Survey of Nanomaterial Risk Management Practices, 36784-36785 [2013-14564]
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36784
Federal Register / Vol. 78, No. 118 / Wednesday, June 19, 2013 / Notices
of informed consent issues in cluster
randomized trials. After lunch, there
will be a special expert panel discussing
Certificates of Confidentiality (COCs).
Following opening remarks on the
morning of July 11, the Subpart A
Subcommittee (SAS) will give their
report. This will be followed by a
discussion of the concept of engagement
in human subjects research. SAS is
charged with developing
recommendations for consideration by
SACHRP regarding the application of
subpart A of 45 CFR part 46 in the
current research environment; this
Subcommittee was established by
SACHRP in October 2006. The day will
conclude with a panel discussion of
issues surrounding electronic informed
consent.
Public attendance at the meeting is
limited to space available. Individuals
who plan to attend the meeting and
need special assistance, such as sign
language interpretation or other
reasonable accommodations, should
notify the designated contact persons.
Members of the public will have the
opportunity to provide comments on
both days of the meeting. Public
comment will be limited to five minutes
per speaker. Any members of the public
who wish to have printed materials
distributed to SACHRP members for this
scheduled meeting should submit
materials to the Executive Director,
SACHRP, prior to the close of business
July 5, 2013.
Dated: June 12, 2013.
Jerry Menikoff,
Director, Office for Human Research
Protections, Executive Secretary, Secretary’s
Advisory Committee on Human Research
Protections.
[FR Doc. 2013–14518 Filed 6–18–13; 8:45 am]
BILLING CODE 4150–36–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention (CDC)
[CDC–2013–0010, Docket Number NIOSH–
265]
mstockstill on DSK4VPTVN1PROD with NOTICES
Survey of Nanomaterial Risk
Management Practices
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: Proposed NIOSH Survey of
Nanomaterial Risk Management
AGENCY:
VerDate Mar<15>2010
17:13 Jun 18, 2013
Jkt 229001
Practices; Notice of Public Meeting and
Request for Comments.
SUMMARY: The National Institute for
Occupational Safety and Health
(NIOSH) of the Centers for Disease
Control and Prevention (CDC)
announces a public meeting and
opportunity for comment on a proposed
NIOSH survey. The primary purpose of
the survey is to evaluate the use of
NIOSH guidelines and risk mitigation
practices for safe handling of engineered
nanomaterials (ENMs) in the workplace.
Information collected from the survey
will be useful in future revisions of the
guidelines. The public is invited to
comment on the proposed survey
through a public docket and/or
participation in a one-day public
meeting.
To view the notice and related
materials, visit https://
www.regulations.gov and enter CDC–
2013–0010 in the search field and click
‘‘Search.’’
Public comment period: Submit either
electronic or written comments by
September 15, 2013.
Registration to attend the meeting
must be received by July 17, 2013 and
will be accepted on a first come first
served basis. See the SUPPLEMENTARY
INFORMATION section for information on
how to register for the meeting.
ADDRESSES: The public meeting will be
held at the NIOSH Alice Hamilton
building, 5555 Ridge Avenue,
Cincinnati, OH 45213. The public
meeting will be held on July 31, 2013,
from 8 a.m. to 3:00 p.m. EDT.
Security Considerations: Due to
mandatory security clearance
procedures at the NIOSH Alice
Hamilton building, in-person attendees
must present valid government-issued
picture identification to security
personnel upon entering the parking lot.
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 June
29, 2013 to allow time for mandatory
CDC facility security clearance
procedures to be completed.
1. Name:
2. Gender:
3. Date of Birth:
4. Place of birth (city, province, state,
country):
5. Citizenship:
6. Passport Number:
7. Date of Passport Issue:
8. Date of Passport Expiration:
9. Type of Visa:
10. U.S. Naturalization Number (if a
naturalized citizen):
PO 00000
Frm 00042
Fmt 4703
Sfmt 4703
11. U.S. Naturalization Date (if a
naturalized citizen):
12. Visitor’s Organization:
13. Organization Address:
14. Organization Telephone Number:
15. 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.
You may submit comments, identified
by CDC–2013–0010 and Docket Number
NIOSH–265, by either of the following
two methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: NIOSH Docket Office, Robert
A. Taft Laboratories, 4676 Columbia
Parkway, MS C–34, Cincinnati, Ohio
45226.
Instructions: All information received
in response to this notice must include
the agency name and docket number
(CDC–2013–0010; NIOSH–265). All
relevant comments received will be
posted without change to https://
www.regulations.gov, including any
personal information provided. All
electronic comments should be
formatted as Microsoft Word. Please
make reference to CDC–2013–0010 and
Docket Number NIOSH–265.
SUPPLEMENTARY INFORMATION:
Attendance: The meeting is open to the
public, limited only by the capacity (80)
of the conference room. Confirm your
attendance to this meeting by sending
an email to jun1@cdc.gov by July 17,
2013. An email confirming registration
will be sent from NIOSH and will
include details needed to participate.
Oral comments given at the meeting will
be recorded and included in the NIOSH
Docket Number 265.
Background: NIOSH is among the
world’s leaders in promoting the safe
and responsible development and use of
ENMs. NIOSH has published guidelines
on the safe use of ENMs including
‘‘Approaches to Safe Nanotechnology:
Managing the Health and Safety
Concerns Associated with Engineered
Nanomaterials’’ (https://www.cdc.gov/
niosh/docs/2009–125/pdfs/2009–
125.pdf) and ‘‘General Safe Practices for
Working With Engineered
Nanomaterials in Research
Laboratories’’ (https://www.cdc.gov/
niosh/docs/2012–147/pdfs/2012–
147.pdf). Other organizations in the U.S.
and around the world have also
developed guidelines for the safe use of
ENMs. The proposed survey will
examine the extent to which these and
other guidelines are implemented and
the barriers to using the guidelines.
E:\FR\FM\19JNN1.SGM
19JNN1
36785
Federal Register / Vol. 78, No. 118 / Wednesday, June 19, 2013 / Notices
A draft questionnaire is available for
review at https://www.regulations.gov.
NIOSH requests public input on the
content of the questionnaire and
consideration of the following:
(1) Apart from a survey, what
alternative methods should be
considered to gather this information?
(2) What resources are available that
can be used to identify nanomaterial
producers, distributors, end-users, and
R&D laboratories for inclusion in a
sampling frame?
(3) A web-based survey is being
proposed primarily because it is costefficient and can be easy to administer.
Should any other modes (telephone,
mail) be considered?
(4) In small and medium-sized
establishments, who would be the
person best suited to respond to
questions addressing risk management
practices for ENMs?
(5) What should be the maximum
amount of time needed to complete the
survey?
(6) Is benchmarking adherence to safe
use guidelines of value to your
organization?
(7) What guidelines are being used by
your organization to minimize worker
exposure to ENMs?
(8) Are there any questions in the
draft survey that should be excluded?
Are there any questions not included in
the draft survey that should be
included?
FOR FURTHER INFORMATION CONTACT: Jim
Boiano—jboiano@cdc.gov; 513–841–
4246 or Rebecca Tsai—rtsai@cdc.gov;
513–841–4398, NIOSH, 4676 Columbia
Parkway, Mail Stop R17, Cincinnati,
Ohio 45226–1998.
Dated: June 13, 2013.
John Howard,
Director, National Institute for Occupational
Safety and Health, Centers for Disease Control
and Prevention.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Administration for Children and
Families
Disease, Disability, and Injury
Prevention and Control Special
Emphasis Panel (SEP): Initial Review
Submission for OMB Review;
Comment Request
The meeting announced below
concerns Centers for Disease Control
and Prevention Public Health
Preparedness and Response Research to
Aid Recovery from Hurricane Sandy,
Request for Application (RFA) TP13–
001, initial review.
Correction: The notice was published
in the Federal Register on June 11,
2013, Volume 78, Number 112, Pages
35035—35036. The time, date and place
should read as follows:
Time and Date: 12:00 p.m.–5:00 p.m.
(EST), July 10, 2013 (Closed).
Place: Teleconference.
Contact Person for More Information:
Shoukat Qari, D.V.M., Ph.D., Scientific
Review Officer, CDC, 1600 Clifton Road,
NE., Mailstop K72, Atlanta, Georgia
30333, Telephone: (770) 488–8808.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
management activities, for both the
Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Dana Redford,
Acting Director, Management Analysis and
Services Office, Centers for Disease Control
and Prevention.
[FR Doc. 2013–14541 Filed 6–18–13; 8:45 am]
BILLING CODE 4163–18–P
Title: National Medical Support
Notice
OMB No.: 0970–0222
Description: The National Medical
Support Notice (NMSN) is a two-part
document that requires information
from State child support enforcement
agencies, employers, and health plan
administrators to assist in enforcing
health care coverage provisions in a
child support order. The Department of
Health and Human Services (DHHS),
Administration for Children and
Families (ACF) developed and
maintains Part A of the NMSN, which
is sent to an obligor’s employer for
completion; the Department of Labor
(DOL) developed and maintains Part B
of the NMSN, which is provided to
health care administrators following
completion of Part A.
DOL revised Part B to conform with
changes to the currently approved Part
A and is seeking a three year approval
from OMB. To avoid burdening the
State child support enforcement
agencies with potential reprogramming
at varying times due to future changes
in either Part A or Part B, ACF is
resubmitting an unchanged information
collection package and requesting an
extension to the current OMB approval
of NMSN Part A to synchronize the
expiration date with NMSN Part B.
Respondents: State child support
enforcement agencies, employers, and
health plan administrators.
[FR Doc. 2013–14564 Filed 6–18–13; 8:45 am]
BILLING CODE 4163–19–P
ANNUAL BURDEN ESTIMATES
Number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total burden
hours
National Medical Support Notice—Part A—Notice To Withhold for Health
Care Coverage .............................................................................................
mstockstill on DSK4VPTVN1PROD with NOTICES
Instrument
54
97,775
0.17
897,574.50
Estimated Total Annual Burden
Hours: 897,574.50.
Additional Information:
Copies of the proposed collection may
be obtained by writing to the
Administration for Children and
Families, Office of Planning, Research
VerDate Mar<15>2010
17:13 Jun 18, 2013
Jkt 229001
and Evaluation, 370 L’Enfant
Promenade, SW., Washington, DC
20447, Attn: ACF Reports Clearance
Officer. All requests should be
identified by the title of the information
collection. Email address:
infocollection@acf.hhs.gov.
PO 00000
Frm 00043
Fmt 4703
Sfmt 4703
OMB Comment:
OMB is required to make a decision
concerning the collection of information
between 30 and 60 days after
publication of this document in the
Federal Register. Therefore, a comment
is best assured of having its full effect
E:\FR\FM\19JNN1.SGM
19JNN1
Agencies
[Federal Register Volume 78, Number 118 (Wednesday, June 19, 2013)]
[Notices]
[Pages 36784-36785]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-14564]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention (CDC)
[CDC-2013-0010, Docket Number NIOSH-265]
Survey of Nanomaterial Risk Management Practices
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: Proposed NIOSH Survey of Nanomaterial Risk Management
Practices; Notice of Public Meeting and Request for Comments.
-----------------------------------------------------------------------
SUMMARY: The National Institute for Occupational Safety and Health
(NIOSH) of the Centers for Disease Control and Prevention (CDC)
announces a public meeting and opportunity for comment on a proposed
NIOSH survey. The primary purpose of the survey is to evaluate the use
of NIOSH guidelines and risk mitigation practices for safe handling of
engineered nanomaterials (ENMs) in the workplace. Information collected
from the survey will be useful in future revisions of the guidelines.
The public is invited to comment on the proposed survey through a
public docket and/or participation in a one-day public meeting.
To view the notice and related materials, visit https://www.regulations.gov and enter CDC-2013-0010 in the search field and
click ``Search.''
Public comment period: Submit either electronic or written comments
by September 15, 2013.
Registration to attend the meeting must be received by July 17,
2013 and will be accepted on a first come first served basis. See the
SUPPLEMENTARY INFORMATION section for information on how to register
for the meeting.
ADDRESSES: The public meeting will be held at the NIOSH Alice Hamilton
building, 5555 Ridge Avenue, Cincinnati, OH 45213. The public meeting
will be held on July 31, 2013, from 8 a.m. to 3:00 p.m. EDT.
Security Considerations: Due to mandatory security clearance
procedures at the NIOSH Alice Hamilton building, in-person attendees
must present valid government-issued picture identification to security
personnel upon entering the parking lot.
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 June 29, 2013 to allow time for mandatory CDC facility
security clearance procedures to be completed.
1. Name:
2. Gender:
3. Date of Birth:
4. Place of birth (city, province, state, country):
5. Citizenship:
6. Passport Number:
7. Date of Passport Issue:
8. Date of Passport Expiration:
9. Type of Visa:
10. U.S. Naturalization Number (if a naturalized citizen):
11. U.S. Naturalization Date (if a naturalized citizen):
12. Visitor's Organization:
13. Organization Address:
14. Organization Telephone Number:
15. 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.
You may submit comments, identified by CDC-2013-0010 and Docket
Number NIOSH-265, by either of the following two methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the instructions for submitting comments.
Mail: NIOSH Docket Office, Robert A. Taft Laboratories,
4676 Columbia Parkway, MS C-34, Cincinnati, Ohio 45226.
Instructions: All information received in response to this notice
must include the agency name and docket number (CDC-2013-0010; NIOSH-
265). All relevant comments received will be posted without change to
https://www.regulations.gov, including any personal information
provided. All electronic comments should be formatted as Microsoft
Word. Please make reference to CDC-2013-0010 and Docket Number NIOSH-
265.
SUPPLEMENTARY INFORMATION: Attendance: The meeting is open to the
public, limited only by the capacity (80) of the conference room.
Confirm your attendance to this meeting by sending an email to
jun1@cdc.gov by July 17, 2013. An email confirming registration will be
sent from NIOSH and will include details needed to participate. Oral
comments given at the meeting will be recorded and included in the
NIOSH Docket Number 265.
Background: NIOSH is among the world's leaders in promoting the
safe and responsible development and use of ENMs. NIOSH has published
guidelines on the safe use of ENMs including ``Approaches to Safe
Nanotechnology: Managing the Health and Safety Concerns Associated with
Engineered Nanomaterials'' (https://www.cdc.gov/niosh/docs/2009-125/pdfs/2009-125.pdf) and ``General Safe Practices for Working With
Engineered Nanomaterials in Research Laboratories'' (https://www.cdc.gov/niosh/docs/2012-147/pdfs/2012-147.pdf). Other organizations
in the U.S. and around the world have also developed guidelines for the
safe use of ENMs. The proposed survey will examine the extent to which
these and other guidelines are implemented and the barriers to using
the guidelines.
[[Page 36785]]
A draft questionnaire is available for review at https://www.regulations.gov.
NIOSH requests public input on the content of the questionnaire and
consideration of the following:
(1) Apart from a survey, what alternative methods should be
considered to gather this information?
(2) What resources are available that can be used to identify
nanomaterial producers, distributors, end-users, and R&D laboratories
for inclusion in a sampling frame?
(3) A web-based survey is being proposed primarily because it is
cost-efficient and can be easy to administer. Should any other modes
(telephone, mail) be considered?
(4) In small and medium-sized establishments, who would be the
person best suited to respond to questions addressing risk management
practices for ENMs?
(5) What should be the maximum amount of time needed to complete
the survey?
(6) Is benchmarking adherence to safe use guidelines of value to
your organization?
(7) What guidelines are being used by your organization to minimize
worker exposure to ENMs?
(8) Are there any questions in the draft survey that should be
excluded? Are there any questions not included in the draft survey that
should be included?
FOR FURTHER INFORMATION CONTACT: Jim Boiano_jboiano@cdc.gov; 513-841-
4246 or Rebecca Tsai_rtsai@cdc.gov; 513-841-4398, NIOSH, 4676 Columbia
Parkway, Mail Stop R17, Cincinnati, Ohio 45226-1998.
Dated: June 13, 2013.
John Howard,
Director, National Institute for Occupational Safety and Health,
Centers for Disease Control and Prevention.
[FR Doc. 2013-14564 Filed 6-18-13; 8:45 am]
BILLING CODE 4163-19-P