Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals, 24136 [2017-10711]

Download as PDF 24136 Federal Register / Vol. 82, No. 100 / Thursday, May 25, 2017 / Notices Dated: May 18, 2017. Anna K. Abram, Deputy Commissioner for Policy, Planning, Legislation, and Analysis. ACTION: 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, FDA PRA Staff, Office of Operations, Food and Drug Administration, Three White Flint North, 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 SUMMARY: [FR Doc. 2017–10710 Filed 5–24–17; 8:45 am] BILLING CODE 4164–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket Nos. FDA–2013–N–1423; FDA– 2013–N–0730; FDA–2012–N–0977; FDA– 2013–N–0557; FDA–2009–N–0380; FDA– 2013–N–0514; FDA–2013–N–0190; FDA– 2010–D–0350; FDA–2016–N–0538; FDA– 2013–N–1428] Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals AGENCY: Notice. Food and Drug Administration, HHS. 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 OMB control No. Title of collection Importer’s Entry Notice ............................................................................................................................................ Threshold of Regulation for Substances Used in Food-Contact Articles ............................................................... Regulations Restricting the Sale and Distribution of Cigarettes and Smokeless Tobacco to Protect Children and Adolescents ................................................................................................................................................... Postmarket Surveillance of Medical Devices .......................................................................................................... Product Jurisdiction: Assignment of Agency Component for Review of Premarket Applications .......................... Administrative Procedures for Clinical laboratory Improvement Amendments of 1988 Categorization (42 CFR 493.17) ................................................................................................................................................................. Requirements under the Comprehensive Smokeless Tobacco Health Education Act of 1986; as amended by the Family Smoking Prevention and Tobacco Control Act .................................................................................. Guidance for Industry on Tobacco Retailer Training Programs ............................................................................. Animation in Direct-to-Consumer Advertising ......................................................................................................... Guidance for Industry: Electronic Drug Product Reporting for Human Drug Compounding Outsourcing Facilities Under Section 503B of the Federal Food, Drug, and Cosmetic Act ................................................................... Dated: May 18, 2017. Anna K. Abram, Deputy Commissioner for Policy, Planning, Legislation, and Analysis. [FR Doc. 2017–10711 Filed 5–24–17; 8:45 am] BILLING CODE 4164–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Toxicology Program Board of Scientific Counselors; Announcement of Meeting; Request for Comments; Amended Notice This notice amends Federal Register notice 82 FR 20484, published May 2, 2017, announcing the National Toxicology Program (NTP) Board of Scientific Counselors (BSC) meeting and requesting comments. The deadline for registration has been changed to June SUMMARY: VerDate Sep<11>2014 18:04 May 24, 2017 Jkt 241001 29, 2017. The BSC will provide input to the NTP on programmatic activities and issues. The preliminary agenda has been updated and topics include reports from the NIEHS/NTP Director and NTP Associate Director, and presentations on programmatic activities including NTP efforts and challenges toward studying real world exposures and a state of the science evaluation of transgenerational inheritance of health effects. This meeting will also provide opportunity for input on an effort being coordinated by the Interagency Coordinating Committee on the Validation of Alternative Methods (ICCVAM) to explore new approaches for evaluating the safety of chemicals and medical products in the United States. All other information in the original notice has not changed. Interested individuals should visit the meeting Web page to stay abreast of agenda topics and other arrangements for the meeting. PO 00000 Frm 00042 Fmt 4703 Sfmt 9990 Date approval expires 0910–0046 0910–0298 12/31/2019 12/31/2019 0910–0312 0910–0449 0910–0523 12/31/2019 12/31/2019 12/31/2019 0910–0607 12/31/2019 0910–0671 0910–0745 0910–0826 12/31/2019 12/31/2019 12/31/2019 0910–0827 12/31/2019 Information about the meeting and registration is available at https:// ntp.niehs.nih.gov/go/165. Meeting: June 29, 2017; it begins at 8:30 a.m. Eastern Standard Time (EST) until adjournment. DATES: Dated: May 11, 2017. John R. Bucher, Associate Director, National Toxicology Program. [FR Doc. 2017–10695 Filed 5–24–17; 8:45 am] BILLING CODE 4140–01–P E:\FR\FM\25MYN1.SGM 25MYN1

Agencies

[Federal Register Volume 82, Number 100 (Thursday, May 25, 2017)]
[Notices]
[Page 24136]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-10711]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket Nos. FDA-2013-N-1423; FDA-2013-N-0730; FDA-2012-N-0977; FDA-
2013-N-0557; FDA-2009-N-0380; FDA-2013-N-0514; FDA-2013-N-0190; FDA-
2010-D-0350; FDA-2016-N-0538; FDA-2013-N-1428]


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

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

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

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, FDA PRA Staff, Office 
of Operations, Food and Drug Administration, Three White Flint North, 
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
------------------------------------------------------------------------
                                            OMB control    Date approval
           Title of collection                  No.           expires
------------------------------------------------------------------------
Importer's Entry Notice.................       0910-0046      12/31/2019
Threshold of Regulation for Substances         0910-0298      12/31/2019
 Used in Food-Contact Articles..........
Regulations Restricting the Sale and           0910-0312      12/31/2019
 Distribution of Cigarettes and
 Smokeless Tobacco to Protect Children
 and Adolescents........................
Postmarket Surveillance of Medical             0910-0449      12/31/2019
 Devices................................
Product Jurisdiction: Assignment of            0910-0523      12/31/2019
 Agency Component for Review of
 Premarket Applications.................
Administrative Procedures for Clinical         0910-0607      12/31/2019
 laboratory Improvement Amendments of
 1988 Categorization (42 CFR 493.17)....
Requirements under the Comprehensive           0910-0671      12/31/2019
 Smokeless Tobacco Health Education Act
 of 1986; as amended by the Family
 Smoking Prevention and Tobacco Control
 Act....................................
Guidance for Industry on Tobacco               0910-0745      12/31/2019
 Retailer Training Programs.............
Animation in Direct-to-Consumer                0910-0826      12/31/2019
 Advertising............................
Guidance for Industry: Electronic Drug         0910-0827      12/31/2019
 Product Reporting for Human Drug
 Compounding Outsourcing Facilities
 Under Section 503B of the Federal Food,
 Drug, and Cosmetic Act.................
------------------------------------------------------------------------


    Dated: May 18, 2017.
Anna K. Abram,
Deputy Commissioner for Policy, Planning, Legislation, and Analysis.
[FR Doc. 2017-10711 Filed 5-24-17; 8:45 am]
BILLING CODE 4164-01-P
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