Submission for OMB Review; Comment Request, 12733-12734 [2016-05291]

Download as PDF 12733 Federal Register / Vol. 81, No. 47 / Thursday, March 10, 2016 / Notices There will be a number of hazards included in each image. The participant will be asked to search for and find the hazards. During the study, all 62 participants will be asked to search pictures. The participants will wear a light weight eye-tracking system so that eye-movements can be collected and search patterns can be mapped during respondent to complete. All 62 respondents will then complete the Risk Assessment Measure (time to complete, 20 minutes), the Risk Propensity Scale (time to complete, 6 minutes), the Mine Specific Risk Tolerance Measure (time to complete, 6 minutes), and the Openended Questions (time to complete, 30 minutes). analysis to determine differences based on level of experience. Identification accuracy will also be collected to determine whether level of experience affects the number of hazards identified. After the laboratory study is complete, all 62 respondents will complete the demographic questionnaire. This should take approximately six minutes for each ESTIMATED ANNUALIZED BURDEN HOURS Form name Mine Employee ............................................... Safety Professional ......................................... Student ............................................................ Mine Employee ............................................... Safety Professional ......................................... Student ............................................................ Mine Employee ............................................... Safety Professional ......................................... Student ............................................................ Mine Employee ............................................... Safety Professional ......................................... Student ............................................................ Mine Employee ............................................... Safety Professional ......................................... Student ............................................................ Mine Employee ............................................... Safety Professional ......................................... Student ............................................................ Mine Employee ............................................... Safety Professional ......................................... Student ............................................................ Prescreening Questionnaire ........................... ......................................................................... ......................................................................... Demographic Questionnaire .......................... ......................................................................... ......................................................................... Experimental Task ......................................... ......................................................................... ......................................................................... Risk Assessment Measure ............................ ......................................................................... ......................................................................... Risk Propensity Scale .................................... ......................................................................... ......................................................................... Mine Specific Risk Tolerance Measure ......... ......................................................................... ......................................................................... Open Ended Questions .................................. ......................................................................... ......................................................................... Leroy A. Richardson, Chief, Information Collection Review Office Office of Scientific Integrity Office of the Associate Director for Science Office of the Director Centers for Disease Control and Prevention. [FR Doc. 2016–05358 Filed 3–9–16; 8:45 am] BILLING CODE 4163–18–P Number responses per respondent Number of respondents Type of respondent DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for OMB Review; Comment Request Title: ANA Project Impact Assessment Survey. OMB No.: 0970–0379. Description: The information collected by the Project Impact Assessment Survey is needed for two main reasons: (1) To collect crucial information required to report on the Administration for Native Americans’ (ANA) established Government Performance and Results Act (GPRA) 23 10 10 15 8 8 15 8 8 15 8 8 15 8 8 15 8 8 15 8 8 Average burden per response (in hours) 1 15/60 1 6/60 1 1 1 20/60 1 6/60 1 6/60 1 30/60 measures, and (2) to properly abide by ANA’s congressionally-mandated statute (42 United States Code 2991 et seq.) found within the Native American Programs Act of 1974, as amended, which states that ANA will evaluate projects assisted through ANA grant dollars ‘‘including evaluations that describe and measure the impact of such projects, their effectiveness in achieving stated goals, their impact on related programs, and their structure and mechanisms for delivery of services.’’ The information collected with this survey will fulfill ANA’s statutory requirement and will also serve as an important planning and performance tool for ANA. Respondents mstockstill on DSK4VPTVN1PROD with NOTICES ANNUAL BURDEN ESTIMATES Number of respondents Instrument Number of responses per respondent Average burden hours per response Total burden hours ANA Project Impact Assessment Survey ........................................................ 85 1 6 510 Estimated Total Annual Burden Hours ..................................................... ........................ ........................ ........................ 510 VerDate Sep<11>2014 17:55 Mar 09, 2016 Jkt 238001 PO 00000 Frm 00054 Fmt 4703 Sfmt 4703 E:\FR\FM\10MRN1.SGM 10MRN1 12734 Federal Register / Vol. 81, No. 47 / Thursday, March 10, 2016 / Notices 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, 330 C Street SW., Washington, DC 20201. Attention Reports Clearance Officer. All requests should be identified by the title of the information collection. Email address: infocollection@acf.hhs.gov. 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, Email: OIRA_ SUBMISSION@OMB.EOP.GOV, Attn: Desk Officer for the Administration for Children and Families. Robert Sargis, Reports Clearance Officer. [FR Doc. 2016–05291 Filed 3–9–16; 8:45 am] BILLING CODE 4184–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2010–D–0319] Agency Information Collection Activities; Comment Request; Guidance for Industry and Food and Drug Administration Staff on Dear Health Care Provider Letters: Improving Communication of Important Safety Information AGENCY: Food and Drug Administration, HHS. ACTION: Notice. 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 an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on the information collection associated mstockstill on DSK4VPTVN1PROD with NOTICES SUMMARY: VerDate Sep<11>2014 17:55 Mar 09, 2016 Jkt 238001 with the guidance for industry and FDA staff entitled ‘‘Dear Health Care Provider Letters: Improving Communication of Important Safety Information.’’ This guidance offers specific recommendations to industry on the content and format of Dear Health Care Provider (DHCP) letters. These letters are sent by manufacturers or distributors to health care providers to communicate an important drug warning, a change in prescribing information, or a correction of misinformation in prescription drug promotional labeling or advertising. This guidance provides recommendations on when to use a DHCP letter, the types of information to include in the DHCP letter, how to organize the information so that it is communicated effectively to health care providers, and formatting techniques to make the information more accessible. DATES: Submit either electronic or written comments on the collection of information by May 9, 2016. ADDRESSES: You may submit comments as follows: Electronic Submissions Submit electronic comments in the following way: • Federal eRulemaking Portal: http:// www.regulations.gov. Follow the instructions for submitting comments. Comments submitted electronically, including attachments, to http:// www.regulations.gov will be posted to the docket unchanged. Because your comment will be made public, you are solely responsible for ensuring that your comment does not include any confidential information that you or a third party may not wish to be posted, such as medical information, your or anyone else’s Social Security number, or confidential business information, such as a manufacturing process. Please note that if you include your name, contact information, or other information that identifies you in the body of your comments, that information will be posted on http://www.regulations.gov. • If you want to submit a comment with confidential information that you do not wish to be made available to the public, submit the comment as a written/paper submission and in the manner detailed (see ‘‘Written/Paper Submissions’’ and ‘‘Instructions’’). Written/Paper Submissions Submit written/paper submissions as follows: • Mail/Hand delivery/Courier (for written/paper submissions): Division of Dockets Management (HFA–305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. PO 00000 Frm 00055 Fmt 4703 Sfmt 4703 • For written/paper comments submitted to the Division of Dockets Management, FDA will post your comment, as well as any attachments, except for information submitted, marked and identified, as confidential, if submitted as detailed in ‘‘Instructions.’’ Instructions: All submissions received must include the Docket No. FDA– 2010–D–0319 for Guidance for Industry and Food and Drug Administration Staff on Dear Health Care Provider Letters: Improving Communication of Important Safety Information. Received comments will be placed in the docket and, except for those submitted as ‘‘Confidential Submissions,’’ publicly viewable at http://www.regulations.gov or at the Division of Dockets Management between 9 a.m. and 4 p.m., Monday through Friday. • Confidential Submissions—To submit a comment with confidential information that you do not wish to be made publicly available, submit your comments only as a written/paper submission. You should submit two copies total. One copy will include the information you claim to be confidential with a heading or cover note that states ‘‘THIS DOCUMENT CONTAINS CONFIDENTIAL INFORMATION’’. The Agency will review this copy, including the claimed confidential information, in its consideration of comments. The second copy, which will have the claimed confidential information redacted/blacked out, will be available for public viewing and posted on http://www.regulations.gov. Submit both copies to the Division of Dockets Management. If you do not wish your name and contact information to be made publicly available, you can provide this information on the cover sheet and not in the body of your comments and you must identify this information as ‘‘confidential.’’ Any information marked as ‘‘confidential’’ will not be disclosed except in accordance with 21 CFR 10.20 and other applicable disclosure law. For more information about FDA’s posting of comments to public dockets, see 80 FR 56469, September 18, 2015, or access the information at: http://www.fda.gov/ regulatoryinformation/dockets/ default.htm. Docket: For access to the docket to read background documents or the electronic and written/paper comments received, go to http:// www.regulations.gov and insert the docket number, found in brackets in the heading of this document, into the ‘‘Search’’ box and follow the prompts and/or go to the Division of Dockets E:\FR\FM\10MRN1.SGM 10MRN1

Agencies

[Federal Register Volume 81, Number 47 (Thursday, March 10, 2016)]
[Notices]
[Pages 12733-12734]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-05291]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Submission for OMB Review; Comment Request

    Title: ANA Project Impact Assessment Survey.
    OMB No.: 0970-0379.
    Description: The information collected by the Project Impact 
Assessment Survey is needed for two main reasons: (1) To collect 
crucial information required to report on the Administration for Native 
Americans' (ANA) established Government Performance and Results Act 
(GPRA) measures, and (2) to properly abide by ANA's congressionally-
mandated statute (42 United States Code 2991 et seq.) found within the 
Native American Programs Act of 1974, as amended, which states that ANA 
will evaluate projects assisted through ANA grant dollars ``including 
evaluations that describe and measure the impact of such projects, 
their effectiveness in achieving stated goals, their impact on related 
programs, and their structure and mechanisms for delivery of 
services.'' The information collected with this survey will fulfill 
ANA's statutory requirement and will also serve as an important 
planning and performance tool for ANA.

Respondents

                                             Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
                                                                     Number of        Average
                   Instrument                        Number of     responses per   burden hours    Total burden
                                                    respondents     respondent     per response        hours
----------------------------------------------------------------------------------------------------------------
ANA Project Impact Assessment Survey............              85               1               6             510
                                                                                                 ---------------
    Estimated Total Annual Burden Hours.........  ..............  ..............  ..............             510
----------------------------------------------------------------------------------------------------------------


[[Page 12734]]

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, 330 C Street SW., Washington, DC 20201. Attention 
Reports Clearance Officer. All requests should be identified by the 
title of the information collection. Email address: 
infocollection@acf.hhs.gov.

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, Email: 
OIRA_SUBMISSION@OMB.EOP.GOV, Attn: Desk Officer for the Administration 
for Children and Families.

Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2016-05291 Filed 3-9-16; 8:45 am]
BILLING CODE 4184-01-P