Draft Current Intelligence Bulletin: The Occupational Exposure Banding Process: Guidance for the Evaluation of Chemical Hazards; Reopening of Comment Period, 28320-28321 [2017-12942]
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Federal Register / Vol. 82, No. 118 / Wednesday, June 21, 2017 / Notices
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Interested parties may submit comments
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Agreement No.: 011284–077.
Title: Ocean Carrier Equipment
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Rachel E. Dickon,
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Yao-Chin Chao,
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[FR Doc. 2017–12946 Filed 6–20–17; 8:45 am]
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[CDC–2017–0028, Docket Number NIOSH–
290]
Draft Current Intelligence Bulletin: The
Occupational Exposure Banding
Process: Guidance for the Evaluation
of Chemical Hazards; Reopening of
Comment Period
National Institute for
Occupational Safety and Health
(NIOSH) of the Centers for Disease
Control and Prevention (CDC),
Department of Health and Human
Services (HHS).
ACTION: Notice and reopening of
comment period.
AGENCY:
On March 15, 2017 the
National Institute for Occupational
Safety and Health (NIOSH) of the
Centers for Disease Control and
Prevention (CDC), published a notice in
the Federal Register [82 FR 13809]
announcing the availability of a draft
Current Intelligence Bulletin entitled
The Occupational Exposure Banding
Process: Guidance for the Evaluation of
Chemical Hazards for public comment.
NIOSH convened a public meeting in
Cincinnati, Ohio on Tuesday, May 23,
2017 to discuss the document. The draft
document can be found at
www.regulations.gov. by entering CDC–
2017–0028 in the search field and
clicking ‘‘Search.’’ Written comments
were to be received by June 13, 2017. In
response to a request from an interested
party, NIOSH is announcing the
reopening of the comment period.
DATES: Electronic or written comments
must be received by July 21, 2017.
FOR FURTHER INFORMATION CONTACT:
Melissa Seaton, NIOSH, Education and
Information Division, 1090 Tusculum
Avenue, MS C–32, Cincinnati, OH
45226, telephone (513) 533–8248, Fax
(513) 533–8230 (not toll free numbers),
email MSeaton@cdc.gov.
SUMMARY:
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Federal Register / Vol. 82, No. 118 / Wednesday, June 21, 2017 / Notices
You may submit comments,
identified by CDC–2017–0028 and
Docket Number NIOSH–290, by either
of the following two methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: National Institute for
Occupational Safety and Health, NIOSH
Docket Office, 1090 Tusculum Avenue,
MS C–34, Cincinnati, Ohio 45226–1998.
ADDRESSES:
John Howard,
Director, National Institute for Occupational
Safety and Health, Centers for Disease Control
and Prevention.
[FR Doc. 2017–12942 Filed 6–20–17; 8:45 am]
BILLING CODE 4163–19–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2017–N–2769]
Development of New Tuberculosis
Treatment Regimens—Scientific and
Clinical Trial Design Considerations;
Public Workshop; Request for
Comments
AGENCY:
Food and Drug Administration,
HHS.
Notice of public workshop;
request for comments.
ACTION:
The Food and Drug
Administration (FDA, the Agency, or
we) is/are announcing a public
workshop regarding scientific and
clinical trial design considerations for
the development of new tuberculosis
(TB) treatment regimens. This public
workshop is intended to provide
information for and gain perspective
from health care providers, other U.S.
Government Agencies, academic
experts, industry, and other
stakeholders regarding scientific and
clinical trial design considerations
related to the development of new TB
regimens.
SUMMARY:
The public workshop will be
held on July 19, 2017, from 8:30 a.m. to
5 p.m. Submit either electronic or
written comments on this public
workshop by August 1, 2017. See the
SUPPLEMENTARY INFORMATION section for
registration date and information. The
workshop draft agenda will be made
available at https://www.fda.gov/Drugs/
NewsEvents/ucm548365.htm prior to
the meeting.
ADDRESSES: The public workshop will
be held at FDA’s White Oak Campus,
10903 New Hampshire Ave., Building
31 Conference Center, the Great Room
(Rm. 1503), Silver Spring, MD 20993.
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DATES:
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Entrance for the public workshop
participants (non-FDA employees) is
through Building 1 where routine
security check procedures will be
performed. For parking and security
information, please refer to https://
www.fda.gov/AboutFDA/
WorkingatFDA/BuildingsandFacilities/
WhiteOakCampusInformation/
ucm241740.htm.
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 August 1, 2017. The https://
www.regulations.gov electronic filing
system will accept comments until
midnight eastern time on August 1,
2017. 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
as a manufacturing process. Please note
that if you include your name, contact
information, or other information that
identifies you in the body of your
comments, that information will be
posted on https://www.regulations.gov.
• If you want to submit a comment
with confidential information that you
do not wish to be made available to the
public, submit the comment as a
written/paper submission and in the
manner detailed (see ‘‘Written/Paper
Submissions’’ and ‘‘Instructions’’).
Written/Paper Submissions
Submit written/paper submissions as
follows:
• Mail/Hand delivery/Courier (for
written/paper submissions): Dockets
Management Staff (HFA–305), Food and
Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Dockets Management
Staff, FDA will post your comment, as
well as any attachments, except for
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information submitted, marked and
identified, as confidential, if submitted
as detailed in ‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2017–N–2769 for ‘‘Development of New
Tuberculosis Treatment Regimens—
Scientific and Clinical Trial Design
Considerations; Public Workshop;
Request for Comments.’’ Received
comments, those filed in a timely
manner (see ADDRESSES), will be placed
in the docket and, except for those
submitted as ‘‘Confidential
Submissions,’’ publicly viewable at
https://www.regulations.gov or at the
Dockets Management Staff between 9
a.m. and 4 p.m., Monday through
Friday.
• Confidential Submissions—To
submit a comment with confidential
information that you do not wish to be
made publicly available, submit your
comments only as a written/paper
submission. You should submit two
copies total. One copy will include the
information you claim to be confidential
with a heading or cover note that states
‘‘THIS DOCUMENT CONTAINS
CONFIDENTIAL INFORMATION.’’ The
Agency will review this copy, including
the claimed confidential information, in
its consideration of comments. The
second copy, which will have the
claimed confidential information
redacted/blacked out, will be available
for public viewing and posted on
https://www.regulations.gov. Submit
both copies to the Dockets Management
Staff. If you do not wish your name and
contact information to be made publicly
available, you can provide this
information on the cover sheet and not
in the body of your comments and you
must identify this information as
‘‘confidential.’’ Any information marked
as ‘‘confidential’’ will not be disclosed
except in accordance with 21 CFR 10.20
and other applicable disclosure law. For
more information about FDA’s posting
of comments to public dockets, see 80
FR 56469, September 18, 2015, or access
the information at: https://www.gpo.gov/
fdsys/pkg/FR-2015-09-18/pdf/201523389.pdf.
Docket: For access to the docket to
read background documents or the
electronic and written/paper comments
received, go to https://
www.regulations.gov and insert the
docket number, found in brackets in the
heading of this document, into the
‘‘Search’’ box and follow the prompts
and/or go to the Dockets Management
Staff, 5630 Fishers Lane, Rm. 1061,
Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT: Lori
Benner and/or Jessica Barnes, Center for
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Agencies
[Federal Register Volume 82, Number 118 (Wednesday, June 21, 2017)]
[Notices]
[Pages 28320-28321]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-12942]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[CDC-2017-0028, Docket Number NIOSH-290]
Draft Current Intelligence Bulletin: The Occupational Exposure
Banding Process: Guidance for the Evaluation of Chemical Hazards;
Reopening of Comment Period
AGENCY: National Institute for Occupational Safety and Health (NIOSH)
of the Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice and reopening of comment period.
-----------------------------------------------------------------------
SUMMARY: On March 15, 2017 the National Institute for Occupational
Safety and Health (NIOSH) of the Centers for Disease Control and
Prevention (CDC), published a notice in the Federal Register [82 FR
13809] announcing the availability of a draft Current Intelligence
Bulletin entitled The Occupational Exposure Banding Process: Guidance
for the Evaluation of Chemical Hazards for public comment. NIOSH
convened a public meeting in Cincinnati, Ohio on Tuesday, May 23, 2017
to discuss the document. The draft document can be found at
www.regulations.gov. by entering CDC-2017-0028 in the search field and
clicking ``Search.'' Written comments were to be received by June 13,
2017. In response to a request from an interested party, NIOSH is
announcing the reopening of the comment period.
DATES: Electronic or written comments must be received by July 21,
2017.
FOR FURTHER INFORMATION CONTACT: Melissa Seaton, NIOSH, Education and
Information Division, 1090 Tusculum Avenue, MS C-32, Cincinnati, OH
45226, telephone (513) 533-8248, Fax (513) 533-8230 (not toll free
numbers), email MSeaton@cdc.gov.
[[Page 28321]]
ADDRESSES: You may submit comments, identified by CDC-2017-0028 and
Docket Number NIOSH-290, by either of the following two methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the instructions for submitting comments.
Mail: National Institute for Occupational Safety and
Health, NIOSH Docket Office, 1090 Tusculum Avenue, MS C-34, Cincinnati,
Ohio 45226-1998.
John Howard,
Director, National Institute for Occupational Safety and Health,
Centers for Disease Control and Prevention.
[FR Doc. 2017-12942 Filed 6-20-17; 8:45 am]
BILLING CODE 4163-19-P