of Scientific Integrity (OSI),
Office of the Associate Director for Science
(OADS), Office of the Director, Centers for
Disease Control and Prevention.

Background and Brief Description

[FR Doc. 2012–26899 Filed 11–2–12; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–13–12RI]

Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under
review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
requests, call the CDC Reports Clearance
Officer at (404) 639–7570 or send an
email to [email protected]. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC 20503 or by fax to (202) 395–5806.
Written comments should be received
within 30 days of this notice.
WREIER-AVILES on DSK5TPTVN1PROD with NOTICES

Number of
respondents

Type of respondents

Proposed Project
Information Collection on foreignborn, migrant, refugee and other mobile
populations with current or future ties
to the United States—New—National
Center for Emerging and Zoonotic
Infectious Diseases (NCEZID), Division
of Global Migration and Quarantine
(DGMQ), Centers for Disease Control
and Prevention (CDC).

VerDate Mar<15>2010

15:30 Nov 02, 2012

Jkt 229001

The Centers for Disease Control and
Prevention (CDC), National Center for
Emerging and Zoonotic Infectious
Diseases (NCEZID), Division of Global
Migration and Quarantine (DGMQ),
requests approval of a new ‘‘generic
clearance’’ to better understand the
health status, risk factors for disease and
other health outcomes among foreignborn, migrant, refugee and other mobile
populations with current or future ties
to the United States. Insights gained
from information collections will assist
in the planning, implementation and
improvement of disease prevention and
control activities.
The information collection for which
approval is sought is in accordance with
DGMQ’s mission to reduce morbidity
and mortality among immigrants,
refugees, travelers, expatriates, and
other globally mobile populations, and
to prevent the introduction,
transmission, or spread of
communicable diseases from foreign
countries into the United States. This
mission is supported by delegated legal
authorities.
Section 361 of the Public Health
Service (PHS) Act (42 U.S.C. 264)
authorizes the Secretary of Health and
Human Services (HHS) to make and
enforce regulations necessary to prevent
the introduction, transmission, or
spread of communicable diseases from
foreign countries or possessions into the
United States and from one state or
possession into any other state or
possession. These regulations are
codified in 42 Code of Federal
Regulations (CFR) Parts 70 and 71.
The Secretary of Health and Human
Services also has the legal authority to
establish regulations outlining the
requirements for the medical

PO 00000

Frm 00037

Fmt 4703

Sfmt 4703

examination of aliens before they may
be admitted into the United States. This
authority is provided under Section
212(a)(1)(A) of the Immigration and
Nationality Act (8 U.S.C. 1182(a)(1)(A))
and Section 325 of the Public Health
Service Act. These regulations are
codified in 42 CFR Part 34, which
establish requirements that determine
whether aliens can be admitted into the
United States.
Successful implementation of
DGMQ’s regulatory authority and public
health mission requires a variety of
information collections with foreignborn, migrant and other mobile
populations with current or future ties
to the United States. These include but
are not limited to: immigrants,
international travelers, asylees and
refugees, expatriates, border region
residents, temporary migrants, and
permanent alien residents.
The purpose of the new ‘‘generic
clearance’’ is to better understand the
health status, risk factors for disease and
other health outcomes among foreignborn, migrant, refugee and other mobile
populations with current or future ties
to the United States. Numerous types of
information will be collected under the
auspices of this generic OMB clearance.
These include, but are not limited to,
knowledge, attitudes, beliefs, behavioral
intentions, practices, behaviors, skills,
self-efficacy, and health information
needs and sources.
The proposed generic clearance is
needed for DGMQ to fulfill its
regulatory authority and public health
mission, and will allow DGMQ to
quickly collect important health-related
information from the aforementioned
hard-to-reach populations in order to
improve routine and emergency public
health programs and activities. Prior to
each proposed information collection,

E:\FR\FM\05NON1.SGM

05NON1