Agency Information Collection Request; 60-Day Public Comment Request, 71037 [2011-29562]
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71037
Federal Register / Vol. 76, No. 221 / Wednesday, November 16, 2011 / Notices
ESTIMATED ANNUALIZED BURDEN TABLE
Type of
respondent
Forms
MFS–IP
MFS–IP
MFS–IP
MFS–IP
Follow-up
Follow-up
Follow-up
Follow-up
Survey—Fathers (9 & 18 month)
Survey—Partners (9 & 18 month)
Survey—Fathers (34 month) ........
Survey—Partners (34 month) .......
Totals ....................................................................
Keith A. Tucker,
Paperwork Reduction Act Reports Clearance
Officer, Office of the Secretary.
[FR Doc. 2011–29563 Filed 11–15–11; 8:45 am]
BILLING CODE 4150–05–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[Document Identifier OS–0990–0263]
Agency Information Collection
Request; 60-Day Public Comment
Request
Office of the Secretary.
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 information collection request
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
AGENCY:
Individuals
individuals
Individuals
Individuals
Number of
responses
per
respondent
Number of
respondents
Average
burden
(in hours)
per response
............
............
............
............
321
489
463
463
1
1
1
1
1.5
1.5
1.5
1.5
..............................
........................
........................
........................
Annual
burden
481.5
733.5
694.5
694.5
2604
[Section 103(a)]; and (2) certify to the
awarding department or agency that the
application or proposal for research has
been reviewed and approved by an IRB
designated in the assurance [Sections
103(b) and (f)]. The Office for Human
Research Protections is requesting a
three-year extension of the Protection of
Human Subjects: Assurance
Identification/IRB Certification/
Declaration of Exemption Form. That
form is designed to promote uniformity
among departments and agencies, and to
help ensure common means of
ascertaining institutional review board
certifications and other reporting
requirements relating to the protection
of human subjects in research.
Respondents are institutions engaged in
research involving human subjects
where the research is supported by
HHS. Institutional use of the form is
also relied upon by other federal
departments and agencies that have
codified or follow the Federal Policy for
the Protection of Human Subjects
(Common Rule). There are an estimated
total of 25,000 human research studies
supported each year, an average of 2
certifications per institutions and an
estimated one-half hour per
certification, for a total burden of 12,000
hours. Data is collected as needed.
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, email 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)
690–6162. Written comments and
recommendations for the proposed
information collections must be directed
to the OS Paperwork Clearance Officer
at the above email address within 60
days.
Proposed Project: Protection of
Human Subjects: Assurance
Identification/IRB Certification/
Declaration of Exemption Form—
Extension—OMB No. 0990–0263—
Office for Human Research Protections.
Abstract: The Federal Policy for the
Protection of Human Subjects, known as
the Common Rule, requires that before
engaging in non-exempt human subjects
research that is conducted or supported
by a Common Rule department or
agency, each institution must: (1) Hold
an applicable assurance of compliance
ESTIMATED ANNUALIZED BURDEN IN HOURS
Number of
respondents
Number of
responses per
respondent
Hours per
response
Response
burden hours
Protection of Human Subjects: Assurance Identification/IRB Certification/
Declaration of Exemption .............................................................................
mstockstill on DSK4VPTVN1PROD with NOTICES
Form name
12,000
2
0.5
12,000
Keith A. Tucker,
Paperwork Reduction Act Reports Clearance
Officer, Office of the Secretary.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[FR Doc. 2011–29562 Filed 11–15–11; 8:45 am]
Proposed National Toxicology
Program (NTP) Review Process for the
Report on Carcinogens: Request for
Public Comment and Listening
Session: Amended Notice
BILLING CODE 4150–36–P
Division of the National
Toxicology Program (DNTP), National
AGENCY:
VerDate Mar<15>2010
17:45 Nov 15, 2011
Jkt 226001
PO 00000
Frm 00084
Fmt 4703
Sfmt 4703
Institute of Environmental Health
Sciences (NIEHS); National Institutes of
Health (NIH).
Extension of time for the public
listing session and increase in the
number of oral presenters.
ACTION:
The NTP announces that the
public listening session on the proposed
review process for the Report on
SUMMARY:
E:\FR\FM\16NON1.SGM
16NON1
Agencies
[Federal Register Volume 76, Number 221 (Wednesday, November 16, 2011)]
[Notices]
[Page 71037]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-29562]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
[Document Identifier OS-0990-0263]
Agency Information Collection Request; 60-Day Public Comment
Request
AGENCY: Office of the Secretary.
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 information collection request 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, email 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) 690-6162. Written comments and
recommendations for the proposed information collections must be
directed to the OS Paperwork Clearance Officer at the above email
address within 60 days.
Proposed Project: Protection of Human Subjects: Assurance
Identification/IRB Certification/Declaration of Exemption Form--
Extension--OMB No. 0990-0263--Office for Human Research Protections.
Abstract: The Federal Policy for the Protection of Human Subjects,
known as the Common Rule, requires that before engaging in non-exempt
human subjects research that is conducted or supported by a Common Rule
department or agency, each institution must: (1) Hold an applicable
assurance of compliance [Section 103(a)]; and (2) certify to the
awarding department or agency that the application or proposal for
research has been reviewed and approved by an IRB designated in the
assurance [Sections 103(b) and (f)]. The Office for Human Research
Protections is requesting a three-year extension of the Protection of
Human Subjects: Assurance Identification/IRB Certification/Declaration
of Exemption Form. That form is designed to promote uniformity among
departments and agencies, and to help ensure common means of
ascertaining institutional review board certifications and other
reporting requirements relating to the protection of human subjects in
research. Respondents are institutions engaged in research involving
human subjects where the research is supported by HHS. Institutional
use of the form is also relied upon by other federal departments and
agencies that have codified or follow the Federal Policy for the
Protection of Human Subjects (Common Rule). There are an estimated
total of 25,000 human research studies supported each year, an average
of 2 certifications per institutions and an estimated one-half hour per
certification, for a total burden of 12,000 hours. Data is collected as
needed.
Estimated Annualized Burden in Hours
----------------------------------------------------------------------------------------------------------------
Number of
Form name Number of responses per Hours per Response
respondents respondent response burden hours
----------------------------------------------------------------------------------------------------------------
Protection of Human Subjects: Assurance 12,000 2 0.5 12,000
Identification/IRB Certification/
Declaration of Exemption...................
----------------------------------------------------------------------------------------------------------------
Keith A. Tucker,
Paperwork Reduction Act Reports Clearance Officer, Office of the
Secretary.
[FR Doc. 2011-29562 Filed 11-15-11; 8:45 am]
BILLING CODE 4150-36-P