Draft Criteria for a Recommended Standard: Occupational Exposure to 1-Bromopropane (1-BP); Notice of Public Meeting; Availability of Draft Document for Comment, 7122-7123 [2016-02650]
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Federal Register / Vol. 81, No. 27 / Wednesday, February 10, 2016 / Notices
Model EBA 75 CCER for Mining.
Pursuant to 42 CFR 84.301,
manufacturers may continue to
manufacture, label, and sell largecapacity CCERs approved under the
former regulatory standard in subpart H
(those CCERs with a rated service time
of greater than 50 minutes) for mining,
until 1 year after this approval date, or
until January 4, 2017.
All types of CCERs approved under
subpart H that were manufactured and
labeled as NIOSH-approved and sold by
April 9, 2015, as well as those units
manufactured and labeled as NIOSHapproved and sold during the extended
time periods pursuant to § 84.301, may
continue to be used as NIOSH-approved
respirators until the end of their service
life.
Dated: February 1, 2016.
John Howard,
Director, National Institute for Occupational
Safety and Health, Centers for Disease Control
and Prevention.
[FR Doc. 2016–02649 Filed 2–9–16; 8:45 am]
BILLING CODE 4163–19–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[Docket Number CDC–2016–0003; NIOSH
057–A]
Draft Criteria for a Recommended
Standard: Occupational Exposure to 1Bromopropane (1–BP); Notice of
Public Meeting; Availability of Draft
Document for Comment
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 of public meeting and
availability of draft document for public
comment.
AGENCY:
On September 16, 2009, the
National Institute for Occupational
Safety and Health (NIOSH), Centers for
Disease Control and Prevention (CDC)
announced in the Federal Register
https://www.gpo.gov/fdsys/pkg/FR2009-09-16/pdf/E9-22297.pdf plans to
evaluate the scientific data on
1-bromopropane (1–BP) and to issue its
findings on the potential health risks. A
draft document entitled, Criteria for a
Recommended Standard: Occupational
Exposure to 1-Bromopropane (1–BP),
has been developed which contains an
assessment of toxicological data and
provides recommendations for the safe
asabaliauskas on DSK9F6TC42PROD with NOTICES2
SUMMARY:
VerDate Sep<11>2014
17:22 Feb 09, 2016
Jkt 238001
handling of 1–BP-containing materials.
NIOSH is seeking comments on the draft
document and plans to have a public
meeting to discuss the document. The
draft document and instructions for
submitting comments can be found at
www.regulations.gov.
DATES: The public meeting will be held
on March 30, 2016, 9:00 a.m.–3:00 p.m.
Eastern Time, or after the last public
commenter has spoken, whichever
occurs first. Comments must be received
by April 29, 2016.
ADDRESSES: The public meeting will be
held at the NIOSH/CDC Robert A. Taft
Laboratories, Auditorium, 1150
Tusculum Avenue, Cincinnati, Ohio
45226.
FOR FURTHER INFORMATION CONTACT: G.
Scott Dotson, NIOSH, Education and
Information Division, Robert A. Taft
Laboratories, 1090 Tusculum Avenue,
Cincinnati, OH 45226, (513) 533–8540
(not a toll free number).
SUPPLEMENTARY INFORMATION:
I. Background
On September 16, 2009, the National
Institute for Occupational Safety and
Health (NIOSH), Centers for Disease
Control and Prevention (CDC)
announced in the Federal Register
plans to evaluate the scientific data on
1-bromopropane (1–BP) and to issue its
findings on the potential health risks.
The results of this evaluation are
presented in the draft document,
Criteria for a Recommended Standard:
Occupational Exposure to
1-Bromopropane (1–BP). The purpose of
the public meeting and public comment
period is to obtain comments on the
draft document. Special emphasis will
be placed on the following:
• Whether the health hazard
identification, risk estimation, and
discussion of health effects of 1–BP are
a reasonable reflection of the current
understanding of the scientific
literature;
• Identifying workplaces and
occupations where exposure to 1–BP
may occur;
• Identifying studies on health effects
associated with occupational exposure
to 1–BP that were not identified in the
draft;
• Identifying current strategies for
controlling or preventing exposure to 1–
BP (e.g., engineering controls, work
practices, personal protective
equipment);
• Identifying current exposure
measurement methods and challenges
in measuring workplace exposures to 1–
BP; and
• Identifying areas for future
collaborative efforts (e.g., research,
PO 00000
Frm 00059
Fmt 4703
Sfmt 4703
communication, development of
exposure measurement and control
strategies).
As part of the review of this draft
criteria document, reviewers are asked
to address the following critical
questions:
(1) Does the draft criteria document
accurately identify and characterize the
health hazards of occupational
exposures to 1–BP based on the current
understanding of the scientific
literature? Please identify any additional
relevant literature that NIOSH should
consider when developing its
recommendations. Is the risk estimation
for 1–BP presented in the draft criteria
document a reasonable reflection of the
current understanding of the scientific
literature? Please describe any changes
in the risk estimation that NIOSH
should consider and provide supporting
scientific literature.
(2) Are there other risk assessment
methods or health endpoints that
NIOSH should consider for estimating
risks of 1–BP? Please provide
supporting scientific literature or other
evidence to support your
recommendations.
(3) In this draft criteria document,
NIOSH proposes a recommended
exposure limit (REL) to prevent a risk of
one excess cancer in 1000 workers
exposed to 1–BP for a 45-year working
lifetime. During development of the
draft criteria document, NIOSH also
considered setting the REL at a level to
prevent 1 excess cancer in 10,000
workers for a 45-year working lifetime.
Please comment on the excess cancer
risk level and resulting REL for 1–BP.
(4) Is the relationship between
exposure to 1–BP and biological activity
(toxicity) accurately presented in the
draft criteria document?
(5) Are the recommended strategies
for controlling or preventing exposure to
1–BP (e.g., engineering controls, work
practices, personal protective
equipment) reasonable and technically
feasible?
(6) Are there other techniques or
technologies capable of controlling
workplace exposures to 1–BP that
should be discussed in the draft criteria
document?
(7) Are the exposure measurement
methods and the associated challenges
in measuring workplace exposures to 1–
BP adequately addressed in the draft
criteria document?
(8) Are there medical screening and
surveillance measures, such as specific
diagnostic tests, guidelines, and metrics,
that should be implemented for workers
expected of being exposed to 1–BP that
are not discussed in the draft criteria
document?
E:\FR\FM\10FEN1.SGM
10FEN1
Federal Register / Vol. 81, No. 27 / Wednesday, February 10, 2016 / Notices
asabaliauskas on DSK9F6TC42PROD with NOTICES2
(9) Are there biological indices or
metrics that should be used to aid in the
interpretation of biomonitoring data for
1–BP? What is the most appropriate
biomarker that can confirm and quantify
occupational exposures to 1–BP?
(10) Should acute exposure
recommendations, such as a short term
exposure limit (STEL), be derived for 1–
BP? If so, what data support the
development of the STEL?
(11) NIOSH provided Globally
Harmonized System (GHS) of
Classification and Labelling of
Chemicals designations for health
endpoints evaluated in the criteria
document. Please comment on the
utility of these classifications for hazard
communication. Are these
classifications helpful for employers?
II. Public Meeting
NIOSH will hold a public meeting on
the draft document Criteria for a
Recommended Standard: Occupational
Exposure to 1-Bromopropane (1–BP) to
allow commenters to provide oral
comments on the draft document, to
inform NIOSH about additional relevant
data or information, and to ask
questions on the draft document and
NIOSH recommendations.
This meeting is open to the public.
Attendance is limited only by the space
available. The meeting room
accommodates 100 people. The meeting
will be open to a limited number of
participants through a conference call
phone number and Webcast live on the
Internet.
Notification of intent to attend the
meeting, for in-person and remote
participation, must be made to the
NIOSH Docket Office, at nioshdocket@
cdc.gov, (513) 533–8611, no later than
March 16, 2016. Priority for attendance
will be given to those providing oral
comments. Other requests to attend the
meeting will then be accommodated on
a first-come, first-served basis.
Registration is required for in-person
attendance and remote participation.
Because this meeting is being held at a
federal site, pre-registration is required
on or before March 16, 2016 and a
government-issued photo ID (driver’s
license, military ID or passport) will be
required to obtain entrance to the
facility. There will be an airport-type
security check. Non-US citizens need to
register by February 24, 2016 to allow
sufficient time for mandatory facility
security clearance procedures to be
completed. This information will be
transmitted to the CDC Security Office
for approval. An email confirming
registration will be sent from NIOSH for
both in-person participation and audio
conferencing participation.
VerDate Sep<11>2014
17:22 Feb 09, 2016
Jkt 238001
Oral comments will be permitted for
15 minutes. If additional time becomes
available, presenters will be notified.
All requests to present should contain
the name, address, telephone number,
and relevant business affiliations of the
presenter, topic of the presentation,
whether you will be presenting in
person or by phone, and the
approximate time requested for the
presentation. An email confirming
registration will be sent from the NIOSH
Docket Office and will include details
needed to participate. Oral comments
given at the meeting will be recorded
and included in the docket.
After reviewing the requests for
presentations, NIOSH will notify the
presenter when his/her presentation is
scheduled. If a participant is not in
attendance when his/her presentation is
scheduled to begin, the remaining
participants will be heard in order. After
the last scheduled speaker is heard,
participants who missed their assigned
times may be allowed to speak, limited
by time available.
Attendees who wish to speak but did
not submit a request for the opportunity
to make a presentation may be given
this opportunity after the scheduled
speakers are heard, at the discretion of
the presiding officer and limited by time
available.
You may submit comments, identified
by CDC 2016–0003 and NIOSH 057–A,
by either of the following methods:
• Federal eRulemaking Portal:
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.
Instructions: All information received
in response to this notice must include
the agency name and docket number
[CDC–2016–0003; NIOSH 057–A]. All
relevant comments received will be
posted without change to
www.regulations.gov including any
personal information provided. All
information will be available for public
examination and copying at the NIOSH
Docket Office, 1150 Tusculum Avenue,
Room 155, Cincinnati, Ohio 45226.
Non-U.S. Citizens: Because of CDC
Security Regulations, any non-U.S.
citizen wishing to attend this meeting
must provide the following information
in writing to the NIOSH Docket Officer
at the address below no later than
February 24, 2016.
Name:
Gender:
Date of Birth:
Place of Birth (city, province, state, country):
Citizenship:
Passport Number:
PO 00000
Frm 00060
Fmt 4703
Sfmt 4703
7123
Date of Passport Issue:
Date of Passport Expiration:
Type of Visa:
U.S. Naturalization Number (if a naturalized
citizen):
U.S. Naturalization Date (if a naturalized
citizen):
Visitor’s Organization:
Organization Address:
Organization Telephone Number:
Visitor’s Position/Title within the
Organization:
This information will be transmitted
to the CDC Security Office for approval.
Visitors will be notified as soon as
approval has been obtained.
Public Review
The external review of the draft
document has been (1) developed in
accordance with Office of Management
and Budget (OMB) guidelines, (2) is
consistent with NIOSH peer review
practice, and (3) is meant to ensure that
credible and appropriate science is
reflected within the draft document.
Dated: February 4, 2016.
John Howard,
Director, National Institute for Occupational
Safety and Health, Centers for Disease Control
and Prevention.
[FR Doc. 2016–02650 Filed 2–9–16; 8:45 am]
BILLING CODE 4163–19–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Disease, Disability, and Injury
Prevention and Control Special
Emphasis Panel (SEP): Initial Review
In accordance with Section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), the Centers for Disease
Control and Prevention (CDC)
announces a meeting for the initial
review of applications in response to
Funding Opportunity Announcement
(FOA) DP16–004, Childhood Obesity
Research Demonstration 2.0.
Time and Date: 10:00 a.m.–6:00 p.m.,
EST, March 15–16, 2016 (Closed).
Place: Teleconference.
Status: The meeting will be closed to
the public in accordance with
provisions set forth in Section
552b(c)(4) and (6), Title 5 U.S.C., and
the determination of the Director,
Management Analysis and Services
Office, CDC, pursuant to Public Law 92–
463.
Matters for Discussion: The meeting
will include the initial review,
discussion, and evaluation of
applications received in response to
FOA DP16–004, Childhood Obesity
Research Demonstration 2.0.
E:\FR\FM\10FEN1.SGM
10FEN1
Agencies
[Federal Register Volume 81, Number 27 (Wednesday, February 10, 2016)]
[Notices]
[Pages 7122-7123]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-02650]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[Docket Number CDC-2016-0003; NIOSH 057-A]
Draft Criteria for a Recommended Standard: Occupational Exposure
to 1-Bromopropane (1-BP); Notice of Public Meeting; Availability of
Draft Document for Comment
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 of public meeting and availability of draft document for
public comment.
-----------------------------------------------------------------------
SUMMARY: On September 16, 2009, the National Institute for Occupational
Safety and Health (NIOSH), Centers for Disease Control and Prevention
(CDC) announced in the Federal Register https://www.gpo.gov/fdsys/pkg/FR-2009-09-16/pdf/E9-22297.pdf plans to evaluate the scientific data on
1-bromopropane (1-BP) and to issue its findings on the potential health
risks. A draft document entitled, Criteria for a Recommended Standard:
Occupational Exposure to 1-Bromopropane (1-BP), has been developed
which contains an assessment of toxicological data and provides
recommendations for the safe handling of 1-BP-containing materials.
NIOSH is seeking comments on the draft document and plans to have a
public meeting to discuss the document. The draft document and
instructions for submitting comments can be found at
www.regulations.gov.
DATES: The public meeting will be held on March 30, 2016, 9:00 a.m.-
3:00 p.m. Eastern Time, or after the last public commenter has spoken,
whichever occurs first. Comments must be received by April 29, 2016.
ADDRESSES: The public meeting will be held at the NIOSH/CDC Robert A.
Taft Laboratories, Auditorium, 1150 Tusculum Avenue, Cincinnati, Ohio
45226.
FOR FURTHER INFORMATION CONTACT: G. Scott Dotson, NIOSH, Education and
Information Division, Robert A. Taft Laboratories, 1090 Tusculum
Avenue, Cincinnati, OH 45226, (513) 533-8540 (not a toll free number).
SUPPLEMENTARY INFORMATION:
I. Background
On September 16, 2009, the National Institute for Occupational
Safety and Health (NIOSH), Centers for Disease Control and Prevention
(CDC) announced in the Federal Register plans to evaluate the
scientific data on 1-bromopropane (1-BP) and to issue its findings on
the potential health risks. The results of this evaluation are
presented in the draft document, Criteria for a Recommended Standard:
Occupational Exposure to 1-Bromopropane (1-BP). The purpose of the
public meeting and public comment period is to obtain comments on the
draft document. Special emphasis will be placed on the following:
Whether the health hazard identification, risk estimation,
and discussion of health effects of 1-BP are a reasonable reflection of
the current understanding of the scientific literature;
Identifying workplaces and occupations where exposure to
1-BP may occur;
Identifying studies on health effects associated with
occupational exposure to 1-BP that were not identified in the draft;
Identifying current strategies for controlling or
preventing exposure to 1-BP (e.g., engineering controls, work
practices, personal protective equipment);
Identifying current exposure measurement methods and
challenges in measuring workplace exposures to 1-BP; and
Identifying areas for future collaborative efforts (e.g.,
research, communication, development of exposure measurement and
control strategies).
As part of the review of this draft criteria document, reviewers
are asked to address the following critical questions:
(1) Does the draft criteria document accurately identify and
characterize the health hazards of occupational exposures to 1-BP based
on the current understanding of the scientific literature? Please
identify any additional relevant literature that NIOSH should consider
when developing its recommendations. Is the risk estimation for 1-BP
presented in the draft criteria document a reasonable reflection of the
current understanding of the scientific literature? Please describe any
changes in the risk estimation that NIOSH should consider and provide
supporting scientific literature.
(2) Are there other risk assessment methods or health endpoints
that NIOSH should consider for estimating risks of 1-BP? Please provide
supporting scientific literature or other evidence to support your
recommendations.
(3) In this draft criteria document, NIOSH proposes a recommended
exposure limit (REL) to prevent a risk of one excess cancer in 1000
workers exposed to 1-BP for a 45-year working lifetime. During
development of the draft criteria document, NIOSH also considered
setting the REL at a level to prevent 1 excess cancer in 10,000 workers
for a 45-year working lifetime. Please comment on the excess cancer
risk level and resulting REL for 1-BP.
(4) Is the relationship between exposure to 1-BP and biological
activity (toxicity) accurately presented in the draft criteria
document?
(5) Are the recommended strategies for controlling or preventing
exposure to 1-BP (e.g., engineering controls, work practices, personal
protective equipment) reasonable and technically feasible?
(6) Are there other techniques or technologies capable of
controlling workplace exposures to 1-BP that should be discussed in the
draft criteria document?
(7) Are the exposure measurement methods and the associated
challenges in measuring workplace exposures to 1-BP adequately
addressed in the draft criteria document?
(8) Are there medical screening and surveillance measures, such as
specific diagnostic tests, guidelines, and metrics, that should be
implemented for workers expected of being exposed to 1-BP that are not
discussed in the draft criteria document?
[[Page 7123]]
(9) Are there biological indices or metrics that should be used to
aid in the interpretation of biomonitoring data for 1-BP? What is the
most appropriate biomarker that can confirm and quantify occupational
exposures to 1-BP?
(10) Should acute exposure recommendations, such as a short term
exposure limit (STEL), be derived for 1-BP? If so, what data support
the development of the STEL?
(11) NIOSH provided Globally Harmonized System (GHS) of
Classification and Labelling of Chemicals designations for health
endpoints evaluated in the criteria document. Please comment on the
utility of these classifications for hazard communication. Are these
classifications helpful for employers?
II. Public Meeting
NIOSH will hold a public meeting on the draft document Criteria for
a Recommended Standard: Occupational Exposure to 1-Bromopropane (1-BP)
to allow commenters to provide oral comments on the draft document, to
inform NIOSH about additional relevant data or information, and to ask
questions on the draft document and NIOSH recommendations.
This meeting is open to the public. Attendance is limited only by
the space available. The meeting room accommodates 100 people. The
meeting will be open to a limited number of participants through a
conference call phone number and Webcast live on the Internet.
Notification of intent to attend the meeting, for in-person and
remote participation, must be made to the NIOSH Docket Office, at
nioshdocket@cdc.gov, (513) 533-8611, no later than March 16, 2016.
Priority for attendance will be given to those providing oral comments.
Other requests to attend the meeting will then be accommodated on a
first-come, first-served basis.
Registration is required for in-person attendance and remote
participation. Because this meeting is being held at a federal site,
pre-registration is required on or before March 16, 2016 and a
government-issued photo ID (driver's license, military ID or passport)
will be required to obtain entrance to the facility. There will be an
airport-type security check. Non[hyphen]US citizens need to register by
February 24, 2016 to allow sufficient time for mandatory facility
security clearance procedures to be completed. This information will be
transmitted to the CDC Security Office for approval. An email
confirming registration will be sent from NIOSH for both in-person
participation and audio conferencing participation.
Oral comments will be permitted for 15 minutes. If additional time
becomes available, presenters will be notified. All requests to present
should contain the name, address, telephone number, and relevant
business affiliations of the presenter, topic of the presentation,
whether you will be presenting in person or by phone, and the
approximate time requested for the presentation. An email confirming
registration will be sent from the NIOSH Docket Office and will include
details needed to participate. Oral comments given at the meeting will
be recorded and included in the docket.
After reviewing the requests for presentations, NIOSH will notify
the presenter when his/her presentation is scheduled. If a participant
is not in attendance when his/her presentation is scheduled to begin,
the remaining participants will be heard in order. After the last
scheduled speaker is heard, participants who missed their assigned
times may be allowed to speak, limited by time available.
Attendees who wish to speak but did not submit a request for the
opportunity to make a presentation may be given this opportunity after
the scheduled speakers are heard, at the discretion of the presiding
officer and limited by time available.
You may submit comments, identified by CDC 2016-0003 and NIOSH 057-
A, by either of the following methods:
Federal eRulemaking Portal: 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.
Instructions: All information received in response to this notice
must include the agency name and docket number [CDC-2016-0003; NIOSH
057-A]. All relevant comments received will be posted without change to
www.regulations.gov including any personal information provided. All
information will be available for public examination and copying at the
NIOSH Docket Office, 1150 Tusculum Avenue, Room 155, Cincinnati, Ohio
45226.
Non-U.S. Citizens: Because of CDC Security Regulations, any non-
U.S. citizen wishing to attend this meeting must provide the following
information in writing to the NIOSH Docket Officer at the address below
no later than February 24, 2016.
Name:
Gender:
Date of Birth:
Place of Birth (city, province, state, country):
Citizenship:
Passport Number:
Date of Passport Issue:
Date of Passport Expiration:
Type of Visa:
U.S. Naturalization Number (if a naturalized citizen):
U.S. Naturalization Date (if a naturalized citizen):
Visitor's Organization:
Organization Address:
Organization Telephone Number:
Visitor's Position/Title within the Organization:
This information will be transmitted to the CDC Security Office for
approval. Visitors will be notified as soon as approval has been
obtained.
Public Review
The external review of the draft document has been (1) developed in
accordance with Office of Management and Budget (OMB) guidelines, (2)
is consistent with NIOSH peer review practice, and (3) is meant to
ensure that credible and appropriate science is reflected within the
draft document.
Dated: February 4, 2016.
John Howard,
Director, National Institute for Occupational Safety and Health,
Centers for Disease Control and Prevention.
[FR Doc. 2016-02650 Filed 2-9-16; 8:45 am]
BILLING CODE 4163-19-P