Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals, 56031 [2017-25452]

Download as PDF 56031 Federal Register / Vol. 82, No. 226 / Monday, November 27, 2017 / Notices Estimated Total/Annual Burden Hours: 244. 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, 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. Mary Jones, ACF/OPRE Certifying Officer. [FR Doc. 2017–25444 Filed 11–24–17; 8:45 am] BILLING CODE 4184–37–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket Nos. FDA–2010–N–0601, FDA– 2010–N–0598, FDA–2010–N–0600, FDA– 2007–N–0037, FDA–2010–N–0597, FDA– 2011–N–0017, and FDA–2016–N–2496] Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals AGENCY: Food and Drug Administration, HHS. ACTION: Notice. The Food and Drug Administration (FDA) is publishing a list of information collections that have SUMMARY: been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995. FOR FURTHER INFORMATION CONTACT: Ila S. Mizrachi, Office of Operations, Food and Drug Administration, Three White Flint North, 10A–12M, 11601 Landsdown St., North Bethesda, MD 20852, 301–796–7726, PRAStaff@ fda.hhs.gov. The following is a list of FDA information collections recently approved by OMB under section 3507 of the Paperwork Reduction Act of 1995 (44 U.S.C. 3507). The OMB control number and expiration date of OMB approval for each information collection are shown in Table 1. Copies of the supporting statements for the information collections are available on the internet at https://www.reginfo.gov/public/do/ PRAMain. An Agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. SUPPLEMENTARY INFORMATION: TABLE 1—LIST OF INFORMATION COLLECTIONS APPROVED BY OMB OMB control No. Title of collection Current Good Manufacturing Practice for Medicated Feeds ...................................................................... Current Good Manufacturing Practice for Type A Medicated Articles ........................................................ Animal Drug User Fee Cover Sheet, Form FDA 3546 ............................................................................... Animal Drug User Fee Waivers and Reductions ........................................................................................ Index of Legally Marketed Unappropriated New Animal Drugs for Minor Species .................................... Voluntary National Retail Food Regulatory Program Standards ................................................................ Impact Trade Auxiliary Communication System ......................................................................................... Dated: November 20, 2017. Leslie Kux, Associate Commissioner for Policy. [FR Doc. 2017–25452 Filed 11–24–17; 8:45 am] BILLING CODE 4164–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration asabaliauskas on DSKBBXCHB2PROD with NOTICES [Docket No. FDA–2010–N–0161] Agency Information Collection Activities; Proposed Collection; Comment Request; Export of Food and Drug Administration-Regulated Products: Export Certificates AGENCY: Food and Drug Administration, HHS. ACTION: Notice. The Food and Drug Administration (FDA or Agency) is announcing an opportunity for public SUMMARY: VerDate Sep<11>2014 16:59 Nov 24, 2017 Jkt 244001 comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of 1995 (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 export certificates for the export of FDA-regulated products. Submit either electronic or written comments on the collection of information by January 26, 2018. ADDRESSES: You may submit comments as follows. Please note that late, untimely filed comments will not be considered. Electronic comments must be submitted on or before January 26, 2018. The https://www.regulations.gov electronic filing system will accept comments until midnight Eastern Time DATES: PO 00000 Frm 00047 Fmt 4703 Sfmt 4703 0910–0152 0910–0154 0910–0539 0910–0540 0910–0620 0910–0621 0910–0842 Date approval expires 8/31/2020 8/31/2020 8/31/2020 8/31/2020 8/31/2020 8/31/2020 8/31/2020 at the end of January 26, 2018. Comments received by mail/hand delivery/courier (for written/paper submissions) will be considered timely if they are postmarked or the delivery service acceptance receipt is on or before that date. Electronic Submissions Submit electronic comments in the following way: • Federal eRulemaking Portal: https://www.regulations.gov. Follow the instructions for submitting comments. Comments submitted electronically, including attachments, to https:// 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 E:\FR\FM\27NON1.SGM 27NON1

Agencies

[Federal Register Volume 82, Number 226 (Monday, November 27, 2017)]
[Notices]
[Page 56031]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-25452]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket Nos. FDA-2010-N-0601, FDA-2010-N-0598, FDA-2010-N-0600, FDA-
2007-N-0037, FDA-2010-N-0597, FDA-2011-N-0017, and FDA-2016-N-2496]


Agency Information Collection Activities; Announcement of Office 
of Management and Budget Approvals

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

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SUMMARY: The Food and Drug Administration (FDA) is publishing a list of 
information collections that have been approved by the Office of 
Management and Budget (OMB) under the Paperwork Reduction Act of 1995.

FOR FURTHER INFORMATION CONTACT: Ila S. Mizrachi, Office of Operations, 
Food and Drug Administration, Three White Flint North, 10A-12M, 11601 
Landsdown St., North Bethesda, MD 20852, 301-796-7726, 
PRAStaff@fda.hhs.gov.

SUPPLEMENTARY INFORMATION: The following is a list of FDA information 
collections recently approved by OMB under section 3507 of the 
Paperwork Reduction Act of 1995 (44 U.S.C. 3507). The OMB control 
number and expiration date of OMB approval for each information 
collection are shown in Table 1. Copies of the supporting statements 
for the information collections are available on the internet at 
https://www.reginfo.gov/public/do/PRAMain. An Agency may not conduct or 
sponsor, and a person is not required to respond to, a collection of 
information unless it displays a currently valid OMB control number.

        Table 1--List of Information Collections Approved by OMB
------------------------------------------------------------------------
                                                         Date  approval
        Title of collection          OMB  control No.       expires
------------------------------------------------------------------------
Current Good Manufacturing                  0910-0152          8/31/2020
 Practice for Medicated Feeds.....
Current Good Manufacturing                  0910-0154          8/31/2020
 Practice for Type A Medicated
 Articles.........................
Animal Drug User Fee Cover Sheet,           0910-0539          8/31/2020
 Form FDA 3546....................
Animal Drug User Fee Waivers and            0910-0540          8/31/2020
 Reductions.......................
Index of Legally Marketed                   0910-0620          8/31/2020
 Unappropriated New Animal Drugs
 for Minor Species................
Voluntary National Retail Food              0910-0621          8/31/2020
 Regulatory Program Standards.....
Impact Trade Auxiliary                      0910-0842          8/31/2020
 Communication System.............
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    Dated: November 20, 2017.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2017-25452 Filed 11-24-17; 8:45 am]
 BILLING CODE 4164-01-P