Proposed Information Collection Activity; Refugee Support Services (RSS) and RSS Set Aside Sub-Agency List (0970-0556), 29788-29789 [2021-11653]

Download as PDF khammond on DSKJM1Z7X2PROD with NOTICES 29788 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 VerDate Sep<11>2014 17:23 Jun 02, 2021 Jkt 253001 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: PO 00000 Frm 00052 Fmt 4703 Sfmt 4703 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. E:\FR\FM\03JNN1.SGM 03JNN1 29789 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 khammond on DSKJM1Z7X2PROD with NOTICES SUMMARY: VerDate Sep<11>2014 17:23 Jun 02, 2021 Jkt 253001 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.’’ PO 00000 Frm 00053 Fmt 4703 Sfmt 4703 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 E:\FR\FM\03JNN1.SGM 03JNN1

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]


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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