Agency Information Collection Activities: Proposed Collection: Comment Request, 20602-20603 [2010-9066]
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20602
Federal Register / Vol. 75, No. 75 / Tuesday, April 20, 2010 / Notices
comprised of State asthma control
program representatives over the course
of two years. In collaboration with these
workgroups, the CDC generated specific
questions (qualitative and quantitative
in nature) intended to collect data on
key features of State asthma control
programs:
environment about what is working in
State asthma programs and to identify
potential areas for improvement. There
are no costs to respondents, other than
their time. The total estimated annual
burden hours are 288.
Partnerships, surveillance,
interventions, and evaluation. States
will be asked to provide answers to
these questions once per year in
conjunction with the end of year
reporting of activities and objectives,
described above. These data will be
used to foster a continuous learning
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondent
Forms
Number of
respondents
Number of
response per
respondent
Burden per
response
(in hours)
State Health Departments ..............................
Interim and end of year reports on activities
and objectives.
36
2
4
Dated: April 14, 2010.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. 2010–9086 Filed 4–19–10; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Proposed Collection:
Comment Request
In compliance with the requirement
for opportunity for public comment on
proposed data collection projects
(section 3506(c)(2)(A) of Title 44, United
States Code, as amended by the
Paperwork Reduction Act of 1995, Pub.
L. 104–13), the Health Resources and
Services Administration (HRSA)
publishes periodic summaries of
proposed projects being developed for
submission to the Office of Management
and Budget (OMB) under the Paperwork
Reduction Act of 1995. To request more
information on the proposed project or
to obtain a copy of the data collection
plans and draft instruments, e-mail
paperwork@hrsa.gov or call the HRSA
Reports Clearance Officer at (301) 443–
1129.
Comments are invited on: (a) The
proposed collection of information for
the proper performance of the functions
of the agency; (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.
Proposed Project: The Stem Cell
Therapeutic Outcomes Database (OMB
No. 0915–0310)—Extension
The Stem Cell Therapeutic and
Research Act of 2005 provides for the
collection and maintenance of human
cord blood stem cells for the treatment
of patients and research. The Health
Resources and Services
Number of
respondents
Reporting
Responses
per
respondent
Administration’s (HRSA) Healthcare
Systems Bureau (HSB) has established
the Stem Cell Therapeutic Outcomes
Database. Operation of this database
necessitates certain recordkeeping and
reporting requirements in order to
perform the functions related to
hematopoietic stem cell transplantation
under contract to HHS. The Act requires
the Secretary to contract for the
establishment and maintenance of
information related to patients who
have received stem cell therapeutic
products and to do so using a
standardized, electronic format. Data is
collected from transplant centers in a
manner similar to the data collection
activities conducted by the Center for
International Blood and Marrow
Transplant Research (CIBMTR) and is
used for ongoing analysis of transplant
outcomes. HRSA uses the information
in order to carry out its statutory
responsibilities. Information is needed
to monitor the clinical status of
transplantation and to provide the
Secretary with an annual report of
transplant center-specific survival data.
The estimate of burden is as follows:
Total
responses
Hours per
response
250
250
250
250
250
250
250
40
40
40
28
22
40
25
8,000
8,000
8,000
5,538
4,308
8,000
4,923
2.25
1
2.25
2.25
2.25
2.25
0.5
Total ..........................................................................
erowe on DSK5CLS3C1PROD with NOTICES
Baseline Patient/Day of Transplant Data ........................
Product Receipt/Analysis/Preparation Data .....................
100-Day Post-Transplant Data ........................................
6-Month Post-Transplant Data .........................................
12-Month Post-Transplant Data .......................................
Annual Post-Transplant Data (year two and beyond) .....
Death Information ............................................................
250
........................
46,769
..........................
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20APN1
Total burden
hours
18,000
8,000
18,000
12,460.5
9,693
18,000
2,461.5
86,615
20603
Federal Register / Vol. 75, No. 75 / Tuesday, April 20, 2010 / Notices
E-mail comments to
paperwork@hrsa.gov or mail the HRSA
Reports Clearance Officer, Room 10–33,
Parklawn Building, 5600 Fishers Lane,
Rockville, MD 20857. Written comments
should be received within 60 days of
this notice.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Dated: April 14, 2010.
Sahira Rafiullah,
Director, Division of Policy and Information
Coordination.
Title: Child Care Development Fund
(CCDF)—Reporting Improper
Payments—Instructions for States.
OMB No.: 0970–0323.
Description: The Improper Payments
Information Act of 2002 requires
Federal agencies to annually report error
rate measures. Section 2 of the Improper
[FR Doc. 2010–9066 Filed 4–19–10; 8:45 am]
BILLING CODE 4165–15–P
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Payments Information Act provides for
estimates and reports of improper
payments by Federal agencies. Subpart
K of 45 CFR part 98 requires preparation
and submission of a report of errors
occurring in the administration of Child
Care Development Fund (CCDF) grant
funds once every three years. The
information collected will be used to
prepare the annual Agency Financial
Report (AFR) and will provide
information necessary to offer technical
assistance to grantees.
Respondents: State grantees, the
District of Columbia, and Puerto Rico.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
OMB #0970–0323 Record Review Worksheet .........................................
OMB #0970–0323 Data Entry Form ..........................................................
OMB #0970–0323 State Improper Authorizations for Payment Report ....
erowe on DSK5CLS3C1PROD with NOTICES
Estimated Total Annual Burden
Hours: 84,205.96.
Additional Information: Copies of the
proposed collection may be obtained by
writing to the Administration for
Children and Families, Office of
Administration, Office of Information
Services, 370 L’Enfant Promenade, SW.,
Washington, DC 20447, Attn: ACF
Reports Clearance Officer. All requests
should be identified by the title of the
information collection. E-mail address:
infocollection@acf.hhs.gov.
OMB Comment: OMB is required to
make a decision concerning the
collection of information between 30
and 60 days after publication of this
document in the Federal Register.
Therefore, a comment is best assured of
having its full effect if OMB receives it
within 30 days of publication. Written
comments and recommendations for the
proposed information collection should
be sent directly to the following: Office
of Management and Budget, Paperwork
Reduction Project, Fax: 202–395–7285,
E-mail:
OIRA_SUBMISSION@OMB.EOP.GOV,
Attn: Desk Officer for the
Administration for Children and
Families.
Dated: April 15, 2010.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2010–9050 Filed 4–19–10; 8:45 am]
BILLING CODE 4184–01–P
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Number of
responses per
respondent
17
17
17
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2010–N–0185]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Tobacco Health
Document Submission
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing an
opportunity for public comment on the
proposed collection of certain
information by the agency. Under the
Paperwork Reduction Act of 1995 (the
PRA), Federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension of an existing collection of
information, and to allow 60 days for
public comment in response to the
notice. This notice solicits comments on
the proposed extension of an existing
collection of information pertaining to
the submission of tobacco health
documents under the Family Smoking
Prevention and Tobacco Control Act
(the Tobacco Control Act).
DATES: Submit written or electronic
comments on the collection of
information by June 21, 2010.
ADDRESSES: Submit electronic
comments on the collection of
information to https://
PO 00000
Frm 00049
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Average burden
hours per
response
276.38
276.38
1
Total burden
hours
15.43
0.18
639
72,497.24
845.72
10,863
www.regulations.gov. Submit written
comments on the collection of
information to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. All
comments should be identified with the
docket number found in brackets in the
heading of this document.
FOR FURTHER INFORMATION CONTACT:
Jonna Capezzuto, Office of Information
Management, Food and Drug
Administration, 1350 Piccard Dr., PI50
Rockville, MD 20850, 301–796–3794,
Email:
Jonnalynn.Capezzuto@fda.hhs.gov.
Under the
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.
‘‘Collection of information’’ is defined in
44 U.S.C. 3502(3) and 5 CFR 1320.3(c)
and includes agency requests or
requirements that members of the public
submit reports, keep records, or provide
information to a third party. Section
3506(c)(2)(A) of the PRA (44 U.S.C.
3506(c)(2)(A)) requires Federal agencies
to provide a 60–day notice in the
Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information,
before submitting the collection to OMB
for approval. To comply with this
requirement, FDA is publishing notice
of the proposed collection of
information set forth in this document.
SUPPLEMENTARY INFORMATION:
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]]>Agencies
[Federal Register Volume 75, Number 75 (Tuesday, April 20, 2010)]
[Notices]
[Pages 20602-20603]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-9066]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Proposed Collection:
Comment Request
In compliance with the requirement for opportunity for public
comment on proposed data collection projects (section 3506(c)(2)(A) of
Title 44, United States Code, as amended by the Paperwork Reduction Act
of 1995, Pub. L. 104-13), the Health Resources and Services
Administration (HRSA) publishes periodic summaries of proposed projects
being developed for submission to the Office of Management and Budget
(OMB) under the Paperwork Reduction Act of 1995. To request more
information on the proposed project or to obtain a copy of the data
collection plans and draft instruments, e-mail paperwork@hrsa.gov or
call the HRSA Reports Clearance Officer at (301) 443-1129.
Comments are invited on: (a) The proposed collection of information
for the proper performance of the functions of the agency; (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.
Proposed Project: The Stem Cell Therapeutic Outcomes Database (OMB No.
0915-0310)--Extension
The Stem Cell Therapeutic and Research Act of 2005 provides for the
collection and maintenance of human cord blood stem cells for the
treatment of patients and research. The Health Resources and Services
Administration's (HRSA) Healthcare Systems Bureau (HSB) has established
the Stem Cell Therapeutic Outcomes Database. Operation of this database
necessitates certain recordkeeping and reporting requirements in order
to perform the functions related to hematopoietic stem cell
transplantation under contract to HHS. The Act requires the Secretary
to contract for the establishment and maintenance of information
related to patients who have received stem cell therapeutic products
and to do so using a standardized, electronic format. Data is collected
from transplant centers in a manner similar to the data collection
activities conducted by the Center for International Blood and Marrow
Transplant Research (CIBMTR) and is used for ongoing analysis of
transplant outcomes. HRSA uses the information in order to carry out
its statutory responsibilities. Information is needed to monitor the
clinical status of transplantation and to provide the Secretary with an
annual report of transplant center-specific survival data.
The estimate of burden is as follows:
----------------------------------------------------------------------------------------------------------------
Number of Responses per Total Hours per Total burden
Reporting respondents respondent responses response hours
----------------------------------------------------------------------------------------------------------------
Baseline Patient/Day of 250 40 8,000 2.25 18,000
Transplant Data...............
Product Receipt/Analysis/ 250 40 8,000 1 8,000
Preparation Data..............
100-Day Post-Transplant Data... 250 40 8,000 2.25 18,000
6-Month Post-Transplant Data... 250 28 5,538 2.25 12,460.5
12-Month Post-Transplant Data.. 250 22 4,308 2.25 9,693
Annual Post-Transplant Data 250 40 8,000 2.25 18,000
(year two and beyond).........
Death Information.............. 250 25 4,923 0.5 2,461.5
--------------------------------------------------------------------------------
Total...................... 250 .............. 46,769 .............. 86,615
----------------------------------------------------------------------------------------------------------------
[[Page 20603]]
E-mail comments to paperwork@hrsa.gov or mail the HRSA Reports
Clearance Officer, Room 10-33, Parklawn Building, 5600 Fishers Lane,
Rockville, MD 20857. Written comments should be received within 60 days
of this notice.
Dated: April 14, 2010.
Sahira Rafiullah,
Director, Division of Policy and Information Coordination.
[FR Doc. 2010-9066 Filed 4-19-10; 8:45 am]
BILLING CODE 4165-15-P
