State Health Fraud Task Force Grants; Availability of Funds; Request for Applications; Correction, 9656-9657 [05-3710]
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9656
Federal Register / Vol. 70, No. 38 / Monday, February 28, 2005 / Notices
helping agencies achieve a smooth and
successful transition to eTS by assisting
you in effectively determining your eTS
strategy, selecting an eTS vendor and
awarding a task order, and executing
your agency-wide migration to eTS.
Working together in a collaborative
partnership, we can ensure timely
success of this very important
Presidential initiative.
Dated: February 17, 2005.
G. Martin Wagner,
Associate Administrator, Office of
Governmentwide Policy.
[FR Doc. 05–3722 Filed 2–25–05; 8:45 am]
BILLING CODE 6820–14–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
[Document Identifier: OS–4040–0002]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Office of the Secretary,
Grants.gov Program Management Office.
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Office of the Secretary (OS), Department
of Health and Human Services, is
publishing the following summary of
proposed collections for public
comment. Interested persons are invited
to send comments regarding this burden
estimate or any other aspect of this
collection of information, including any
of the following subjects: (1) The
necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions;
(2) the accuracy of the estimated
burden; (3) ways to enhance the quality,
utility, and clarity of the information to
be collected; and (4) the use of
automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
1. Type of Information Collection
Request: Regular;
Title of Information Collection: SF–
424 Mandatory (M);
Form/OMB No.: OS–4040–0002.
Use: The SF–424(M) will become the
government-wide data set for
applications, plans, and related
submissions under mandatory grant
programs. Federal agencies and
applicants/recipients under mandatory
grant programs will use the standard
data set and definitions for paper and
electronic applications/plans/related
submissions. At this time, the Federal
AGENCY:
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16:34 Feb 25, 2005
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agencies are proposing a set of data
elements to be used as cover
information. Additional standard data
elements for other components of an
application/plan, e.g., a standard
budget, may be proposed at a later date.
The proposed standard data set will
replace numerous agency data sets and
reduce the administrative burden placed
on the grants community. Federal
agencies will not be required to collect
all of the information included in the
proposed data set. The agency will
identify the data that must be provided
by applicants through instructions that
will accompany the application
package.
Frequency: Recordkeeping,
Application, and on occasion;
Affected Public: Federal, State, local,
or tribal governments, farms, and not for
profit institutions;
Annual Number of Respondents:
1,161;
Total Annual Responses: 21,900;
Average Burden Per Response: 1 hour;
Total Annual Hours: 21,900.
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, access the HHS Web
site address at https://www.hhs.gov/
oirm/infocollect/pending/ or e-mail your
request, including your address, phone
number, OMB number, and OS
document identifier, to
naomi.cook@hhs.gov, or call the Reports
Clearance Office on (202) 690–6162.
Written comments and
recommendations for the proposed
information collections must be mailed
within 60 days of this notice directly to
the OS Paperwork Clearance Officer
designated at the following address:
Department of Health and Human
Services, Office of the Secretary,
Assistant Secretary for Budget,
Technology, and Finance, Office of
Information and Resource Management,
Attention: Naomi Cook (4040–0002),
Room 531–H, 200 Independence
Avenue, SW., Washington DC 20201.
Dated: February 22, 2005.
Robert E. Polson,
Office of the Secretary, Paperwork Reduction
Act Reports Clearance Officer.
[FR Doc. 05–3711 Filed 2–25–05; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
State Health Fraud Task Force Grants;
Availability of Funds; Request for
Applications; Correction
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice; correction.
The Food and Drug Administration
(FDA) is correcting notice document 04–
14593 beginning on page 36091 in the
issue of Monday, June 28, 2004, by
making the following corrections:
On page 36091, in the first column,
the second sentence under SUMMARY is
corrected to read: ‘‘Grant funds will be
used to assist agencies in identifying
and prosecuting perpetrators of health
fraud and AIDS Health Fraud; obtain
and disseminate information on the use
of fraudulent drugs and therapies;
disseminate information on approved
drugs and therapies; and provide health
fraud information obtained by the State
Health Fraud Task Force to State health
agencies, community based
organizations, and FDA staff.’’
On page 36091, in the first column,
the DATES section is corrected to read:
‘‘DATES: The application receipt date for
new applications is April 30, 2005. The
application receipt date for new
applications for each subsequent year
that this program is in effect will be
April 30.’’
On page 36091, in the first column,
the ADDRESSES section is corrected to
read:
‘‘ADDRESSES: FDA is accepting new
applications for this program
electronically via Grants.gov.
Applicants are strongly encouraged to
apply electronically by visiting the Web
site https://www.grants.gov and
following instructions under ‘APPLY.’
The applicant must register in the
Central Contractor Registration (CCR)
database in order to be able to submit
the application. Information about CCR
is available at https://www.grants.gov/
CCRRegister. The applicant must
register with the Credential Provider for
Grants.gov. Information about this
requirement is available at https://
www.grants.gov/CredentialProvider.
If applicants cannot submit
applications through the electronic
process, application forms are available
from, and completed applications
should be submitted to, Djuana Gibson,
Division of Contracts and Grants
Management (HFA–500), Food and Drug
Administration, 5600 Fishers Lane, rm.
2131, Rockville, MD 20857, 301–827–
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28FEN1
Federal Register / Vol. 70, No. 38 / Monday, February 28, 2005 / Notices
7177, e-mail: dgibson@oc.fda.gov.
Application forms PHS 5161–1 are
available via the Internet at: https://
www.hhs.gov/forms (revised 7/00).
Applications hand-carried or
commercially delivered should be
addressed to 5630 Fishers Lane (HFA–
500), rm. 2131, Rockville, MD 20852.
An application not received in time for
orderly processing will be returned to
the applicant without consideration.’’
On page 36091, in the second column,
FOR FURTHER INFORMATION CONTACT is
corrected to read:
‘‘FOR FURTHER INFORMATION CONTACT:
Regarding the administrative and
financial management aspects of
this notice: Djuana Gibson (see
ADDRESSES).
Regarding the programmatic aspects
of this notice: Stephen Toigo,
Division of Federal-State Relations
(DFSR), Office of Regulatory Affairs,
Food and Drug Administration
(HFC–150), 5600 Fishers Lane, rm.
12–07, Rockville, MD 20857, 301–
827–6906, or access the Internet at:
https://www.fda.gov/ora/fed_state/
default.htm. For general ORA
program information contact your
Public Affairs Specialists at https://
www.fda.gov/ora/fed_state/
DFSR_Activities/.’’
On page 36091, in the second column,
under section I, the first paragraph is
corrected to read: ‘‘FDA will support
projects covered by this notice under
title XVII of the Public Health Service
Act (42 U.S.C. 1702). FDA’s project
program is described in the Catalog of
Federal Domestic Assistance, No.
93.245, and applicants are limited to
States that have an existing AIDS Health
Fraud Task Force or States that are in
the process of developing a Health
Fraud Task Force.’’
On page 30692, in the first column,
under section V.A, a sentence is added
at the end of the paragraph that reads:
‘‘A Current Listing of SPOCs can be
found at https://www.whitehouse.gov/
omb/grants/spoc.html.’’
On page 36092, in the third column,
under section VII, the paragraph is
corrected to read: ‘‘Applicants are
encouraged to apply electronically (see
ADDRESSES). If not, the original and two
copies of the completed grant
application Form PHS–5161–1 (revised
7/00) for State and local governments
should be delivered to the Grants
Management Office. The receipt date is
April 30, 2005. No supplemental
material or addenda will be accepted
after the receipt date.’’
On page 36092, in the third column,
under section VIII.A, the section is
corrected to read:
‘‘A. Submission Instructions
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16:34 Feb 25, 2005
Jkt 205001
Applications will be accepted during
working hours, 8 a.m. to 4:30 p.m.,
Monday through Friday, on or before
the established receipt date.
Applications will be considered
received on time if sent or mailed on or
before the receipt date as evidenced by
a legible U.S. Postal Service dated
postmark or a legible date receipt from
a commercial carrier, unless they arrive
too late for orderly processing. Private
metered postmarks shall not be
acceptable as proof of timely mailing.
Applications not received on time will
not be considered for review and will be
returned to the applicant. Applicants
should note that the U.S. Postal Service
does not uniformly provide dated
postmarks. Before relying on this
method, applicants should check with
their local post office.
Do not send applications to the Center
for Scientific Research, NIH. Any
application sent to NIH that is then
forwarded to FDA and not received in
time for orderly processing will be
deemed unresponsive and returned to
the applicant. FDA is able to receive
applications via the Internet.
The outside of the mailing package
and item 2 of the application face page
should be labeled ‘Response to FDA–
ORA–04–2.’ You must submit only one
application, an original and two copies,
per package.’’
Please note that the only change to
section VIII.A is that FDA is now
accepting applications via the Internet.
Dated: February 18, 2005.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. 05–3710 Filed 2–25–05; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
General and Plastic Surgery Devices
Panel of the Medical Devices Advisory
Committee; Notice of Meeting
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
This notice announces a forthcoming
meeting of a public advisory committee
of the Food and Drug Administration
(FDA). The meeting will be open to the
public.
Name of Committee: General and
Plastic Surgery Devices Panel of the
Medical Devices Advisory Committee.
General Function of the Committee:
To provide advice and
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9657
recommendations to the agency on
FDA’s regulatory issues.
Date and Time: The meeting will be
held on April 11, 2005, from 8 a.m. to
5:30 p.m., on April 12, 2005, from 8 a.m.
to 6 p.m., and on April 13, 2005, from
8 a.m. to 6 p.m.
Location: Hilton Washington DC
North/Gaithersburg, Grand Ballroom,
620 Perry Pkwy., Gaithersburg, MD.
Contact Person: David Krause, Center
for Devices and Radiological Health
(HFZ–410), Food and Drug
Administration, 9200 Corporate Blvd.,
Rockville, MD 20850, 301–594–3090,
ext. 141, or FDA Advisory Committee
Information Line, 1–800–741–8138
(301–443–0572 in the Washington, DC
area), code 3014512519. Please call the
Information Line or access the Internet
address of https://www.fda.gov/cdrh/
panelmtg.html for up-to-date
information on this meeting.
Agenda: On April 11, 2005, the
committee will hear oral presentations
from the public. On April 12 and 13,
2005, the committee will discuss, make
recommendations, and vote on two
premarket approval applications for
Silicone Gel-Filled Breast Prostheses.
Background information, including the
agenda and questions for the committee,
will be available to the public on April
8, 2005, on the Internet at https://
www.fda.gov/cdrh/panelmtg.html.
Procedure: Interested persons may
present data, information, or views,
orally or in writing, on issues pending
before the committee. Written
submissions may be made to the contact
person by March 28, 2005. Oral
presentations from the public will be
scheduled on April 11, 2005, between
approximately 8 a.m. and 5:30 p.m., and
on April 12 and 13, 2005, between
approximately 2:45 p.m. and 3:45 p.m.
Time allotted for each presentation is
limited. Those desiring to make formal
oral presentations should notify the
contact person before March 28, 2005,
and submit a brief statement of the
general nature of the comments they
wish to present, and the names and
addresses of proposed participants.
Persons attending FDA’s advisory
committee meetings are advised that the
agency is not responsible for providing
access to electrical outlets.
FDA welcomes the attendance of the
public at its advisory committee
meetings and will make every effort to
accommodate persons with physical
disabilities or special needs. If you
require special accommodations due to
a disability, please contact AnnMarie
Williams, Conference Management
Staff, at 240–276–0450, ext. 113, at least
7 days in advance of the meeting.
E:\FR\FM\28FEN1.SGM
28FEN1
Agencies
[Federal Register Volume 70, Number 38 (Monday, February 28, 2005)]
[Notices]
[Pages 9656-9657]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-3710]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
State Health Fraud Task Force Grants; Availability of Funds;
Request for Applications; Correction
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice; correction.
-----------------------------------------------------------------------
The Food and Drug Administration (FDA) is correcting notice
document 04-14593 beginning on page 36091 in the issue of Monday, June
28, 2004, by making the following corrections:
On page 36091, in the first column, the second sentence under
SUMMARY is corrected to read: ``Grant funds will be used to assist
agencies in identifying and prosecuting perpetrators of health fraud
and AIDS Health Fraud; obtain and disseminate information on the use of
fraudulent drugs and therapies; disseminate information on approved
drugs and therapies; and provide health fraud information obtained by
the State Health Fraud Task Force to State health agencies, community
based organizations, and FDA staff.''
On page 36091, in the first column, the DATES section is corrected
to read:
``DATES: The application receipt date for new applications is April 30,
2005. The application receipt date for new applications for each
subsequent year that this program is in effect will be April 30.''
On page 36091, in the first column, the ADDRESSES section is
corrected to read:
``ADDRESSES: FDA is accepting new applications for this program
electronically via Grants.gov. Applicants are strongly encouraged to
apply electronically by visiting the Web site https://www.grants.gov and
following instructions under `APPLY.' The applicant must register in
the Central Contractor Registration (CCR) database in order to be able
to submit the application. Information about CCR is available at http:/
/www.grants.gov/CCRRegister. The applicant must register with the
Credential Provider for Grants.gov. Information about this requirement
is available at https://www.grants.gov/CredentialProvider.
If applicants cannot submit applications through the electronic
process, application forms are available from, and completed
applications should be submitted to, Djuana Gibson, Division of
Contracts and Grants Management (HFA-500), Food and Drug
Administration, 5600 Fishers Lane, rm. 2131, Rockville, MD 20857, 301-
827-
[[Page 9657]]
7177, e-mail: dgibson@oc.fda.gov. Application forms PHS 5161-1 are
available via the Internet at: https://www.hhs.gov/forms (revised 7/00).
Applications hand-carried or commercially delivered should be addressed
to 5630 Fishers Lane (HFA-500), rm. 2131, Rockville, MD 20852. An
application not received in time for orderly processing will be
returned to the applicant without consideration.''
On page 36091, in the second column, FOR FURTHER INFORMATION
CONTACT is corrected to read:
``FOR FURTHER INFORMATION CONTACT:
Regarding the administrative and financial management aspects of
this notice: Djuana Gibson (see ADDRESSES).
Regarding the programmatic aspects of this notice: Stephen Toigo,
Division of Federal-State Relations (DFSR), Office of Regulatory
Affairs, Food and Drug Administration (HFC-150), 5600 Fishers Lane, rm.
12-07, Rockville, MD 20857, 301-827-6906, or access the Internet at:
https://www.fda.gov/ora/fed_state/default.htm. For general ORA program
information contact your Public Affairs Specialists at https://
www.fda.gov/ora/fed_state/DFSR_Activities/.''
On page 36091, in the second column, under section I, the first
paragraph is corrected to read: ``FDA will support projects covered by
this notice under title XVII of the Public Health Service Act (42
U.S.C. 1702). FDA's project program is described in the Catalog of
Federal Domestic Assistance, No. 93.245, and applicants are limited to
States that have an existing AIDS Health Fraud Task Force or States
that are in the process of developing a Health Fraud Task Force.''
On page 30692, in the first column, under section V.A, a sentence
is added at the end of the paragraph that reads: ``A Current Listing of
SPOCs can be found at https://www.whitehouse.gov/omb/grants/spoc.html.''
On page 36092, in the third column, under section VII, the
paragraph is corrected to read: ``Applicants are encouraged to apply
electronically (see ADDRESSES). If not, the original and two copies of
the completed grant application Form PHS-5161-1 (revised 7/00) for
State and local governments should be delivered to the Grants
Management Office. The receipt date is April 30, 2005. No supplemental
material or addenda will be accepted after the receipt date.''
On page 36092, in the third column, under section VIII.A, the
section is corrected to read:
``A. Submission Instructions
Applications will be accepted during working hours, 8 a.m. to 4:30
p.m., Monday through Friday, on or before the established receipt date.
Applications will be considered received on time if sent or mailed on
or before the receipt date as evidenced by a legible U.S. Postal
Service dated postmark or a legible date receipt from a commercial
carrier, unless they arrive too late for orderly processing. Private
metered postmarks shall not be acceptable as proof of timely mailing.
Applications not received on time will not be considered for review and
will be returned to the applicant. Applicants should note that the U.S.
Postal Service does not uniformly provide dated postmarks. Before
relying on this method, applicants should check with their local post
office.
Do not send applications to the Center for Scientific Research,
NIH. Any application sent to NIH that is then forwarded to FDA and not
received in time for orderly processing will be deemed unresponsive and
returned to the applicant. FDA is able to receive applications via the
Internet.
The outside of the mailing package and item 2 of the application
face page should be labeled `Response to FDA-ORA-04-2.' You must submit
only one application, an original and two copies, per package.''
Please note that the only change to section VIII.A is that FDA is
now accepting applications via the Internet.
Dated: February 18, 2005.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. 05-3710 Filed 2-25-05; 8:45 am]
BILLING CODE 4160-01-S