Proposed Information Collection Activity; Refugee Support Services (RSS) and RSS Set Aside Sub-Agency List (0970-0556), 29788-29789 [2021-11653]
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Federal Register / Vol. 86, No. 105 / Thursday, June 3, 2021 / Notices
studies of silver nanomaterials in
animals and cellular systems. Based on
review of the scientific literature,
NIOSH revised the draft CIB and
developed a recommended exposure
limit (REL) for silver nanomaterials. The
revised draft CIB was released for public
review with a Federal Register notice
on September 18, 2018 [83 FR 47174].
The notice included a request for
comments from peer reviewers and the
public and provided information
regarding a second public meeting that
was held on October 30, 2018. The
purpose of the public review was to
obtain comments on whether the NIOSH
draft document (1) adequately and
clearly described the scientific literature
on the potential adverse health effects of
silver nanomaterials, and (2)
demonstrated that the NIOSH
recommendations on occupational
exposure to silver nanomaterials are
consistent with current scientific
knowledge. Public, stakeholder, and
scientific peer reviewers were given the
opportunity to submit comments to the
docket by November 30, 2018.
NIOSH carefully considered the
comments received on the revised draft
document. Reviewers provided
comments on the NIOSH assessment of
the potential adverse health effects of
occupational exposure to silver
nanomaterials, on the data and methods
NIOSH used to develop a recommended
exposure limit for silver nanomaterials,
on the NIOSH recommended methods
for assessing and controlling exposures
to silver nanomaterials in the
workplace, and on the identified data
gaps and future research needs. In
developing the final document, NIOSH
performed an additional systematic
literature search in April 2019 to
determine if any subsequent studies in
animals or humans had been published
that pertained to the quantitative risk
assessment and the derivation of a REL
for silver nanomaterials. No additional
studies were found that impacted those
topics. NIOSH responded to the public,
stakeholder, and peer review comments
received and developed the final
document consistent with the responses
to comments. These comments and the
NIOSH responses are available at:
https://www.regulations.gov/search/
docket?filter=cdc-2016-0001.
The final CIB provides a
comprehensive scientific review of the
scientific literature pertaining to
occupational exposure to silver
nanomaterials. The literature includes
studies of exposures to silver
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nanomaterials in the workplace,
toxicological effects of exposure to
silver nanomaterials in experimental
animal and cellular systems, and effects
of particle size and other properties on
the toxicological effects of silver. NIOSH
assessed the potential health risks of
occupational exposure to silver
nanomaterials by evaluating the
scientific literature. Studies in animals
have shown adverse lung and liver
effects associated with exposure to
silver nanoparticles. Based on an
assessment of those data, NIOSH
developed a REL for silver
nanomaterials. This new REL applies to
processes that produce or use silver
nanomaterials in the workplace. In
addition, NIOSH continues to
recommend its existing REL for total
silver (metal dust and soluble
compounds, as Ag) [www.cdc.gov/
niosh/npg/npgd0557.html]. In the CIB,
NIOSH provides recommendations on
the measurement and control of
occupational exposures to silver and
silver nanomaterials.
NIOSH further recommends the use of
workplace exposure assessments,
engineering controls, safe work
procedures, training, and education, and
established medical surveillance
approaches to prevent potential adverse
health effects from occupational
exposure to silver nanomaterials.
NIOSH proposes research needed to fill
remaining data gaps on the potential
adverse health effects of occupational
exposure to silver nanomaterials.
John J. Howard,
Director, National Institute for Occupational
Safety and Health, Centers for Disease Control
and Prevention.
[FR Doc. 2021–11626 Filed 6–2–21; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Refugee Support Services
(RSS) and RSS Set Aside Sub-Agency
List (0970–0556)
Office of Refugee Resettlement,
Administration for Children and
Families, HHS.
ACTION: Request for public comment.
AGENCY:
The Administration for
Children and Families (ACF) Office of
SUMMARY:
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Refugee Resettlement (ORR) seeks
approval for a revision to an existing
information collection, requesting
Refugee Support Services (RSS) grantees
and RSS Set Aside grantees to provide
the agency name, city, state, website,
and funding amount for each contracted
sub-grantee. Additionally, ORR seeks
approval to have the option to make this
information public. This would enhance
the accessibility of refugee service
provider information to eligible clients
in support of the service referral
responsibilities of the State Refugee
Coordinators. Similar information for
ORR’s discretionary grants is currently
made public.
Comments due within 60 days of
publication. In compliance with the
requirements of the Paperwork
Reduction Act of 1995, ACF is soliciting
public comment on the specific aspects
of the information collection described
above.
DATES:
Copies of the proposed
collection of information can be
obtained and comments may be
forwarded by emailing infocollection@
acf.hhs.gov. Alternatively, copies can
also be obtained by writing to the
Administration for Children and
Families, Office of Planning, Research,
and Evaluation (OPRE), 330 C Street
SW, Washington, DC 20201, Attn: ACF
Reports Clearance Officer. All requests,
emailed or written, should be identified
by the title of the information collection.
ADDRESSES:
SUPPLEMENTARY INFORMATION:
Description: This data collection
requests RSS grantees and RSS Set
Aside grantees to provide the agency
name, city, state, website, and funding
amount for each contracted sub-grantee.
The information will be used for
national resource mapping pertaining to
ORR RSS funding at the local level.
Improved communication and the
knowledge of all local providers is
important to ORR’s overall oversight of
the program. In addition to RSS formula
funding to states and state replacement
agencies who then issue sub-awards to
local providers, ORR also awards
discretionary grants that directly fund
local refugee service providers. This
report will provide ORR a complete
picture of the availability all ORR
resources to assist newly arrived
refugees at the local level increasing our
ability to identify gaps or target areas of
need.
Respondents: State governments and
replacement designees.
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Federal Register / Vol. 86, No. 105 / Thursday, June 3, 2021 / Notices
ANNUAL BURDEN ESTIMATES
Instrument
Total number
of respondents
Total number
of responses
per
respondent
Average
burden hours
per response
Total burden
hours
Annual burden
hours
RSS and RSS Set Aside Sub-grantee List .........................
56
3
2
336
112
Estimated Total Annual Burden
Hours: 112.
Comments: The Department
specifically requests comments on (a)
whether the proposed collection of
information is necessary for the proper
performance of the functions of the
agency, including whether the
information shall have practical utility;
(b) the accuracy of the agency’s estimate
of the burden of the proposed collection
of information; (c) the quality, utility,
and clarity of the information to be
collected; and (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology. Consideration will be given
to comments and suggestions submitted
within 60 days of this publication.
Authority: Refugee Act of 1980
[Immigration and Nationality Act, Title IV,
Chapter 2 Section 412 (e)] and 45 CFR
400.28.
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2021–11653 Filed 6–2–21; 8:45 am]
BILLING CODE 4184–45–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2021–D–0391]
Oral Drug Products Administered via
Enteral Feeding Tube: In Vitro Testing
and Labeling Recommendations; Draft
Guidance for Industry; Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice of availability.
The Food and Drug
Administration (FDA or Agency) is
announcing the availability of a draft
guidance for industry entitled ‘‘Oral
Drug Products Administered Via Enteral
Feeding Tube: In Vitro Testing and
Labeling Recommendations.’’ This draft
guidance provides recommendations for
consistent in vitro testing of oral drug
products to demonstrate their suitability
to be administered via enteral tube. In
addition, it supports the development of
clear product-specific enteral tube
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administration instructions in labeling
for administration to patients unable to
ingest oral drug products.
DATES: Submit either electronic or
written comments on the draft guidance
by August 2, 2021 to ensure that the
Agency considers your comment on this
draft guidance before it begins work on
the final version of the guidance.
ADDRESSES: You may submit comments
on any guidance at any time as follows:
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
information submitted, marked and
identified, as confidential, if submitted
as detailed in ‘‘Instructions.’’
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Instructions: All submissions received
must include the Docket No. FDA–
2021–D–0391 for ‘‘Oral Drug Products
Administered Via Enteral Feeding Tube:
In Vitro Testing and Labeling
Recommendations.’’ Received
comments 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, 240–402–7500.
• 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.govinfo.gov/content/pkg/FR-201509-18/pdf/2015-23389.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
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]]>Agencies
[Federal Register Volume 86, Number 105 (Thursday, June 3, 2021)]
[Notices]
[Pages 29788-29789]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-11653]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Refugee Support
Services (RSS) and RSS Set Aside Sub-Agency List (0970-0556)
AGENCY: Office of Refugee Resettlement, Administration for Children and
Families, HHS.
ACTION: Request for public comment.
-----------------------------------------------------------------------
SUMMARY: The Administration for Children and Families (ACF) Office of
Refugee Resettlement (ORR) seeks approval for a revision to an existing
information collection, requesting Refugee Support Services (RSS)
grantees and RSS Set Aside grantees to provide the agency name, city,
state, website, and funding amount for each contracted sub-grantee.
Additionally, ORR seeks approval to have the option to make this
information public. This would enhance the accessibility of refugee
service provider information to eligible clients in support of the
service referral responsibilities of the State Refugee Coordinators.
Similar information for ORR's discretionary grants is currently made
public.
DATES: Comments due within 60 days of publication. In compliance with
the requirements of the Paperwork Reduction Act of 1995, ACF is
soliciting public comment on the specific aspects of the information
collection described above.
ADDRESSES: Copies of the proposed collection of information can be
obtained and comments may be forwarded by emailing
[email protected]. Alternatively, copies can also be obtained
by writing to the Administration for Children and Families, Office of
Planning, Research, and Evaluation (OPRE), 330 C Street SW, Washington,
DC 20201, Attn: ACF Reports Clearance Officer. All requests, emailed or
written, should be identified by the title of the information
collection.
SUPPLEMENTARY INFORMATION:
Description: This data collection requests RSS grantees and RSS Set
Aside grantees to provide the agency name, city, state, website, and
funding amount for each contracted sub-grantee.
The information will be used for national resource mapping
pertaining to ORR RSS funding at the local level. Improved
communication and the knowledge of all local providers is important to
ORR's overall oversight of the program. In addition to RSS formula
funding to states and state replacement agencies who then issue sub-
awards to local providers, ORR also awards discretionary grants that
directly fund local refugee service providers. This report will provide
ORR a complete picture of the availability all ORR resources to assist
newly arrived refugees at the local level increasing our ability to
identify gaps or target areas of need.
Respondents: State governments and replacement designees.
[[Page 29789]]
Annual Burden Estimates
--------------------------------------------------------------------------------------------------------------------------------------------------------
Total number of Average burden
Instrument Total number of responses per hours per Total burden Annual burden
respondents respondent response hours hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
RSS and RSS Set Aside Sub-grantee List............................. 56 3 2 336 112
--------------------------------------------------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 112.
Comments: The Department specifically requests comments on (a)
whether the proposed collection of information is necessary for the
proper performance of the functions of the agency, including whether
the information shall have practical utility; (b) the accuracy of the
agency's estimate of the burden of the proposed collection of
information; (c) the quality, utility, and clarity of the information
to be collected; and (d) ways to minimize the burden of the collection
of information on respondents, including through the use of automated
collection techniques or other forms of information technology.
Consideration will be given to comments and suggestions submitted
within 60 days of this publication.
Authority: Refugee Act of 1980 [Immigration and Nationality
Act, Title IV, Chapter 2 Section 412 (e)] and 45 CFR 400.28.
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2021-11653 Filed 6-2-21; 8:45 am]
BILLING CODE 4184-45-P
