Submission for OMB Review; Generic Clearance for the Comprehensive Child Welfare Information System (CCWIS) Review and Technical Assistance Process (New Collection), 86936-86937 [2020-28925]

Download as PDF 86936 Federal Register / Vol. 85, No. 251 / Thursday, December 31, 2020 / Notices Services as the Privacy Act permits, including in accordance with the routine uses published for this system in the Federal Register, and as authorized by law. Such lawful purposes may include but are not limited to sharing identifiable information with state and local public health departments, and other cooperating authorities. CDC and cooperating authorities will retain, use, delete, or otherwise destroy the designated information in accordance with federal law and the System of Records Notice (SORN) set forth above. You may contact the system manager at dgmqpolicyoffice@cdc.gov; Division of Global Migration and Quarantine, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS H16–4, Atlanta, GA 30329, if you have questions about CDC’s use of your data. Authority The authority for these orders is Sections 361 and 365 of the Public Health Service Act (42 U.S.C. 264) and 42 CFR 71.20 & 71.31(b). Nina B. Witkofsky, Acting Chief of Staff, Centers for Disease Control and Prevention. [FR Doc. 2020–28981 Filed 12–28–20; 4:15 pm] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for OMB Review; Generic Clearance for the Comprehensive Child Welfare Information System (CCWIS) Review and Technical Assistance Process (New Collection) Children’s Bureau, Administration for Children and Families, HHS. ACTION: Request for public comment. AGENCY: The Children’s Bureau (CB), Administration for Children and Families (ACF), U.S. Department of Health and Human Services (HHS), is proposing to establish a generic clearance to collect information to assess regulatory requirements of title IV–E agencies’ Comprehensive Child Welfare Information System (CCWIS) and ensure that the CCWIS is utilized for purposes consistent with the efficient, economical, and effective administration of the title IV–B and IV– E plans. The information collected is intended to be used for review and technical assistance processes. DATES: Comments due within 30 days of publication. OMB must make a decision about 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 if OMB receives it within 30 days of publication. ADDRESSES: Written comments and recommendations for the proposed information collection should be sent within 30 days of publication of this SUMMARY: notice to www.reginfo.gov/public/do/ PRAMain. Find this particular information collection by selecting ‘‘Currently under 30-day Review—Open for Public Comments’’ or by using the search function. SUPPLEMENTARY INFORMATION: Description: This initial request is to establish an overarching generic for CCWIS Review and Technical Assistance (TA) information collections and includes six initial TA tools for title IV–E agencies to self-assess their conformity to CCWIS project and design requirements at 45 CFR 1355.52–3. The initial six TA tools include intake, investigation, case management, adoption, foster care and service provider management, and administration. In the future, ACF will submit under this generic clearance mechanism additional TA tools for title IV–E agencies to self-assess design, data quality, usability, reporting, data exchanges, external systems, eligibility, finance, Child Welfare Contributing Agencies, and other tools, as needed, to assess new child welfare programs and modern system architecture. The CCWIS requirements at 45 CFR 1355.55 require the review, assessment, and inspection of the planning, design, development, installation, operation, and maintenance of each CCWIS project on a continuing basis. The Advance Planning Document regulations at 45 CFR 95.621 require periodic reviews of state and local agency methods and practices to insure that information systems, including CCWIS, are utilized for purposes consistent with proper and efficient administration. Respondents: Title IV–E agencies under the Social Security Act. ANNUAL BURDEN ESTIMATES Total number of respondents Instrument khammond on DSKJM1Z7X2PROD with NOTICES CCWIS Self-Assessment—Intake .................................................................... CCWIS Self-Assessment—Investigation ......................................................... CCWIS Self-Assessment—Case Management ............................................... CCWIS Self-Assessment—Adoption ............................................................... CCWIS Self-Assessment—Foster Care and Service Provider Management CCWIS Self-Assessment—Administration ....................................................... Future Tools to be Developed ......................................................................... VerDate Sep<11>2014 19:28 Dec 30, 2020 Jkt 253001 PO 00000 Frm 00036 Fmt 4703 Sfmt 9990 Total number of responses per respondent 55 55 55 55 55 55 55 E:\FR\FM\31DEN1.SGM 1 1 1 1 1 1 10 31DEN1 Average burden hours per response Total burden hours 10 10 10 10 10 10 12 550 550 550 550 550 550 6,600 Federal Register / Vol. 85, No. 251 / Thursday, December 31, 2020 / Notices Estimated Total Annual Burden Hours: 9,900. Agency guidances at any time as follows: Authority: 5 U.S.C. 301; 42 U.S.C. 470, 620 et seq., 622(b), 629b(a), 652(b), 654A, 670 et seq., 671(a), 1302, and 1396a(a). 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’’). Mary B. Jones, ACF/OPRE Certifying Officer. [FR Doc. 2020–28925 Filed 12–30–20; 8:45 am] BILLING CODE 4184–25–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2016–N–0124 (Formerly Docket No. FDA–1975–N–0012)] Consumer Antiseptic Rub Final Rule; Finding of Ineligibility for Inclusion in Final Monograph Questions and Answers; Guidance for Industry; Small Entity Compliance Guide; 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 final guidance for industry entitled ‘‘Consumer Antiseptic Rub Final Rule Questions and Answers.’’ We are issuing this guidance in accordance with the Small Business Regulatory Enforcement Fairness Act to help small businesses understand and comply with the Consumer Antiseptic Rub Final Rule; Finding of Ineligibility for Inclusion in Final Monograph (Consumer Antiseptic Rub FR). In the Consumer Antiseptic Rub FR, FDA established that 28 active ingredients used in nonprescription (also known as over-the-counter (OTC)) consumer antiseptic products intended for use without water (consumer antiseptic rubs) are not eligible for evaluation under FDA’s OTC Drug Review, which was used to evaluate the safety and effectiveness of OTC drug products marketed in the United States on or before May 1972. The Consumer Antiseptic Rub FR also established that three active ingredients used in consumer antiseptic rubs are eligible for evaluation under the OTC Drug Review and granted requests to temporarily defer further rulemaking on these three eligible ingredients to allow for the development and submission of new safety and effectiveness data. DATES: The announcement of the guidance is published in the Federal Register on December 31, 2020. ADDRESSES: You may submit either electronic or written comments on khammond on DSKJM1Z7X2PROD with NOTICES SUMMARY: VerDate Sep<11>2014 19:28 Dec 30, 2020 Jkt 253001 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.’’ Instructions: All submissions received must include the Docket No. FDA– 2016–N–0124 for ‘‘Consumer Antiseptic Rub Final Rule Questions and Answers.’’ 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 PO 00000 Frm 00037 Fmt 4703 Sfmt 4703 86937 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 Staff, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852, 240–402–7500. You may submit comments on any guidance at any time (see 21 CFR 10.115(g)(5)). Submit written requests for single copies of this guidance to the Division of Drug Information, Center for Drug Evaluation and Research, Food and Drug Administration, 10001 New Hampshire Ave., Hillandale Building, 4th Floor, Silver Spring, MD 20993– 0002. Send one self-addressed adhesive label to assist that office in processing your requests. See the SUPPLEMENTARY INFORMATION section for electronic access to the guidance document. FOR FURTHER INFORMATION CONTACT: Anita Kumar, Center for Drug Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 22, Rm. 5445, Silver Spring, MD 20993–0002, 301– 796–1032. SUPPLEMENTARY INFORMATION: I. Background FDA is announcing the availability of a guidance for industry entitled ‘‘Consumer Antiseptic Rub Final Rule E:\FR\FM\31DEN1.SGM 31DEN1

Agencies

[Federal Register Volume 85, Number 251 (Thursday, December 31, 2020)]
[Notices]
[Pages 86936-86937]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-28925]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Submission for OMB Review; Generic Clearance for the 
Comprehensive Child Welfare Information System (CCWIS) Review and 
Technical Assistance Process (New Collection)

AGENCY: Children's Bureau, Administration for Children and Families, 
HHS.

ACTION: Request for public comment.

-----------------------------------------------------------------------

SUMMARY: The Children's Bureau (CB), Administration for Children and 
Families (ACF), U.S. Department of Health and Human Services (HHS), is 
proposing to establish a generic clearance to collect information to 
assess regulatory requirements of title IV-E agencies' Comprehensive 
Child Welfare Information System (CCWIS) and ensure that the CCWIS is 
utilized for purposes consistent with the efficient, economical, and 
effective administration of the title IV-B and IV-E plans. The 
information collected is intended to be used for review and technical 
assistance processes.

DATES: Comments due within 30 days of publication. OMB must make a 
decision about 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 if OMB receives it 
within 30 days of publication.

ADDRESSES: Written comments and recommendations for the proposed 
information collection should be sent within 30 days of publication of 
this notice to www.reginfo.gov/public/do/PRAMain. Find this particular 
information collection by selecting ``Currently under 30-day Review--
Open for Public Comments'' or by using the search function.

SUPPLEMENTARY INFORMATION: 
    Description: This initial request is to establish an overarching 
generic for CCWIS Review and Technical Assistance (TA) information 
collections and includes six initial TA tools for title IV-E agencies 
to self-assess their conformity to CCWIS project and design 
requirements at 45 CFR 1355.52-3. The initial six TA tools include 
intake, investigation, case management, adoption, foster care and 
service provider management, and administration.
    In the future, ACF will submit under this generic clearance 
mechanism additional TA tools for title IV-E agencies to self-assess 
design, data quality, usability, reporting, data exchanges, external 
systems, eligibility, finance, Child Welfare Contributing Agencies, and 
other tools, as needed, to assess new child welfare programs and modern 
system architecture.
    The CCWIS requirements at 45 CFR 1355.55 require the review, 
assessment, and inspection of the planning, design, development, 
installation, operation, and maintenance of each CCWIS project on a 
continuing basis. The Advance Planning Document regulations at 45 CFR 
95.621 require periodic reviews of state and local agency methods and 
practices to insure that information systems, including CCWIS, are 
utilized for purposes consistent with proper and efficient 
administration.
    Respondents: Title IV-E agencies under the Social Security Act.

                                             Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
                                                                   Total  number
                                                   Total  number   of  responses      Average      Total burden
                   Instrument                           of              per        burden  hours       hours
                                                    respondents     respondent     per  response
----------------------------------------------------------------------------------------------------------------
CCWIS Self-Assessment--Intake...................              55               1              10             550
CCWIS Self-Assessment--Investigation............              55               1              10             550
CCWIS Self-Assessment--Case Management..........              55               1              10             550
CCWIS Self-Assessment--Adoption.................              55               1              10             550
CCWIS Self-Assessment--Foster Care and Service                55               1              10             550
 Provider Management............................
CCWIS Self-Assessment--Administration...........              55               1              10             550
Future Tools to be Developed....................              55              10              12           6,600
----------------------------------------------------------------------------------------------------------------


[[Page 86937]]

    Estimated Total Annual Burden Hours: 9,900.

    Authority: 5 U.S.C. 301; 42 U.S.C. 470, 620 et seq., 622(b), 
629b(a), 652(b), 654A, 670 et seq., 671(a), 1302, and 1396a(a).

Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2020-28925 Filed 12-30-20; 8:45 am]
BILLING CODE 4184-25-P