33508 Federal Register / Vol. 72, No.
116 / Monday, June 18, 2007 / Notices
Policy for state TANF and Adult
Assistance topics or the Director,
Division of Tribal TANF Management
for tribal TANF and NEW topics.
3. The authority to deem state TANF
plan amendments complete requires
prior consultation with and concurrence
of the Director, Division of State TANF
Policy.
4. The authority to approve/
disapprove under 45 CFR 205.55(d),
state applications to use alternate
sources of information for income and
eligibility (i.e., IEVS), requires prior
consultation with and the concurrence
of the Office of the Deputy Assistant
Secretary for Administration, the
Director, Division of State TANF Policy,
and with the other programs affected by
the request.
5. The authority to approve/
disapprove under 45 CFR 205.56(a)(1),
IEVS targeting plans, requires prior
consultation with and the concurrence
of the Office of the Deputy Assistance
Secretary for Administration and the
Director, Division of State TANF Policy.
6. The authority to issue letters to
state and tribal TANF grantees
acknowledging their success in
achieving work participation rates for a
fiscal year requires the concurrence of
the Director, Division of State TANF
Policy for state TANF grantees or the
Director, Division of Tribal TANF
Management for tribal TANF grantees.
7. The authority to advise and notify
state TANF grantees on their caseload
reduction credit applications requires
prior consultation with the Director,
Division of State TANF policy.
8. The authority to request caseload
and expenditure data from state TANF
grantees relative to establishing a TFAG
requires consultation with and
concurrence of the Director, Division of
Tribal TANF Management.
9. The authority to approve, request
changes, or defer action on ‘‘Letters of
Intent’’ submitted by tribal applicants
who wish to operate TANF programs
requires prior consultation with and
concurrence of the Director, Division of
Tribal TANF Management.
10. The authority to implement TANF
technical assistance plans and proposals
for the expenditure of technical
assistance funds requires approval of
the Associate Director, TANF in
consultation with the Director, Division
of State & Territory Management.
11. The authority to request
additional information and consult with
jlentini on PROD1PC65 with NOTICES
states and tribes on modifications to
TANF corrective compliance plans
requires prior consultation with and
concurrence of the Director, Division of
State TANF Policy for state TANF plans
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or the Director, Division of Tribal TANF
Management for tribal TANF plans.
12. The authority to approve audit
resolutions letters requires prior
consultation with and the concurrence
of the Regional Office Grants Officer and
the Director, Division of State TANF
Policy for state TANF and Adult
Assistance grantees, or the Director,
Division of Tribal TANF Management
for tribal TANF and NEW grantees.
13. This delegation of authority does
not include the authority to make
determinations on state appeals
concerning audit questions or
recommendations by the Department of
Health and Human Services (HHS)
Audit Agency which involve ACF
program practices reviewed under titles
I, X, XI, and XVI of the Social Security
Act.
14. The authority to approve Adult
Assistance Plans and amendments
requires prior consultation with and
concurrence of the Director, Division of
State TANF Policy.
15. The authority to approve FFP in
payments for repairs to homes owned by
recipients of Adult Assistance requires
prior consultation with and concurrence
of the Regional Office Grants Officer and
Director, Division of State TANF Policy.
(c) Effective Date
This delegation is effective upon the
date of signature.
(d) Effect on Existing Delegations
As related to the authorities delegated
herein, this delegation of authority
supersedes all previous delegations of
authority to the TANF Regional Program
Managers.
I hereby affirm and ratify any actions
taken by the TANF Regional Office
Program Managers, Office of Family
Assistance, which involved the exercise
of the authorities delegated herein prior
to the effective date of this delegation.
Dated: June 8, 2007.
Katherine Bradley,
Associate Director, TANF.
[FR Doc. E7–11707 Filed 6–15–07; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 2007N–0225]
Anthrax Vaccines—Bridging
Correlates of Protection in Animals to
Immunogenicity in Humans; Public
Workshop
AGENCY: Food and Drug Administration,
HHS.
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ACTION: Notice of public workshop.
The Food and Drug Administration
(FDA) is announcing a public workshop
entitled ‘‘Anthrax Vaccines—Bridging
Correlates of Protection in Animals to
Immunogenicity in Humans.’’ The
purpose of the public workshop is to
discuss possible strategies for bridging
animal efficacy data to human
immunogenicity data for investigational
anthrax vaccines.
Date and Time: The public workshop
will be held on November 8, 2007, from
8:30 a.m. to 5 p.m. and November 9,
2007, from 8:30 a.m. to 1 p.m.
Location: Hilton Washington DC
North/Gaithersburg, 620 Perry Pkwy.,
Gaithersburg, MD, 20877, 1–301–977–
8900.
Contact Person: Pier Minor, National
Institutes of Health/Office of the
Director, 6610 Rockledge Dr., Rm.
5WS6, Mail Stop Code 6604, Bethesda,
MD 20892, 301–451–6809, FAX: 301–
402–0659, e-mail: minorp@mail.nih.gov.
Registration: Mail or fax your
registration information (including
name, title, firm name, address,
telephone, and fax number) to the
contact person by October 19, 2007.
There is no registration fee for the
public workshop. Early registration is
recommended because seating is
limited. There will be no onsite
registration.
If you need special accommodations
due to a disability, please contact
Wenda Minor (see Contact Person) at
least 7 days in advance.
SUPPLEMENTARY INFORMATION: FDA’s
Center for Biologics Evaluation and
Research, in cooperation with the
National Institutes of Health and the
Department of Health and Human
Services’ Office of Biomedical
Advanced Research and Development
Authority (BARDA) within the Office of
the Assistant Secretary for Preparedness
and Response, is holding this public
workshop. The public workshop will
include discussions on: (1) Background
information on the ‘‘Animal Rule’’ (May
31, 2002, 67 FR 37988), immunological
correlates of protection, and the toxin
neutralizing assay that will be used to
assess anthrax vaccine immunogenicity
in animals and humans; (2) animal
protection data for anthrax vaccines
given both pre- and post-exposure; and
(3) human immunogenicity data for
anthrax vaccines. The goal of the public
workshop is to discuss ways to expedite
the development of new anthrax
vaccines by providing additional
information about bridging animal
protection data to human
immunogenicity.
18JNN1
 Federal Register / Vol. 72, No. 116 / Monday, June 18, 2007 / Notices
Transcripts: Transcripts of the public
workshop may be requested in writing
from the Freedom of Information Office
(HFI–35), Food and Drug
Administration, 5600 Fishers Lane, rm.
6–30, Rockville, MD 20857,
approximately 15 working days after the
public workshop at a cost of 10 cents
per page. A transcript of the public
workshop will be available on the
Internet at http://www.fda.gov/cber/
minutes/workshop-min.htm.
Dated: June 11, 2007.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E7–11613 Filed 6–15–07; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 2007N–0217]
Licensure of Apheresis Blood
Products; Public Workshop
AGENCY: Food and Drug Administration,
HHS.
ACTION: Notice of public workshop.
The Food and Drug Administration
(FDA) is announcing a public workshop
entitled: Licensure of Apheresis Blood
Products. The purpose of the public
workshop is to educate industry on the
licensure requirements and license
application procedures for Platelets,
Pheresis; Red Blood Cells; and Plasma
collected by automated blood cell
separator devices.
Date and Time: The public workshop
will be held on August 15, 2007, from
8 a.m. to 5 p.m.
Location: The public workshop will
be held at the Lister Hill Center
Auditorium, Bldg. 38A, National
Institutes of Health, 8800 Rockville
Pike, Bethesda, MD 20894.
Contact Person: Rhonda Dawson,
Center for Biologics Evaluation and
Research(HFM–302), Food and Drug
Administration, 1401 Rockville Pike,
suite 200N, Rockville, MD 20852–1448,
301–827–6129, FAX: 301–827–2843, e-
mail: rhonda.dawson@fda.hhs.gov.
Registration: Mail, fax, or e-mail your
registration information (including
name, title, firm name, address,
telephone and fax numbers) to the
contact person by July 31, 2007. There
is no registration fee for the public
workshop. Early registration is
jlentini on PROD1PC65 with NOTICES
recommended because seating is
limited. Registration on the day of the
public workshop will be provided on a
space available basis beginning at 7:30
a.m.
VerDate Aug<31>2005 18:19 Jun 15, 2007 Jkt 211001
If you need special accommodations
due to a disability, please contact
Rhonda Dawson at least 7 days in
advance.
SUPPLEMENTARY INFORMATION: The
public workshop will feature
presentations by experts from
government and industry. The
workshop will include presentations by
FDA on: (1) Requirements for licensure,
and applicable regulations and
guidances, for Platelets, Pheresis; Red
Blood Cells; and Plasma (intended for
transfusion) collected by apheresis
instruments; (2) the FDA managed
review process; and (3) failure
investigations of apheresis products.
Device manufacturers will present an
overview of their devices and review
validation procedures and quality
control processes. Representatives from
blood establishments will present case
studies of licensing applications. FDA
will lead a question and answer session
with workshop participants.
Comments: All individuals wishing to
submit questions to be addressed at the
public workshop should submit written
or electronic comments by July 31,
2007, to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. Submit
electronic comments to http://
www.fda.gov/dockets/ecomments.
Comments are to be identified with the
docket number found in brackets in the
heading of this document. Received
comments may be seen in the Division
of Dockets Management between 9 a.m.
and 4 p.m., Monday through Friday.
Transcripts: Transcripts of the public
workshop may be requested in writing
from the Freedom of Information Office
(HFI–35), Food and Drug
Administration, 5600 Fishers Lane,
rm.6–30, Rockville, MD 20857,
approximately 15 working days after the
public workshop at a cost of 10 cents
per page. A transcript of the public
workshop will be available on the
Internet at http://www.fda.gov/cber/
minutes/workshop-min.htm.
Dated: June 11, 2007.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E7–11615 Filed 6–15–07; 8:45 am]
BILLING CODE 4160–01–S
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33509
DEPARTMENT OF HOMELAND
SECURITY
Federal Emergency Management
Agency
Agency Information Collection
Activities: Proposed Collection;
Comment Request
AGENCY: Federal Emergency
Management Agency, DHS.
ACTION: Notice and request for
comments.
SUMMARY: The Federal Emergency
Management Agency (FEMA), as part of
its continuing effort to reduce
paperwork and respondent burden,
invites the general public and other
Federal agencies to take this
opportunity to comment on a proposed
revised information collection. In
accordance with the Paperwork
Reduction Act of 1995, this notice seeks
comments concerning FEMA’s National
Emergency Training Center (NETC) to
approve and coordinate the use of the
NETC facility for extracurricular
training activities.
SUPPLEMENTARY INFORMATION: The
National Emergency Training Center
(NETC) is a FEMA facility that houses
the Emergency Management Institute
(EMI) and the National Fire Academy
(NFA). NETC provides training and
educational programs for Federal, State,
and local personnel in hazard
mitigation, emergency response and
preparedness, fire prevention and
control, disaster response, and long-
term disaster recovery. Special groups
sponsored by EMI, NFA or other FEMA
organizations may use NETC facilities to
conduct activities closely related to and
in direct support of their activities. Such
groups include other Federal
departments and agencies, groups
charted by Congress such as the
American Red Cross, State and local
governments, volunteer groups, and
national and international associations
representing State and local
governments.
Collection of Information
Title: Approval and Coordination of
requirements to use NETC for
Extracurricular Training Activities.
Type of Information Collection:
Revision of an existing collection.
OMB Number: 1660–0029.
Form Numbers: FEMA Form 75–10,
Request for Housing Accommodations,
and FEMA Form 75–11, Request for Use
of NETC Facility.
Abstract: Data will be obtained from
special groups that request to use NETC
facilities for extracurricular training
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