82 FR 24136 - Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals

DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration

Federal Register Volume 82, Issue 100 (May 25, 2017)

Page Range		24136-24136
FR Document		2017-10711

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.

Federal Register, Volume 82 Issue 100 (Thursday, May 25, 2017)

[Federal Register Volume 82, Number 100 (Thursday, May 25, 2017)]
[Notices]
[Page 24136]
From the Federal Register Online  [www.thefederalregister.org]
[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, 
[email protected].

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 http://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

24136 Federal Register / Vol. 82, No. 100 / Thursday, May 25, 2017 / Notices

Dated: May 18, 2017. ACTION: Notice. statements for the information
Anna K. Abram, collections are available on the Internet
Deputy Commissioner for Policy, Planning,
SUMMARY: The Food and Drug at http://www.reginfo.gov/public/do/
Legislation, and Analysis. Administration (FDA) is publishing a
PRAMain. An Agency may not conduct
list of information collections that have
[FR Doc. 2017–10710 Filed 5–24–17; 8:45 am] or sponsor, and a person is not required
been approved by the Office of
BILLING CODE 4164–01–P
Management and Budget (OMB) under to respond to, a collection of
the Paperwork Reduction Act of 1995. information unless it displays a
FOR FURTHER INFORMATION CONTACT: Ila
currently valid OMB control number.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES S. Mizrachi, FDA PRA Staff, Office of
Operations, Food and Drug
Food and Drug Administration Administration, Three White Flint
[Docket Nos. FDA–2013–N–1423; FDA–
North, 11601 Landsdown St., North
2013–N–0730; FDA–2012–N–0977; FDA– Bethesda, MD 20852, 301–796–7726,
2013–N–0557; FDA–2009–N–0380; FDA– PRAStaff@fda.hhs.gov.
2013–N–0514; FDA–2013–N–0190; FDA– SUPPLEMENTARY INFORMATION: The
2010–D–0350; FDA–2016–N–0538; FDA– following is a list of FDA information
2013–N–1428] collections recently approved by OMB
under section 3507 of the Paperwork
Agency Information Collection
Reduction Act of 1995 (44 U.S.C. 3507).
Activities; Announcement of Office of
The OMB control number and
Management and Budget Approvals
expiration date of OMB approval for
AGENCY: Food and Drug Administration, each information collection are shown
HHS. in table 1. Copies of the supporting

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 Used in Food-Contact Articles ............................................................... 0910–0298 12/31/2019
Regulations Restricting the Sale and Distribution of Cigarettes and Smokeless Tobacco to Protect Children
and Adolescents ................................................................................................................................................... 0910–0312 12/31/2019
Postmarket Surveillance of Medical Devices .......................................................................................................... 0910–0449 12/31/2019
Product Jurisdiction: Assignment of Agency Component for Review of Premarket Applications .......................... 0910–0523 12/31/2019
Administrative Procedures for Clinical laboratory Improvement Amendments of 1988 Categorization (42 CFR
493.17) ................................................................................................................................................................. 0910–0607 12/31/2019
Requirements under the Comprehensive Smokeless Tobacco Health Education Act of 1986; as amended by
the Family Smoking Prevention and Tobacco Control Act .................................................................................. 0910–0671 12/31/2019
Guidance for Industry on Tobacco Retailer Training Programs ............................................................................. 0910–0745 12/31/2019
Animation in Direct-to-Consumer Advertising ......................................................................................................... 0910–0826 12/31/2019
Guidance for Industry: Electronic Drug Product Reporting for Human Drug Compounding Outsourcing Facilities
Under Section 503B of the Federal Food, Drug, and Cosmetic Act ................................................................... 0910–0827 12/31/2019

Dated: May 18, 2017. 29, 2017. The BSC will provide input to Information about the meeting and
Anna K. Abram, the NTP on programmatic activities and registration is available at http://
Deputy Commissioner for Policy, Planning, issues. The preliminary agenda has been ntp.niehs.nih.gov/go/165.
Legislation, and Analysis. updated and topics include reports from
the NIEHS/NTP Director and NTP DATES: Meeting: June 29, 2017; it begins
[FR Doc. 2017–10711 Filed 5–24–17; 8:45 am]
Associate Director, and presentations on at 8:30 a.m. Eastern Standard Time
BILLING CODE 4164–01–P
programmatic activities including NTP (EST) until adjournment.
efforts and challenges toward studying Dated: May 11, 2017.
DEPARTMENT OF HEALTH AND real world exposures and a state of the John R. Bucher,
HUMAN SERVICES science evaluation of transgenerational Associate Director, National Toxicology
inheritance of health effects. This Program.
National Institutes of Health meeting will also provide opportunity [FR Doc. 2017–10695 Filed 5–24–17; 8:45 am]
for input on an effort being coordinated
National Toxicology Program Board of BILLING CODE 4140–01–P
by the Interagency Coordinating
Scientific Counselors; Announcement
Committee on the Validation of
of Meeting; Request for Comments;
Alternative Methods (ICCVAM) to
Amended Notice
explore new approaches for evaluating
SUMMARY: This notice amends Federal the safety of chemicals and medical
Register notice 82 FR 20484, published products in the United States. All other
May 2, 2017, announcing the National information in the original notice has
Toxicology Program (NTP) Board of not changed. Interested individuals
Scientific Counselors (BSC) meeting and should visit the meeting Web page to
requesting comments. The deadline for stay abreast of agenda topics and other
registration has been changed to June arrangements for the meeting.

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Document Created: 2018-11-08 08:52:45
Document Modified: 2018-11-08 08:52:45

Category		Regulatory Information
Collection		Federal Register
sudoc Class		AE 2.7: GS 4.107: AE 2.106:
Publisher		Office of the Federal Register, National Archives and Records Administration
Section		Notices
Action		Notice.
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, [email protected]
FR Citation		82 FR 24136

82 FR 24136 - Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals

DEPARTMENT OF HEALTH AND HUMAN SERVICESFood and Drug Administration

Federal Register Volume 82, Issue 100 (May 25, 2017)

DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration