Agency Forms Undergoing Paperwork Reduction Act Review, 26118-26119 [E8-10215]
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26118
Federal Register / Vol. 73, No. 90 / Thursday, May 8, 2008 / Notices
received no comments on this proposal.
Therefore, the Bureau adopts its
proposal.
71. Finally, the Bureau notes that in
the event of a default, the Commission
may reauction the license or offer it to
the next highest bidder (in descending
order) at its final bid amount. In
addition, if a default or disqualification
involves gross misconduct,
misrepresentation, or bad faith by an
applicant, the Commission may declare
the applicant and its principals
ineligible to bid in future auctions, and
may take any other action that it deems
necessary, including institution of
proceedings to revoke any existing
licenses held by the applicant.
F. Refund of Remaining Upfront
Payment Balance
72. All upfront payments submitted
by applicants in Auction 77 may be
available to be refunded after the
conclusion of the auction; subject to any
required payments (i.e. winning bid,
deficiency, and/or default payments).
All refunds will be returned to the payer
of record, as identified on the FCC Form
159, unless the payer submits written
authorization instructing otherwise.
Federal Communications Commission.
Gary D. Michaels,
Deputy Chief, Auctions Spectrum and Access
Division, WTB.
[FR Doc. E8–10381 Filed 5–7–08; 8:45 am]
BILLING CODE 6712–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–08–0106]
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
Preventive Health and Health Services
Block Grant—Revision—National Center
for Chronic Disease and Public Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
The Preventive Health and Health
Services Block Grant program provides
awardees with their primary source of
flexible funding for health promotion
and disease prevention programs. Sixtyone awardees (50 states, the District of
Columbia, two American Indian Tribes,
and eight U.S. territories) currently
receive block grants from CDC in order
to address locally defined public health
needs in innovative ways. Block Grants
allow awardees to prioritize the use of
funds to fill funding gaps in programs
that deal with leading causes of death
and disability, as well as the ability to
respond rapidly to emerging health
issues.
CDC currently collects standardized
application and performance
information from each awardee through
an electronic Grant Application and
Reporting System (GARS). In response
to measures described in the
Government Performance Results Act,
CDC proposes to replace GARS with a
web-based Block Grant Management
Information System (BG-MIS) that will
collect information by the areas
described in Healthy People 2010 and
improve adherence to its goals.
Concurrent with conversion to the BGMIS, minor changes to the questions
and response options, and other
features, will be implemented to reduce
respondent burden and support the
Healthy People 2010 framework. These
features include increased utilization of
pre-defined response options, start and
end dates, the SMART (Specific,
Measurable, Achievable, Realistic, and
Time-based) format for describing
objectives, and identification of
Evidence Based Guidelines and Best
Practices used as the basis for public
health programs and interventions. In
addition, a Compliance Review section
has been added to provide each awardee
with general information regarding the
Compliance Review process and
specific information pertaining to its
past reviews.
Information will be collected twice
per year. Each awardee will submit an
annual Work Plan outlining awardeespecific health outcome objectives and
an Annual Report describing progress
toward its goals.
There are no costs to respondents
except their time. The estimated
annualized burden hours are 3,355.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Form name
PHHS Block Grant Awardees .........................
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Respondents
Work Plan .......................................................
Annual Report ................................................
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Number of
responses per
respondent
61
61
08MYN1
1
1
Average
burden per
response
(in hours)
25
30
26119
Federal Register / Vol. 73, No. 90 / Thursday, May 8, 2008 / Notices
Dated: April 30, 2008.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E8–10215 Filed 5–7–08; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2008–N–0063] (formerly
Docket No. 2008N–0016)
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Exports:
Notification and Recordkeeping
Requirements
AGENCY:
To ensure that comments on
the information collection are received,
OMB recommends that written
comments be faxed to the Office of
Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX:
202–395–6974, or e-mailed to
baguilar@omb.eop.gov. All comments
should be identified with the OMB
control number 0910–0482. Also
include the FDA docket number found
in brackets in the heading of this
document.
ADDRESSES:
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.
Food and Drug Administration,
HHS.
ACTION:
Fax written comments on the
collection of information by June 9,
2008.
DATES:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995.
In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
SUPPLEMENTARY INFORMATION:
Exports: Notification and
Recordkeeping Requirements—(OMB
Control Number 0910–0482)—Extension
The respondents to this information
collection are exporters who have
notified FDA of their intent to export
unapproved products that may not be
sold or marketed in the United States as
allowed under section 801(e) of the
Federal Food, Drug, and Cosmetic Act
(the act) (21 U.S.C. 381(e)). In general,
the notification identifies the product
being exported (e.g. name, description,
and in some cases, country of
destination) and specifies where the
notification should be sent. These
notifications are sent only for an initial
export; subsequent exports of the same
product to the same destination (or, in
the case of certain countries identified
in section 802(b) of the act (21 U.S.C.
382(b)), to any of those countries would
not result in a notification to FDA.
The recordkeepers to this information
collection are exporters who export
human drugs, biologics, devices, animal
drugs, foods and cosmetics that may not
be sold in the United States to maintain
records demonstrating their compliance
with the requirements in section
801(e)(1) of the act.
The total burden estimate of 39,120 is
based on the number of notifications
received by the relevant FDA centers in
fiscal year 2007, or the last year the
figures were available.
In the Federal Register of January 28,
2008 (73 FR 4874), FDA published a 60day notice requesting public comment
on the information collection
provisions. No comments were received.
TABLE 1.—ESTIMATED ANNUAL REPORTING BURDEN1
No. of
Respondents
21 CFR Section
1.101(d) and (e)
1 There
Annual Frequency
per Response
400
Total Annual
Responses
3
Hours per
Response
1,200
Total Hours
15
18,000
are no capital costs or operating and maintenance costs associated with this collection of information.
TABLE 2.—ESTIMATED ANNUAL RECORDKEEPING BURDEN1
1.101(b) and (c)
1 There
Annual Frequency
per
Recordkeeping
No. of
Recordkeepers
21 CFR Section
320
3
Hours per
Record
960
Total Hours
22
21,120
are no capital costs or operating and maintenance costs associated with this collection of information.
Dated: May 1, 2008.
Jeffrey Shuren,
Associate Commissioner for Policy and
Planning.
[FR Doc. E8–10204 Filed 5–7–08; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
Anti-Infective Drugs Advisory
Committee; Notice of Meeting
AGENCY:
mstockstill on PROD1PC66 with NOTICES
Total Annual
Records
Food and Drug Administration,
HHS.
ACTION:
Notice.
This notice announces a forthcoming
meeting of a public advisory committee
of the Food and Drug Administration
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(FDA). The meeting will be open to the
public.
Name of Committee: Anti-Infective
Drugs Advisory Committee.
General Function of the Committee:
To provide advice and
recommendations to the agency on
FDA’s regulatory issues.
Date and Time: The meeting will be
held on July 16, 2008, from 8 a.m. to 5
p.m.
Location: Food and Drug
Administration, Center for Drug
Evaluation and Research Advisory
E:\FR\FM\08MYN1.SGM
08MYN1
]]>Agencies
[Federal Register Volume 73, Number 90 (Thursday, May 8, 2008)]
[Notices]
[Pages 26118-26119]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-10215]
=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-08-0106]
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
Preventive Health and Health Services Block Grant--Revision--
National Center for Chronic Disease and Public Health Promotion
(NCCDPHP), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
The Preventive Health and Health Services Block Grant program
provides awardees with their primary source of flexible funding for
health promotion and disease prevention programs. Sixty-one awardees
(50 states, the District of Columbia, two American Indian Tribes, and
eight U.S. territories) currently receive block grants from CDC in
order to address locally defined public health needs in innovative
ways. Block Grants allow awardees to prioritize the use of funds to
fill funding gaps in programs that deal with leading causes of death
and disability, as well as the ability to respond rapidly to emerging
health issues.
CDC currently collects standardized application and performance
information from each awardee through an electronic Grant Application
and Reporting System (GARS). In response to measures described in the
Government Performance Results Act, CDC proposes to replace GARS with a
web-based Block Grant Management Information System (BG-MIS) that will
collect information by the areas described in Healthy People 2010 and
improve adherence to its goals. Concurrent with conversion to the BG-
MIS, minor changes to the questions and response options, and other
features, will be implemented to reduce respondent burden and support
the Healthy People 2010 framework. These features include increased
utilization of pre-defined response options, start and end dates, the
SMART (Specific, Measurable, Achievable, Realistic, and Time-based)
format for describing objectives, and identification of Evidence Based
Guidelines and Best Practices used as the basis for public health
programs and interventions. In addition, a Compliance Review section
has been added to provide each awardee with general information
regarding the Compliance Review process and specific information
pertaining to its past reviews.
Information will be collected twice per year. Each awardee will
submit an annual Work Plan outlining awardee-specific health outcome
objectives and an Annual Report describing progress toward its goals.
There are no costs to respondents except their time. The estimated
annualized burden hours are 3,355.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per
Respondents Form name respondents responses per response (in
respondent hours)
----------------------------------------------------------------------------------------------------------------
PHHS Block Grant Awardees............. Work Plan............... 61 1 25
Annual Report........... 61 1 30
----------------------------------------------------------------------------------------------------------------
[[Page 26119]]
Dated: April 30, 2008.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E8-10215 Filed 5-7-08; 8:45 am]
BILLING CODE 4163-18-P
