Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Exceptions or Alternatives to Labeling Requirements for Products Held by the Strategic National Stockpile, 39964 [E8-15795]
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39964
Federal Register / Vol. 73, No. 134 / Friday, July 11, 2008 / Notices
Respondents: Executive directors and
key staff of faith based and community
organizations that received three-year
CEY grants beginning in 2007.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
Lead Organization Executive Director .............................................................
Lead Organization Key Staff ...........................................................................
Partner Organization Executive Director .........................................................
Partner Organization Key Staff ........................................................................
Estimated Total Annual Burden
Hours: 445.
Additional Information: Copies of the
proposed collection may be obtained by
writing to the Administration for
Children and Families, Office of
Planning, Research and Evaluation, 370
L’Enfant Promenade, SW., Washington,
DC 20447, Attn: ACF Reports Clearance
Officer. E-mail address:
OPREInfoCollection@acf.hhs.gov. All
requests should be identified by the title
of the information collection.
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 ACF.
Dated: July 2, 2008.
Brendan C. Kelly,
OPRE Reports Clearance Officer.
[FR Doc. E8–15502 Filed 7–10–08; 8:45 am]
BILLING CODE 4184–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
pwalker on PROD1PC71 with NOTICES
[Docket No. FDA–2006–N–0364] (formerly
Docket Nos. 2006N–0466 and FDA–2007–
0650)
FOR FURTHER INFORMATION CONTACT:
Jonna Capezzuto, Office of the Chief
Information Officer (HFA–710), Food
and Drug Administration, 5600 Fishers
Lane, Rockville, MD 20857, 301–796–
3794.
In the
Federal Register of December 28, 2007
(72 FR 73589), the agency announced
that the proposed information collection
had been submitted to OMB for review
and clearance under 44 U.S.C. 3507. An
agency may not conduct or sponsor, and
a person is not required to respond to,
a collection of information unless it
displays a currently valid OMB control
number. OMB has now approved the
information collection and has assigned
OMB control number 0910–0614. The
approval expires on June 30, 2011. A
copy of the supporting statement for this
information collection is available on
the Internet at https://www.reginfo.gov/
public/do/PRAMain.
SUPPLEMENTARY INFORMATION:
Dated: July 2, 2008.
Jeffrey Shuren,
Associate Commissioner for Policy and
Planning.
[FR Doc. E8–15795 Filed 7–10–08; 8:45 am]
Agency Information Collection
Activities; Announcement of Office of
Management and Budget Approval;
Exceptions or Alternatives to Labeling
Requirements for Products Held by the
Strategic National Stockpile
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
VerDate Aug<31>2005
17:19 Jul 10, 2008
Jkt 214001
10
20
60
60
SUMMARY: The Food and Drug
Administration (FDA) is announcing
that a collection of information entitled
‘‘Exceptions or Alternatives to Labeling
Requirements for Products Held by the
Strategic National Stockpile’’ has been
approved by the Office of Management
and Budget (OMB) under the Paperwork
Reduction Act of 1995.
BILLING CODE 4160–01–S
PO 00000
Frm 00027
Fmt 4703
Sfmt 4703
Number of
responses
per respondent
Average
burden hours
per response
1
1
1
1
Total burden
hours
3.5
2.5
3.5
2.5
35
50
210
150
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2005–N–0464] (formerly
Docket No. 2005N–0403)
Draft Guidance for Industry on
Providing Regulatory Submissions in
Electronic Format—Drug
Establishment Registration and Drug
Listing; Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing the
availability of a draft guidance for
industry entitled ‘‘Providing Regulatory
Submissions in Electronic Format—
Drug Establishment Registration and
Drug Listing.’’ This draft guidance
document establishes a Pilot Program
for industry to voluntarily submit drug
establishment registration and drug
listing information in an electronic
format that FDA can process, review,
and archive. The document provides
guidance on what required and FDArecommended information related to
drug establishment registration and drug
listing to submit and on how to
electronically prepare and submit the
information to FDA.
DATES: Although you can comment on
any guidance at any time (see 21 CFR
10.115(g)(5)), to ensure that the agency
considers your comments on this draft
guidance before it begins work on the
final version of the guidance, submit
written or electronic comments on the
draft guidance, including comments
regarding proposed collection of
information, by September 9, 2008.
ADDRESSES: Submit written requests for
single copies of the draft guidance to the
Office of Critical Path Programs (HF–
18), Office of the Commissioner, Food
and Drug Administration, 5600 Fishers
Lane, Rockville, MD 20857. Send one
self-addressed adhesive label to assist
the office in processing your requests.
E:\FR\FM\11JYN1.SGM
11JYN1
]]>Agencies
[Federal Register Volume 73, Number 134 (Friday, July 11, 2008)]
[Notices]
[Page 39964]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-15795]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2006-N-0364] (formerly Docket Nos. 2006N-0466 and FDA-
2007-0650)
Agency Information Collection Activities; Announcement of Office
of Management and Budget Approval; Exceptions or Alternatives to
Labeling Requirements for Products Held by the Strategic National
Stockpile
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing that a
collection of information entitled ``Exceptions or Alternatives to
Labeling Requirements for Products Held by the Strategic National
Stockpile'' has been approved by the Office of Management and Budget
(OMB) under the Paperwork Reduction Act of 1995.
FOR FURTHER INFORMATION CONTACT: Jonna Capezzuto, Office of the Chief
Information Officer (HFA-710), Food and Drug Administration, 5600
Fishers Lane, Rockville, MD 20857, 301-796-3794.
SUPPLEMENTARY INFORMATION: In the Federal Register of December 28, 2007
(72 FR 73589), the agency announced that the proposed information
collection had been submitted to OMB for review and clearance under 44
U.S.C. 3507. An agency may not conduct or sponsor, and a person is not
required to respond to, a collection of information unless it displays
a currently valid OMB control number. OMB has now approved the
information collection and has assigned OMB control number 0910-0614.
The approval expires on June 30, 2011. A copy of the supporting
statement for this information collection is available on the Internet
at https://www.reginfo.gov/public/do/PRAMain.
Dated: July 2, 2008.
Jeffrey Shuren,
Associate Commissioner for Policy and Planning.
[FR Doc. E8-15795 Filed 7-10-08; 8:45 am]
BILLING CODE 4160-01-S
