Proposed Information Collection Activity; Comment Request, 31942-31943 [2013-12588]

Download as PDF 31942 Federal Register / Vol. 78, No. 102 / Tuesday, May 28, 2013 / Notices ANNUAL BURDEN ESTIMATES—Continued Instrument Annual number of respondents Number of responses per respondent Average burden hours per response DCFS Biological Parent Interview ........................................... DCFS Youth and Foster Parent Study Contact Form ............. DCFS Foster Parent Interview ................................................ DCFS Youth Interview ............................................................. DCFS burden .................................................................... RISE Staff Pre-Test ................................................................. RISE Staff Post-Test ............................................................... RISE burden ..................................................................... 173 1 228 228 .............................. 157 157 .............................. 2 228 2 2 .............................. 1 1 .............................. .25 .1 .75 .75 .............................. .25 .25 .............................. Estimated Total Annual Burden Hours: 888 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, 370 L’Enfant Promenade SW., Washington, DC 20447, Attn: OPRE Reports Clearance Officer. All requests should be identified by the title of the information collection. Email address: OPREinfocollection@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. Steven M. Hanmer, OPRE Reports Clearance Officer. [FR Doc. 2013–12546 Filed 5–24–13; 8:45 am] BILLING CODE 4184–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families mstockstill on DSK4VPTVN1PROD with NOTICES Proposed Information Collection Activity; Comment Request Title: Parents and Children Together (PACT) Evaluation. OMB No.: 0970–0403. Description: The Office of Planning, Research, and Evaluation (OPRE), Administration for Children and Families (ACF), U.S. Department of Health and Human Services (HHS), is proposing data collection activity as VerDate Mar<15>2010 17:46 May 24, 2013 Jkt 229001 part of the Parents and Children Together (PACT) Evaluation. The objective of the PACT evaluation is to document and provide initial assessment of selected Responsible Fatherhood and Healthy Marriage grant programs that were authorized under the 2010 Claims Resolution Act. This information will be critical to informing decisions related to future investments in programming as well as the design and operation of such services. PACT is utilizing three major, interrelated evaluation strategies: Impact evaluation; implementation evaluation; and qualitative evaluation. To collect data for these strategies, four instruments have been approved todate, and 14 new instruments are under review as of the publish date of this notice. Instruments approved to-date: (1) Selecting Study Grantees (discussions with program and partner organization staff)—APPROVED April 20, 2012. (2) Introductory Script (for RF program staff to discuss with program applicants)—APPROVED October 31, 2012. (3) Baseline Survey (for RF study participants)—APPROVED October 31, 2012. (4) RF study Management Information System (MIS)—APPROVED October 31, 2012. Instruments under review at publish date of this notice: (5) Introductory Script (for HM program staff to discuss with program applicants). (6) Baseline Survey (for HM study participants). (7) HM study Management Information System (MIS) (8) Semistructured interview topic guide (for program staff). (9) On-line survey (for program staff). (10) Telephone interview guide (for program staff at referral organizations). (11) On-line Working Alliance Inventory (for program staff and participants). PO 00000 Frm 00059 Fmt 4703 Sfmt 4703 Totalannual burden hours 86 23 342 342 810 39 39 78 (12) Focus group discussion guide (for program participants). (13) Telephone interview guide (for program dropouts). (14) In-person, in-depth interview guide (for program participants). (15) Telephone check-in guide (for program participants). (16) Semi-structured interview topic guide (for program staff). (17) Focus group discussion guide (for program participants). (18) Questionnaire (for program participants in focus groups). This 60-Day Federal Register Notice covers two new instruments: (19) Follow-up Survey (for RF study participants). (20) Follow-up Survey (for HM study participants). Respondents: Program applicants, program participants, program staff, and staff at referral agencies. Annual Burden Estimates Some burden has already been approved for this study, and the instruments are still in use. ANNUAL BURDEN—ALREADY APPROVED Evaluation component Total annual burden hours Site Selection ........................ Impact Study ......................... 50 4235 Total ............................... 4285 Some burden is currently under review, as of the date of this publication. ANNUAL BURDEN—CURRENTLY UNDER REVIEW Evaluation component Total annual burden hours Impact Study ......................... Implementation/Qualitative Study ................................. 8731 Total ............................... 8831 E:\FR\FM\28MYN1.SGM 28MYN1 1000 31943 Federal Register / Vol. 78, No. 102 / Tuesday, May 28, 2013 / Notices This current 60-Day Federal Register Notice covers two new instruments: ANNUAL BURDEN: CURRENT REQUEST Annual number of respondents Activity/respondent Average burden per response (hours) Number of responses per respondent Total annual burden hours IMPACT Responsible Fatherhood Grantee Impact Evaluation (19) Follow-up survey: Study participants ..................................................................................... 1,600 1 0.75 1,200 Healthy Marriage Grantee Impact Evaluation 1,600 1 0.75 1,200 Total ................................................................................................... mstockstill on DSK4VPTVN1PROD with NOTICES (20) RF study MIS: Study participants ..................................................................................... ........................ ........................ ........................ 2,400 Estimated Total Annual Burden Hours (for instruments previously approved and currently in use, instruments currently under review, and those associated with this 60-Day Notice): 15,516. In compliance with the requirements of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, the Administration for Children and Families is soliciting public comment on the specific aspects of the information collection described above. Copies of the proposed collection of information can be obtained and comments may be forwarded by writing to the Administration for Children and Families, Office of Planning, Research and Evaluation, 370 L’Enfant Promenade SW., Washington, DC 20447, Attn: OPRE Reports Clearance Officer. Email address: OPREinfocollection@acf.hhs.gov. All requests should be identified by the title of the information collection. The Department specifically requests comments on (a) whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information shall have practical utility; (b) the accuracy of the agency’s estimate of the burden of the proposed collection of information; (c) the quality, utility, and clarity of the information to be collected; and (d) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques or other forms of information technology. Consideration will be given to VerDate Mar<15>2010 17:46 May 24, 2013 Jkt 229001 comments and suggestions submitted within 60 days of this publication. Steven M. Hanmer, Reports Clearance Officer. [FR Doc. 2013–12588 Filed 5–24–13; 8:45 am] BILLING CODE 4184–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2013–D–0558] Draft Guidance for Industry on Contract Manufacturing Arrangements for Drugs: Quality Agreements; Availability AGENCY: Food and Drug Administration, HHS. ACTION: Notice. SUMMARY: The Food and Drug Administration (FDA) is announcing the availability of a draft guidance for industry entitled ‘‘Contract Manufacturing Arrangements for Drugs: Quality Agreements.’’ This guidance describes our current thinking on defining, establishing, and documenting the responsibilities of each party (or all parties) involved in the contract manufacturing of drugs subject to Current Good Manufacturing Practice (CGMP). In particular, we describe how parties involved in the contract manufacturing of drugs can utilize Quality Agreements to delineate their responsibilities and assure drug quality, safety, and efficacy. DATES: Although you can comment on any guidance at any time (see 21 CFR 10.115(g)(5)), to ensure that the Agency considers your comment on this draft PO 00000 Frm 00060 Fmt 4703 Sfmt 4703 guidance before it begins work on the final version of the guidance, submit either electronic or written comments on the draft guidance by July 29, 2013. ADDRESSES: Submit written requests for single copies of the draft guidance to the Division of Drug Information, Center for Drug Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 51, Rm. 2201, Silver Spring, MD 20993–0002; or Office of Communication, Outreach and Development (HFM–40), Center for Biologics Evaluation and Research (CBER), Food and Drug Administration, 1401 Rockville Pike, suite 200N, Rockville, MD 20852–1448; or Communications Staff (HFV–12), Center for Veterinary Medicine (CVM), Food and Drug Administration, 7519 Standish Pl., Rockville, MD 20855. Send one selfaddressed adhesive label to assist that office in processing your requests. See the SUPPLEMENTARY INFORMATION section for electronic access to the draft guidance document. Submit electronic comments on the draft guidance to https:// www.regulations.gov. Submit written comments to the Division of Dockets Management (HFA–305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. FOR FURTHER INFORMATION CONTACT: Paula Katz, Center for Drug Evaluation and Research, Bldg. 51, Rm. 4314, Food and Drug Administration, 10903 New Hampshire Ave., Silver Spring, MD 20993, 301–796–6972; or Stephen Ripley, Center for Biologics Evaluation and Research (HFM–17), Food and Drug Administration, 1401 Rockville Pike, Suite 200N, Rockville, MD 20852–1448, 301–827–6210; or Jonathan Bray, Center for Veterinary Medicine (HFV–232), E:\FR\FM\28MYN1.SGM 28MYN1

Agencies

[Federal Register Volume 78, Number 102 (Tuesday, May 28, 2013)]
[Notices]
[Pages 31942-31943]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-12588]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Proposed Information Collection Activity; Comment Request

    Title: Parents and Children Together (PACT) Evaluation.
    OMB No.: 0970-0403.
    Description: The Office of Planning, Research, and Evaluation 
(OPRE), Administration for Children and Families (ACF), U.S. Department 
of Health and Human Services (HHS), is proposing data collection 
activity as part of the Parents and Children Together (PACT) 
Evaluation. The objective of the PACT evaluation is to document and 
provide initial assessment of selected Responsible Fatherhood and 
Healthy Marriage grant programs that were authorized under the 2010 
Claims Resolution Act. This information will be critical to informing 
decisions related to future investments in programming as well as the 
design and operation of such services.
    PACT is utilizing three major, interrelated evaluation strategies: 
Impact evaluation; implementation evaluation; and qualitative 
evaluation. To collect data for these strategies, four instruments have 
been approved to-date, and 14 new instruments are under review as of 
the publish date of this notice.
    Instruments approved to-date:
    (1) Selecting Study Grantees (discussions with program and partner 
organization staff)--APPROVED April 20, 2012.
    (2) Introductory Script (for RF program staff to discuss with 
program applicants)--APPROVED October 31, 2012.
    (3) Baseline Survey (for RF study participants)--APPROVED October 
31, 2012.
    (4) RF study Management Information System (MIS)--APPROVED October 
31, 2012.
    Instruments under review at publish date of this notice:
    (5) Introductory Script (for HM program staff to discuss with 
program applicants).
    (6) Baseline Survey (for HM study participants).
    (7) HM study Management Information System (MIS) (8) Semi-
structured interview topic guide (for program staff).
    (9) On-line survey (for program staff).
    (10) Telephone interview guide (for program staff at referral 
organizations).
    (11) On-line Working Alliance Inventory (for program staff and 
participants).
    (12) Focus group discussion guide (for program participants).
    (13) Telephone interview guide (for program dropouts).
    (14) In-person, in-depth interview guide (for program 
participants).
    (15) Telephone check-in guide (for program participants).
    (16) Semi-structured interview topic guide (for program staff).
    (17) Focus group discussion guide (for program participants).
    (18) Questionnaire (for program participants in focus groups).
    This 60-Day Federal Register Notice covers two new instruments:
    (19) Follow-up Survey (for RF study participants).
    (20) Follow-up Survey (for HM study participants).
    Respondents: Program applicants, program participants, program 
staff, and staff at referral agencies.

Annual Burden Estimates

    Some burden has already been approved for this study, and the 
instruments are still in use.

                     Annual Burden--Already Approved
------------------------------------------------------------------------
                                                           Total annual
                  Evaluation component                     burden hours
------------------------------------------------------------------------
Site Selection..........................................              50
Impact Study............................................            4235
                                                         ---------------
    Total...............................................            4285
------------------------------------------------------------------------

    Some burden is currently under review, as of the date of this 
publication.

                  Annual Burden--Currently Under Review
------------------------------------------------------------------------
                                                           Total annual
                  Evaluation component                     burden hours
------------------------------------------------------------------------
Impact Study............................................            8731
Implementation/Qualitative Study........................            1000
                                                         ---------------
    Total...............................................            8831
------------------------------------------------------------------------


[[Page 31943]]

    This current 60-Day Federal Register Notice covers two new 
instruments:

                                         Annual Burden: Current Request
----------------------------------------------------------------------------------------------------------------
                                                                                      Average
                                                  Annual  number     Number of      burden per     Total annual
               Activity/respondent                      of         responses per     response      burden hours
                                                    respondents     respondent        (hours)
----------------------------------------------------------------------------------------------------------------
                                                     IMPACT
----------------------------------------------------------------------------------------------------------------
                                Responsible Fatherhood Grantee Impact Evaluation
----------------------------------------------------------------------------------------------------------------
(19) Follow-up survey:
    Study participants..........................           1,600               1            0.75           1,200
----------------------------------------------------------------------------------------------------------------
                                   Healthy Marriage Grantee Impact Evaluation
----------------------------------------------------------------------------------------------------------------
(20) RF study MIS:
    Study participants..........................           1,600               1            0.75           1,200
                                                 ---------------------------------------------------------------
        Total...................................  ..............  ..............  ..............           2,400
----------------------------------------------------------------------------------------------------------------

    Estimated Total Annual Burden Hours (for instruments previously 
approved and currently in use, instruments currently under review, and 
those associated with this 60-Day Notice): 15,516.
    In compliance with the requirements of Section 3506(c)(2)(A) of the 
Paperwork Reduction Act of 1995, the Administration for Children and 
Families is soliciting public comment on the specific aspects of the 
information collection described above. Copies of the proposed 
collection of information can be obtained and comments may be forwarded 
by writing to the Administration for Children and Families, Office of 
Planning, Research and Evaluation, 370 L'Enfant Promenade SW., 
Washington, DC 20447, Attn: OPRE Reports Clearance Officer. Email 
address: OPREinfocollection@acf.hhs.gov. All requests should be 
identified by the title of the information collection.
    The Department specifically requests comments on (a) whether the 
proposed collection of information is necessary for the proper 
performance of the functions of the agency, including whether the 
information shall have practical utility; (b) the accuracy of the 
agency's estimate of the burden of the proposed collection of 
information; (c) the quality, utility, and clarity of the information 
to be collected; and (d) ways to minimize the burden of the collection 
of information on respondents, including through the use of automated 
collection techniques or other forms of information technology. 
Consideration will be given to comments and suggestions submitted 
within 60 days of this publication.

Steven M. Hanmer,
Reports Clearance Officer.
[FR Doc. 2013-12588 Filed 5-24-13; 8:45 am]
BILLING CODE 4184-01-P
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