Agency Information Collection Request. 30-Day Public Comment Request, 55555-55556 [E9-25936]
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55555
Federal Register / Vol. 74, No. 207 / Wednesday, October 28, 2009 / Notices
ESTIMATED ANNUALIZED BURDEN TABLE
Number of
responses per
respondent
Number of
respondents
Average
burden hours
per response
Total burden
hours
Forms
Type of respondent
Screening Form ................................
22,845
1
2/60
761
Interview Form ..................................
Non-Participating
Household
(Screened).
Eligible Household (Completes Survey).
2,570
1
14/60
600
Total ...........................................
...........................................................
........................
........................
........................
1361
Seleda Perryman,
Office of the Secretary, Paperwork Reduction
Act Reports Clearance Officer.
[FR Doc. E9–25935 Filed 10–27–09; 8:45 am]
BILLING CODE 4150–45–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[Document Identifier: OS–0937–0166; 30day notice]
Agency Information Collection
Request. 30-Day Public Comment
Request
Office of the Secretary, HHS.
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 a
proposed collection 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,
AGENCY:
information to assure voluntary and
informed consent to persons undergoing
sterilization in programs of health
services which are supported by Federal
financial assistance administered by the
Public Health Service (PHS). The form
provides additional procedural
protections to individuals undergoing
sterilization. In order to obtain informed
consent, the regulation requires that
programs use either the form that is
appended to the PHS regulation or
another consent form approved by the
Secretary.
In 2003, the sterilization consent form
was revised to conform to OMB
government-wide standards for the
collection of race/ethnicity data and to
incorporate the PRA burden statement
as part of the consent form. The current
form has been updated to conform to the
changed name of a federal entitlement
program. The program, Aid to Families
with Dependent Children (AFDC),
utilized by low-income families with
dependent children who need federal
assistance, has been replaced by a
different program with similar aims,
Temporary Assistance for Needy
Families (TANF). Consequently, the
reference to AFDC in the first paragraph
has been replaced with a reference to
TANF.
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.
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, e-mail your request,
including your address, phone number,
OMB number, and OS document
identifier, to
Sherette.funncoleman@hhs.gov, or call
the Reports Clearance Office on (202)
690–5683. Send written comments and
recommendations for the proposed
information collections within 30 days
of this notice directly to the OS OMB
Desk Officer; faxed to OMB at 202–395–
5806.
Proposed Project: HHS 42 CFR part
50, subpart B; Sterilization of Persons in
Federally Assisted Family Planning
Projects—OMB No. 0937–0166Revision-Office of Population Affairs—
Office of Family Planning.
Abstract: This is a request for revision
of a currently approved collection for
the disclosure and record-keeping
requirements codified at 42 CFR part 50,
subpart B (‘‘Sterilization of Persons in
Federally Assisted Family Planning
Projects’’). The consent form solicits
ESTIMATED ANNUALIZED BURDEN TABLE
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
Form name
Citizens Seeking Sterilization ...........
Information Disclosure for Sterilization Consent Form.
Record-keeping
for
Sterilization
Consent Form.
100,000
1
1
100,000
Citizens Seeking Sterilization ...........
100,000
1
15/60
25,000
Total ...........................................
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Type of respondent
...........................................................
........................
........................
........................
125,000
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55556
Federal Register / Vol. 74, No. 207 / Wednesday, October 28, 2009 / Notices
Seleda Perryman,
Office of the Secretary, Paperwork Reduction
Act Reports Clearance Officer.
[FR Doc. E9–25936 Filed 10–27–09; 8:45 am]
BILLING CODE 4150–34–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2009–N–0511]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Medicated Feed
Mill License Application
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing an
opportunity for public comment on the
proposed collection of certain
information by the agency. Under the
Paperwork Reduction Act of 1995 (the
PRA), Federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension of a collection of information
and to allow 60 days for public
comment in response to the notice. This
notice solicits comments on the
medicated feed mill licensing
applications.
DATES: Submit written or electronic
comments on the collection of
information by December 28, 2009.
ADDRESSES: Submit electronic
comments on the collection of
information to https://www.
regulations.gov. Submit written
comments on the collection of
information to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. All
comments should be identified with the
docket number found in brackets in the
heading of this document.
FOR FURTHER INFORMATION CONTACT:
Denver Presley, Jr., Office of Information
Management (HFA–710), Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301–796–3793.
SUPPLEMENTARY INFORMATION: Under the
PRA (44 U.S.C. 3501–3520), Federal
agencies must obtain approval from the
Office of Management and Budget
(OMB) for each collection of
information they conduct or sponsor.
‘‘Collection of information’’ is defined
in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA (44
U.S.C. 3506(c)(2)(A)) requires Federal
agencies to provide a 60-day notice in
the Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information,
before submitting the collection to OMB
for approval. To comply with this
requirement, FDA is publishing notice
of the proposed collection of
information set forth in this document.
With respect to the following
collection of information, FDA invites
comments on these topics: (1) Whether
the proposed collection of information
is necessary for the proper performance
of FDA’s functions, including whether
the information will have practical
utility; (2) the accuracy of FDA’s
estimate of the burden of the proposed
collection of information, including the
validity of the methodology and
assumptions used; (3) ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques,
when appropriate, and other forms of
information technology.
Medicated Feed Mill License
Application—21 CFR Part 515 (OMB
Control Number 0910–0337)—Extension
The Animal Drug Availability Act
(ADAA) of October 9, 1996, amended
section 512 of the Federal Food, Drug,
and Cosmetic Act (the act) (21 U.S.C.
360b) to replace the system for the
approval of specific medicated feed
with a general licensing system for feed
mills. Before passage of the ADAA,
medicated feed manufacturers were
required to obtain approval of
Medicated Feed Applications (MFAs),
in order to manufacture certain types of
medicated feeds. An individual
approved MFA was required for each
and every applicable medicated feed.
The ADAA streamlined the paperwork
process for gaining approval to
manufacture medicated feeds by
replacing the MFA system with a
facility license for each medicated feed
manufacturing facility.
FDA estimates the burden of this
collection of information as follows:
TABLE 1.—ESTIMATED ANNUAL REPORTING BURDEN1
21 CFR Section
No. of
Respondents
Annual Frequency
per Response
Total Annual
Responses
Hours per
Response
Total Hours
515.10(b)
20
1
20
0.25
5
515.11(b)
75
1
75
0.25
18.75
515.23
40
1
40
0.25
10
0.15
1
0.15
24
3.6
515.30(c)
Total Burden Hours
1 There
37.35
are no capital or operating and maintenance costs associated with this collection of information.
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TABLE 2.—ESTIMATED ANNUAL RECORDKEEPING BURDEN1
21 CFR Section
No. of
Recordkeepers
510.305
1 There
Annual Frequency
per Recordkeeping
1,070
Total Annual
Records
1
Hours per
Record
1,070
0.03
are no capital or operating and maintenance costs associated with this collection of information.
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]]>Agencies
[Federal Register Volume 74, Number 207 (Wednesday, October 28, 2009)]
[Notices]
[Pages 55555-55556]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-25936]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
[Document Identifier: OS-0937-0166; 30-day notice]
Agency Information Collection Request. 30-Day Public Comment
Request
AGENCY: Office of the Secretary, HHS.
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 a proposed collection 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.
To obtain copies of the supporting statement and any related forms
for the proposed paperwork collections referenced above, e-mail your
request, including your address, phone number, OMB number, and OS
document identifier, to Sherette.funncoleman@hhs.gov, or call the
Reports Clearance Office on (202) 690-5683. Send written comments and
recommendations for the proposed information collections within 30 days
of this notice directly to the OS OMB Desk Officer; faxed to OMB at
202-395-5806.
Proposed Project: HHS 42 CFR part 50, subpart B; Sterilization of
Persons in Federally Assisted Family Planning Projects--OMB No. 0937-
0166- Revision-Office of Population Affairs--Office of Family Planning.
Abstract: This is a request for revision of a currently approved
collection for the disclosure and record-keeping requirements codified
at 42 CFR part 50, subpart B (``Sterilization of Persons in Federally
Assisted Family Planning Projects''). The consent form solicits
information to assure voluntary and informed consent to persons
undergoing sterilization in programs of health services which are
supported by Federal financial assistance administered by the Public
Health Service (PHS). The form provides additional procedural
protections to individuals undergoing sterilization. In order to obtain
informed consent, the regulation requires that programs use either the
form that is appended to the PHS regulation or another consent form
approved by the Secretary.
In 2003, the sterilization consent form was revised to conform to
OMB government-wide standards for the collection of race/ethnicity data
and to incorporate the PRA burden statement as part of the consent
form. The current form has been updated to conform to the changed name
of a federal entitlement program. The program, Aid to Families with
Dependent Children (AFDC), utilized by low-income families with
dependent children who need federal assistance, has been replaced by a
different program with similar aims, Temporary Assistance for Needy
Families (TANF). Consequently, the reference to AFDC in the first
paragraph has been replaced with a reference to TANF.
Estimated Annualized Burden Table
----------------------------------------------------------------------------------------------------------------
Number of Average
Type of respondent Form name Number of responses per burden per Total hours
respondents respondent response
----------------------------------------------------------------------------------------------------------------
Citizens Seeking Sterilization Information 100,000 1 1 100,000
Disclosure for
Sterilization
Consent Form.
Citizens Seeking Sterilization Record-keeping 100,000 1 15/60 25,000
for
Sterilization
Consent Form.
---------------------------------------------------------------------------------
Total..................... ................ .............. .............. .............. 125,000
----------------------------------------------------------------------------------------------------------------
[[Page 55556]]
Seleda Perryman,
Office of the Secretary, Paperwork Reduction Act Reports Clearance
Officer.
[FR Doc. E9-25936 Filed 10-27-09; 8:45 am]
BILLING CODE 4150-34-P
