Submission for OMB Review; Comment Request, 35693-35694 [E8-14046]
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35693
Federal Register / Vol. 73, No. 122 / Tuesday, June 24, 2008 / Notices
EXHIBIT 1.—ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Form name
Number of
responses per
respondent
Hours per
response
Total burden
hours
Training participant questionnaire ...................................................................
Organizational leader questionnaire ................................................................
300
75
1
1
30/60
15/60
150
19
Total ..........................................................................................................
375
NA
NA
169
Total burden
hours
Average
hourly wage
rate *
Exhibit 2 shows the estimated
annualized cost burden based on the
respondents’ time to participate in the
study. The total cost burden is estimated
to be $5,552.80.
EXHIBIT 2.—ESTIMATED ANNUALIZED COST BURDEN
Number of
respondents
Form name
Total cost
burden
Training participant questionnaire ......................................................................
Organizational leader questionnaire ..................................................................
300
75
150
19
$32.18 .........
$38.20 .........
$4,827.00
725.80
Total ............................................................................................................
375
169
NA ...............
5,552.80
* Based upon the mean of the average wages for health professionals for the training participant questionnaire and for executives, administrators, and managers for the organizational leader questionnaire presented in the National Compensation Survey: Occupational Wages in the
United States, June 2005, U.S. Department of Labor, Bureau of Labor Statistics.
Estimated Annual Costs to the Federal
Government
The total cost to the government for
this activity is estimated to be $127,442
to conduct the two one-time
questionnaires and to analyze and
present its results. This amount
includes costs for developing the data
collection tools ($50,976); collecting the
data ($25,488); analyzing the data and
reporting the findings ($44,605); and
administrative support activities
($6,373).
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Request for Comments
In accordance with the above-cited
Paperwork Reduction Act legislation,
comments on AHRQ’s information
collection are requested with regard to
any of the following: (a) Whether the
proposed collection of information is
necessary for the proper performance of
AHRQ health care research, quality
improvement and information
dissemination functions, including
whether the information will have
practical utility; (b) the accuracy of
AHRQ’s estimate of burden (including
hours and costs) of the proposed
collection(s) 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 upon the
respondents, including the use of
automated collection techniques or
other forms of information technology.
Comments submitted in response to
this notice will be summarized and
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12:39 Jun 23, 2008
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included in the Agency’s subsequent
request for OMB approval of the
proposed information collection. All
comments will become a matter of
public record.
Dated: June 16, 2006.
Carolyn Clancy,
Director.
[FR Doc. E8–14052 Filed 6–23–08; 8:45 am]
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the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
management activities, for both CDC
and the Agency for Toxic Substances
and Disease Registry.
Diane Allen,
Acting Director, Management Analysis and
Services Office, Centers for Disease Control
and Prevention.
[FR Doc. E8–14136 Filed 6–23–08; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention; Disease, Disability, and
Injury Prevention and Control Special
Emphasis Panel: Postpartum
Hemorrhage Among Women With an
Undiagnosed Bleeding Disorder,
Potential Extramural Project 2008–R–
28
Correction: This notice was published
in the Federal Register on April 18,
2008, Volume 73, Number 76, page
21138. The aforementioned meeting has
been rescheduled to the following:
Time and Date: 1 p.m.–3 p.m., July 8,
2008 (Closed).
For More Information Contact: Linda
Shelton, Program Specialist,
Coordinating Center for Health and
Information Service, Office of the
Director, CDC, 1600 Clifton Road, NE.,
Mailstop E21, Atlanta, GA 30333.
Telephone (404) 498–1194.
The Director, Management Analysis
and Services Office, has been delegated
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
[OMB No.: 0970–0278]
Submission for OMB Review;
Comment Request
Title: Reunification Procedures for
Unaccompanied Alien Children.
Description: Description: Following
the passage of the 2002 Homeland
Security Act (Pub. L. 107–2 96), the
Administration for Children and
Families (ACF), Office of Refugee
Resettlement (ORR), is charged with the
care and placement of unaccompanied
alien children in Federal custody, and
implementing a policy for the release of
these children, when appropriate, upon
the request of suitable sponsors while
awaiting immigration proceedings. In
order for ORR to make determinations
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35694
Federal Register / Vol. 73, No. 122 / Tuesday, June 24, 2008 / Notices
regarding the release of these children,
the potential sponsors must meet certain
conditions pursuant to section 462 of
the Homeland Security Act and the
Flores v. Reno Settlement Agreement
No. CV85 4544–RJK (C.D. Cal. 1997).
The proposed information collection
requests information to be utilized by
ORR for determining the suitability of a
sponsor/respondent for the release of a
minor from ORR custody. The proposed
instruments are the Sponsors Agreement
to Conditions of Release, Verification of
Release, Family Reunification Packet,
Number of
respondents
Instrument
Agreement .....................................................................................................
Verification of Release ...................................................................................
Family Reunification ......................................................................................
Authorization ..................................................................................................
Estimated Total Annual Burden
Hours:
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–
395–6974, Attn: Desk Officer for the
Administration for Children and
Families.
Dated: June 16, 2008.
Robert Sargis,
Reports Clearance, Officer.
[FR Doc. E8–14046 Filed 6–23–08; 8:45 am]
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4,288
4,288
4,288
4,288
Food and Drug Administration
[Docket No. FDA–2008–N–0345]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Current Good
Manufacturing Practices and Related
Regulations for Blood and Blood
Components; and Requirements for
Donor Testing, Donor Notification, and
‘‘Lookback’’
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 information collection requirements
relating to FDA’s regulation of current
good manufacturing practice and related
regulations for blood and blood
components; and requirements for
donor testing, donor notification, and
‘‘lookback.’’
DATES: Submit written or electronic
comments on the collection of
information by August 25, 2008.
ADDRESSES: Submit electronic
comments on the collection of
information to: https://
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.
PO 00000
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Annual Burden Estimates
Number of
responses per
respondent
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
AGENCY:
and the Authorization for Release of
Information.
Respondents: Sponsors requesting
release of unaccompanied alien children
to their custody.
Respondents:
2
1
18
15
Average
burden hours
per response
Total burden
hours
.0835
.167
.0416
0.0222
716
716
3,122
1,428
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 the Chief
Information Officer (HFA–250), Food
and Drug Administration, 5600 Fishers
Lane, Rockville, MD 20857, 301–827–
4659.
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.
With respect to the following
collection of information, FDA invites
comments on these topics: (1) Whether
the proposed collection of information
is necessary for the proper performance
of FDA’s functions, including whether
the information will have practical
utility; (2) the accuracy of FDA’s
estimate of the burden of the proposed
collection of information, including the
validity of the methodology and
assumptions used; (3) ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4)
ways to minimize the burden of the
collection of information on
SUPPLEMENTARY INFORMATION:
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]]>Agencies
[Federal Register Volume 73, Number 122 (Tuesday, June 24, 2008)]
[Notices]
[Pages 35693-35694]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-14046]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
[OMB No.: 0970-0278]
Submission for OMB Review; Comment Request
Title: Reunification Procedures for Unaccompanied Alien Children.
Description: Description: Following the passage of the 2002
Homeland Security Act (Pub. L. 107-2 96), the Administration for
Children and Families (ACF), Office of Refugee Resettlement (ORR), is
charged with the care and placement of unaccompanied alien children in
Federal custody, and implementing a policy for the release of these
children, when appropriate, upon the request of suitable sponsors while
awaiting immigration proceedings. In order for ORR to make
determinations
[[Page 35694]]
regarding the release of these children, the potential sponsors must
meet certain conditions pursuant to section 462 of the Homeland
Security Act and the Flores v. Reno Settlement Agreement No. CV85 4544-
RJK (C.D. Cal. 1997). The proposed information collection requests
information to be utilized by ORR for determining the suitability of a
sponsor/respondent for the release of a minor from ORR custody. The
proposed instruments are the Sponsors Agreement to Conditions of
Release, Verification of Release, Family Reunification Packet, and the
Authorization for Release of Information.
Respondents: Sponsors requesting release of unaccompanied alien
children to their custody.
Respondents:
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average
Instrument Number of responses per burden hours Total burden
respondents respondent per response hours
----------------------------------------------------------------------------------------------------------------
Agreement....................................... 4,288 2 .0835 716
Verification of Release......................... 4,288 1 .167 716
Family Reunification............................ 4,288 18 .0416 3,122
Authorization................................... 4,288 15 0.0222 1,428
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours:
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:
202-395-6974, Attn: Desk Officer for the Administration for Children
and Families.
Dated: June 16, 2008.
Robert Sargis,
Reports Clearance, Officer.
[FR Doc. E8-14046 Filed 6-23-08; 8:45 am]
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