Att B - 60 day FRN

Attachment B_60-Day Federal Register Notice.pdf

National Birth Defects Prevention Study

Att B - 60 day FRN

OMB: 0920-0010

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10750

Federal Register / Vol. 77, No. 36 / Thursday, February 23, 2012 / Notices

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.
The Monthly Vital Statistics Report
forms provide counts of monthly
occurrences of births, deaths, infant
deaths, marriages, and divorces. 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. The

respondents are the registration officials
in the 50 States, the District of
Columbia, New York City, Puerto Rico,
Virgin Islands, Guam, American Samoa,
and the Commonwealth of the Northern
Mariana Islands. In addition, 33 local
(county) officials in New Mexico who
record marriages occurring and divorces
and annulments granted in each county
of New Mexico will use this form. This
form, which takes about 10 minutes to
complete, is designed to collect counts
of monthly occurrences of births,
deaths, infant deaths, marriages, and
divorces immediately following the
month of occurrence.
The Annual Vital Statistics
Occurrence Report Form collects final
annual counts of marriages and divorces
by month for the United States and for
each State. The statistical counts
requested on this form differ from
provisional estimates obtained on the
Monthly Vital Statistics Report Form in

that they represent complete counts of
marriages, divorces, and annulments
occurring during the months of the prior
year. 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. The 58
Respondents for the Annual Vital
Statistics Occurrence Report Form,
which takes about 30 minutes to
complete, are registration officials in
each State and Territory, the District of
Columbia, and New York City.
There are no costs to respondents
other than their time to participate; the
data are routinely available in each
reporting office as a by-product of
ongoing activities. The total estimated
annualized burden hours are 211.

TABLE 1—ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondents

Average
burden per
response
(in hours)

Form name

State, Territory and New Mexico County officials.
State, Territory and Other officials ..................

Monthly Vital Statistics Report .......................

91

12

10/60

Annual Vital Statistics Occurrence Report .....

58

1

30/60

Kimberly S. Lane,
Reports Clearance Officer, Centers for Disease
Control and Prevention.
[FR Doc. 2012–4173 Filed 2–22–12; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60 Day-12–0010]

Proposed Data Collections Submitted
for Public Comment and
Recommendations

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Number of
respondent

Type of respondents

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 Lane, CDC
Reports Clearance Officer, 1600 Clifton

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Road, MS–D74, Atlanta, GA 30333 or
send an email to omb@cdc.gov.
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
The National Birth Defects Prevention
Study (NBDPS), (OMB 0920–0010)—
Reinstatement Without Change—
National Center on Birth Defects and
Developmental Disabilities (NCBDDD),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
CDC has been monitoring the
occurrence of serious birth defects and

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genetic diseases in Atlanta since 1967
through the Metropolitan Atlanta
Congenital Defects Program (MACDP).
The MACDP is a population-based
surveillance system for birth defects in
the 5 counties of Metropolitan Atlanta.
Its primary purpose is to describe the
spatial and temporal patterns of birth
defects occurrence and serves as an
early warning system for new
Teratogens.
The National Birth Defects Prevention
Study (NBDPS) formerly the Birth
Defects Risk Factor Surveillance Study
(BDRFS) began in 1997. The NBDPS is
a case-control study of major birth
defects that includes cases identified
from existing birth defect surveillance
registries in nine states, including
metropolitan Atlanta. NBDPS control
infants are randomly selected from birth
certificates or birth hospital records.
Mothers of case and control infants are
interviewed using a computer-assisted
telephone interview. The interview
takes approximately one hour to
complete. A maximum of four hundred
interviews are planned per year per
center, 300 cases and 100 controls
resulting in a maximum interview
burden of 400 hours for each of the
centers each year.

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10751

Federal Register / Vol. 77, No. 36 / Thursday, February 23, 2012 / Notices
Parents are also asked to collect cheek
cells from themselves and their infant
for DNA. The collection of cheek cells
by the mother, father, and infant takes
about 10 minutes per person. Each
person rubs 1 brush inside the left cheek
and 1 brush inside the right cheek for
a total of 2 brushes per person.
Collection of the cheek cells takes
approximately 1–2 minutes, but the
estimate of burden is 10 minutes to

environmental factors as well as geneenvironment interactions for a broad
range of carefully classified birth
defects.
This request is submitted to obtain
OMB clearance for three additional
years.
There are no costs to the respondents
other than their time.

account for reading and understanding
the consent form and specimen
collection instructions and mailing back
the completed kits. The anticipated
maximum burden for collection of the
cheek cells is 200 hours per center per
year.
Information gathered from both the
interviews and the DNA specimens have
been and will continue to be used to
study independent genetic and

ESTIMATED ANNUALIZED BURDEN HOURS PER CENTER
Number of
respondents

Respondents

Number of
responses per
respondent

Average
burden per response

Total burden
hours

NBDPS case/control interview .........................................................................
Biologic Specimen Collection ..........................................................................

400
1,200

1
1

1
10/60

400
200

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

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

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

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

600

Kimberly S. Lane,
Acting Reports Clearance Officer.
[FR Doc. 2012–4170 Filed 2–22–12; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Proposed Projects: Data Collection for
some of the Children’s Bureau Funded
Discretionary Programs.

Title: Performance Measurement OnLine Tool (PMOTOOL).
OMB No.: New Collection.
Description: The Performance
Measurement On-Line Tool
(PMOTOOL) was designed by the
Children’s Bureau to collect data, in an
automated format, from specified
discretionary grants funded by the
Children’s Bureau. The data collected
by this instrument will be submitted by
individual discretionary grantees
funded under the following programs:
Abandoned Infants Assistance Program,
Infant Adoption Awareness Program,
Adoption Opportunities Program, Child
Abuse and Neglect Program and the
Child Welfare Training Program.

Grantees will submit this information
on a semi-annual basis in conjunction
with their semi-annual program
progress report.
The purpose of this data collection is
to assist the Children’s Bureau in using
the aggregated data to examine the
social impact or public benefit under
each funded federal program. These
measurable outcomes will serve as
evidence that the federally funded
programs are making progress toward
achieving broad, legislated program
goals.
Respondents: Selected clusters of
competitive grant programs funded by
the Children’s Bureau.

ANNUAL BURDEN ESTIMATES
Instrument

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Performance Measurement
On-Line Tool.
Performance Measurement
On-Line Tool.
Performance Measurement
On-Line Tool.
Performance Measurement
On-Line Tool.
Performance Measurement
On-Line Tool.

Number of respondents

Number of responses per
respondent

Average burden hours per
response

Total burden
hours

Abandoned Infants Assistance
Program Range 20–30.
Infant Adoption Awareness
Program Range 6.
Adoption Opportunities Program Range 45–55.
Child Abuse and Neglect Program Range 30–40.
Child Welfare Training Program Range 40–50.

2 per fiscal year ......................

One hour per response field ..

Range 40–60

2 per fiscal year ......................

One hour per response field ..

Range 12

2 per fiscal year ......................

One hour per response field ..

2 per fiscal year ......................

One hour per response field ..

Range 90–
110
Range 60–80

2 per fiscal year ......................

One hour per response field ..

Estimated Total Annual Burden
Hours: 282–350.
In compliance with the requirements
of Section 506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the
Administration for Children and
Families is soliciting public comment
on the specific aspects of the
information collection described above.
Copies of the proposed collection of
information can be obtained and

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comments may be forwarded by writing
to the Administration for Children and
Families, Office of Planning, Research
and Evaluation, 370 L’Enfant
Promenade SW., Washington, DC 20447,
Attn: ACF Reports Clearance Officer.
Email address:
infocollection@acf.hhs.gov. All requests
should be identified by the title of the
information collection.

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Range 80–
100

The Department specifically requests
comments 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)
the quality, utility, and clarity of the
information to be collected; and (d)

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