Agency Forms Undergoing Paperwork Reduction Act Review, 31961-31962 [E9-15849]
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31961
Federal Register / Vol. 74, No. 127 / Monday, July 6, 2009 / Notices
respondents, the average annual number
of responses, the time it will take for
each response, and the average annual
burden across 3 years of OMB clearance,
which includes 3 years of data
collection for Cohorts 3 and 4 and two
years of data collection for Cohort 5.
ANNUALIZED AVERAGES: RESPONDENTS, RESPONSES AND HOURS
Number of responses per
respondent
Number of
respondents
Measure name
Hours/
response
Response
burden*
Community Specific Data Collection Activities–Tier I:
GONA Baseline Interviews .......................................................................
GONA Follup Interviews ...........................................................................
GONA Youth Followup Focus Groups .....................................................
Community Plan Focus Groups ...............................................................
Community Plan In-depth Interviews—V.1 ...............................................
Community Plan In-depth Interviews—V.2 ...............................................
Service Provider Focus Groups—V.1 ......................................................
Cross Community Data Collection Activities—Tier II:
Service Provider Focus Groups—V. 2 .....................................................
C-KABS Adult Version ..............................................................................
C-KABS Youth Version ............................................................................
Community Readiness Assessment1 .......................................................
Data Abstraction and Submission Form ...................................................
50
75
150
225
51
51
252
1
1
1
1
1
1
1
0.33
1.0
2.0
2.0
1.0
0.33
2.0
17
75
300
450
51
17
504
126
2,234
2,234
84
156
1
1
1
1
2.0
2.0
0.75
0.75
1.0
6.0
252
1,676
1,676
84
1,872
Total ...................................................................................................
5,688
........................
........................
6,974
* Rounded to the nearest whole number.
Send comments to Summer King,
SAMHSA Reports Clearance Officer,
Room 7–1044, One Choke Cherry Road,
Rockville, MD 20857 and e-mail her a
copy at summer.king@samhsa.hhs.gov.
Written comments should be received
within 60 days of this notice.
Dated: June 26, 2009.
Elaine Parry,
Director, Office of Program Services.
[FR Doc. E9–15915 Filed 7–2–09; 8:45 am]
BILLING CODE 4162–20–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30-Day-09–0556]
Agency Forms Undergoing Paperwork
Reduction Act Review
mstockstill on PROD1PC66 with NOTICES
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) 639–5960 or send an email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC or by fax to (202) 395–6974. Written
comments should be received within 30
days of this notice.
Proposed Project
Assisted Reproductive Technology
(ART) Program Reporting System (0920–
0559, exp. 9/30/2009)—Revision—
National Center for Chronic Disease
Prevention and Health Promotion
(NCCDPHP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The ART program reporting system is
used to comply with section 2(a) of
Public Law 102–493 (known as the
Fertility Clinic Success Rate and
Certification Act of 1992 (FCSRCA)), 42
U.S.C. 263a–1(a)). FCSRCA requires
each ART program to annually report to
the Secretary through the CDC: the
pregnancy success rates achieved by
each ART program, the identity of each
embryo laboratory used by the ART
program, and whether the laboratory is
certified or has applied for certification
under the Act. The reporting system
also makes it possible for the CDC to
publish an annual success rate report to
Congress as specified by the FCSRCA.
This Revision request includes minor
wording changes to improve the clarity
of the question concerning preimplantation genetic diagnosis (PGD),
and an increase in the total estimated
burden hours due to an increase in the
estimated number of responses.
Information is collected electronically
through the National ART Surveillance
System (NASS), a Web-based interface,
or by electronic submission of NASScompatible files. The NASS includes
information about all ART cycles
initiated by any of the ART programs
practicing in the United States and its
territories. The system also collects
information about the pregnancy
outcome of each cycle as well as a
number of data items deemed important
to explain variability in success rates
across ART programs and individuals.
Respondents are the 483 ART
programs in the United States.
Approximately 430 programs are
expected to report an average of 321
ART cycles each. The burden estimate
includes the time for collecting,
validating, and reporting the requested
information. Information is collected on
an annual schedule.
There are no costs to the respondents
other than their time. The total
estimated annualized burden hours are
89,720.
Estimated Annualized Burden Hours
Number of
respondents
Respondents
Form name
ART Programs ................................................
NASS ..............................................................
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430
06JYN1
Number of
responses per
respondent
321
Average
burden per
response
(in hours)
39/60
31962
Federal Register / Vol. 74, No. 127 / Monday, July 6, 2009 / Notices
Dated: June 26, 2009.
Maryam Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E9–15849 Filed 7–2–09; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30-Day–09–0040]
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) 639–5960 or send an email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC or by fax to (202) 395–6974. Written
comments should be received within 30
days of this notice.
Proposed Project
NCEH/ATSDR Exposure
Investigations (EI) [OMB NO: 0923–
0040]—Revision—The National Center
for Environmental Health (NCEH),
Centers for Disease Control and
Prevention (CDC) and the Agency for
Toxic Substances and Disease Registry
(ATSDR).
Background and Brief Description
This is a brief summary of a joint
clearance between the NCEH and
ATSDR, (hereafter ATSDR will
represent both ATSDR and NCEH).
ATSDR is mandated pursuant to the
1980 Comprehensive Environmental
Response, Compensation, and Liability
Act (CERCLA) and its 1986
Amendments, the Superfund
Amendments and Reauthorization Act
(SARA) to prevent or mitigate adverse
human health effects and diminished
quality of life resulting from the
exposure to hazardous substances in the
environment. EIs are an approach
developed by ATSDR that employs
targeted biologic (e.g., urine, blood, hair
samples) and environmental (e.g., air,
water, soil, or food) sampling to
determine whether people are or have
been exposed to unusual levels of
pollutants at specific locations (e.g.,
where people live, spend leisure time,
or anywhere they might come into
contact with contaminants under
investigation). After a chemical release
or suspected release into the
environment, ATSDR’s EIs are used by
public health professionals,
environmental risk managers, and other
decision makers to determine if current
conditions warrant intervention
strategies to minimize or eliminate
human exposure. EIs are usually
requested by officials of a state health
agency, county health departments, the
Environmental Protection Agency, the
general public, and ATSDR staff.
ATSDR has been conducting EIs since
1995 throughout the United States and
seeks revision approved of the currently
approval ICR. All of ATSDR’s
biomedical assessments and some of the
environmental investigations involve
participants. Participation is completely
voluntary. To assist in interpreting the
sampling results, a survey questionnaire
appropriate to the specific contaminant
is administered to participants. ATSDR
collects contact information (e.g., name,
address, phone number) to provide the
participant with their individual results.
Name and address information are
broken into nine separate questions
(data fields) for computer entry. General
information, which includes height,
weight, age, race, gender, etc., is also
collected primarily on biomedical
investigations to assist with results
interpretation. General information can
account for approximately 28 questions
per investigation, out of a set of 57
general information questions. Some of
this information is investigationspecific; not all of this data is collected
for every investigation.
Number of
respondents
Respondents
mstockstill on PROD1PC66 with NOTICES
Exposure Investigation Participants ................................................................
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ATSDR also collects information on
other possible confounding sources of
chemical(s) exposure such as medicines
taken, foods eaten, hobbies, jobs, etc. In
addition, ATSDR asks questions on
recreational or occupational activities
that could increase a participant’s
exposure potential. That information
represents an individual’s exposure
history. To cover those broad categories,
ATSDR is seeking approval for the use
of sets of topical questions. Of these, we
use approximately 12–15 questions
about the pertinent environmental
exposures per investigation. This
number can vary depending on the
number of chemicals being investigated,
the route of exposure (e.g., breathing,
eating, touching), and number of other
sources of the chemical(s) (e.g., products
used, jobs).
Data management procedures have
not changed since the previous
approved information collection and the
instrument does not have extensive
revisions. Only minor non-substantive
changes were made to the Library of
Chemical Exposure Questions by
dividing one question into two; to
clarify, specify and better generate the
information needed.
Typically, the number of participants
in an individual EI ranges from 10 to
less than 50. Questionnaires are
generally needed in less than half of the
EIs (approximately 10–15 per year).
The subject matter for the complete
set of topical questions includes the
following:
(1) Media specific which includes: air
(indoor/outdoor); water (water source
and plumbing); soil, and food
(gardening, fish, game, domestic
animals (e.g., chickens).
(2) Other sources such as:
occupations; hobbies; household
chemical uses and house construction
characteristics; lifestyle (e.g., smoking);
medicines and/or health conditions, and
foods.
There are no costs to respondents
other than their time. The total
estimated annual burden hours are 375.
Estimated Annualized Burden Hours
Number of
responses per
respondent
750
E:\FR\FM\06JYN1.SGM
1
06JYN1
Average
burden per
response
(in hours)
30/60
Total burden
(in hours)
375
]]>Agencies
[Federal Register Volume 74, Number 127 (Monday, July 6, 2009)]
[Notices]
[Pages 31961-31962]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-15849]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30-Day-09-0556]
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) 639-5960 or send an e-mail
to omb@cdc.gov. Send written comments to CDC Desk Officer, Office of
Management and Budget, Washington, DC or by fax to (202) 395-6974.
Written comments should be received within 30 days of this notice.
Proposed Project
Assisted Reproductive Technology (ART) Program Reporting System
(0920-0559, exp. 9/30/2009)--Revision--National Center for Chronic
Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
The ART program reporting system is used to comply with section
2(a) of Public Law 102-493 (known as the Fertility Clinic Success Rate
and Certification Act of 1992 (FCSRCA)), 42 U.S.C. 263a-1(a)). FCSRCA
requires each ART program to annually report to the Secretary through
the CDC: the pregnancy success rates achieved by each ART program, the
identity of each embryo laboratory used by the ART program, and whether
the laboratory is certified or has applied for certification under the
Act. The reporting system also makes it possible for the CDC to publish
an annual success rate report to Congress as specified by the FCSRCA.
This Revision request includes minor wording changes to improve the
clarity of the question concerning pre-implantation genetic diagnosis
(PGD), and an increase in the total estimated burden hours due to an
increase in the estimated number of responses.
Information is collected electronically through the National ART
Surveillance System (NASS), a Web-based interface, or by electronic
submission of NASS-compatible files. The NASS includes information
about all ART cycles initiated by any of the ART programs practicing in
the United States and its territories. The system also collects
information about the pregnancy outcome of each cycle as well as a
number of data items deemed important to explain variability in success
rates across ART programs and individuals.
Respondents are the 483 ART programs in the United States.
Approximately 430 programs are expected to report an average of 321 ART
cycles each. The burden estimate includes the time for collecting,
validating, and reporting the requested information. Information is
collected on an annual schedule.
There are no costs to the respondents other than their time. The
total estimated annualized burden hours are 89,720.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per
Respondents Form name respondents responses per response (in
respondent hours)
----------------------------------------------------------------------------------------------------------------
ART Programs.......................... NASS.................... 430 321 39/60
----------------------------------------------------------------------------------------------------------------
[[Page 31962]]
Dated: June 26, 2009.
Maryam Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E9-15849 Filed 7-2-09; 8:45 am]
BILLING CODE 4163-18-P
