National Toxicology Program Board of Scientific Counselors; Announcement of Meeting; Request for Comments; Amended Notice, 24136 [2017-10695]
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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
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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]
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[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: 2017-10695]
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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
SUMMARY: 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 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.
Information about the meeting and registration is available at https://ntp.niehs.nih.gov/go/165.
DATES: Meeting: June 29, 2017; it begins at 8:30 a.m. Eastern Standard
Time (EST) until adjournment.
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
