Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; General Licensing Provisions: Biologics License Application, Changes to an Approved Application, Labeling, Revocation and Suspension, Postmarketing Studies Status Reports, and Forms FDA 356h and 2567; Correction, 7437 [E7-2576]
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7437
Federal Register / Vol. 72, No. 31 / Thursday, February 15, 2007 / Notices
costs other than the amount of time
required to respond to the survey.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of respondents
Data collection instrument
Average burden per response
(in hrs)
Responses/
respondent
Average annual burden
hours
Satisfaction survey (callers) .............................................................................
Satisfaction survey (e-mail inquiries) ...............................................................
Follow up survey ..............................................................................................
Key informant survey .......................................................................................
Postcard survey for bulk mailing .....................................................................
Postcard survey for individual publications .....................................................
Web survey for e-mail publication orders ........................................................
Web survey for internet publications ...............................................................
Special event/Outreach survey—General Public ............................................
Special event/Outreach survey—Professionals ...............................................
Emergency response survey—Level 1 emergency—General Public .............
Emergency response survey—Level 1 emergency—Professionals ................
Emergency response survey—Level 2 emergency—General Public .............
Emergency response survey—Level 2 emergency—Professionals ................
Emergency response survey—Level 3 emergency—General Public .............
Emergency response survey—Level 3 emergency—Professional .................
Emergency response survey—Level 4 emergency—General Public .............
Emergency response survey—Level 4 emergency—Professional .................
25,000
330
3,125
100
950
2,100
1,000
950
25,600
10,400
31,151
7,459
57,579
51,821
351,863
316,678
645,630
596,504
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
3/60
3/60
7/60
7/60
1/60
1/60
1/60
1/60
5/60
5/60
5/60
5/60
5/60
5/60
5/60
5/60
5/60
5/60
1,250
17
365
12
16
35
17
16
2,133
867
2596
622
4798
4318
29,322
26,390
53,803
49,709
Total Burden Hours ..................................................................................
........................
........................
........................
176,286
Dated: February 6, 2007.
Joan F. Karr,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E7–2637 Filed 2–14–07; 8:45 am]
BILLING CODE 4163–18–P
published with an error in titles
referring to an FDA form number in two
places in the document. This document
corrects those errors.
DATES:
February 15, 2007.
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
[Docket No. 2006N–0430]
In the
Federal Register of Friday, February 2,
2007, the following corrections are
made on page 5057:
1. In the first column, in the ninth
line of the title of the document, the
phrase ‘‘Forms FDA 456h’’ is corrected
to read ‘‘Forms FDA 356h’’.
2. In the second column, in the
SUPPLEMENTARY INFORMATION section of
the document, in the sixth line of the
title, the phrase ‘‘Forms FDA 456h’’ is
corrected to read ‘‘Forms FDA 356h’’.
SUPPLEMENTARY INFORMATION:
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; General Licensing
Provisions: Biologics License
Application, Changes to an Approved
Application, Labeling, Revocation and
Suspension, Postmarketing Studies
Status Reports, and Forms FDA 356h
and 2567; Correction
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is correcting a
notice that appeared in the Federal
Register of February 2, 2007 (72 FR
5057). The document announced that an
opportunity for public comment on a
proposed collection of information had
been submitted to the Office of
Management and Budget for review and
clearance under the Paperwork
Reduction Act of 1995. The notice
ycherry on PROD1PC64 with NOTICES
SUMMARY:
VerDate Aug<31>2005
18:37 Feb 14, 2007
Jkt 211001
Dated: February 8, 2007.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E7–2576 Filed 2–14–07; 8:45 am]
BILLING CODE 4160–01–S
PO 00000
Frm 00051
Fmt 4703
Sfmt 4703
Food and Drug Administration
[Docket No. 2006N–0436]
FOR FURTHER INFORMATION CONTACT:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Guidance for
Industry on How To Use E-Mail To
Submit a Study Protocol
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
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.
DATES: Fax written comments on the
collection of information by March 19,
2007.
ADDRESSES: 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.
FOR FURTHER INFORMATION CONTACT:
Denver Presley, Jr., Office of the Chief
Information Officer (HFA–250), Food
and Drug Administration, 5600 Fishers
E:\FR\FM\15FEN1.SGM
15FEN1
]]>Agencies
[Federal Register Volume 72, Number 31 (Thursday, February 15, 2007)]
[Notices]
[Page 7437]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-2576]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 2006N-0430]
Agency Information Collection Activities; Submission for Office
of Management and Budget Review; Comment Request; General Licensing
Provisions: Biologics License Application, Changes to an Approved
Application, Labeling, Revocation and Suspension, Postmarketing Studies
Status Reports, and Forms FDA 356h and 2567; Correction
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is correcting a notice
that appeared in the Federal Register of February 2, 2007 (72 FR 5057).
The document announced that an opportunity for public comment on a
proposed collection of information had been submitted to the Office of
Management and Budget for review and clearance under the Paperwork
Reduction Act of 1995. The notice published with an error in titles
referring to an FDA form number in two places in the document. This
document corrects those errors.
DATES: February 15, 2007.
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.
SUPPLEMENTARY INFORMATION: In the Federal Register of Friday, February
2, 2007, the following corrections are made on page 5057:
1. In the first column, in the ninth line of the title of the
document, the phrase ``Forms FDA 456h'' is corrected to read ``Forms
FDA 356h''.
2. In the second column, in the SUPPLEMENTARY INFORMATION section
of the document, in the sixth line of the title, the phrase ``Forms FDA
456h'' is corrected to read ``Forms FDA 356h''.
Dated: February 8, 2007.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E7-2576 Filed 2-14-07; 8:45 am]
BILLING CODE 4160-01-S
