Agency Information Collection Request; 60-Day Public Comment Request, 71037 [2011-29562]

Download as PDF 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]


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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
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