Agency Information Collection Activities: Proposed Collection: Public Comment Request; Information Collection Request Title: MCH Jurisdictional Survey Instrument for the Title V MCH Block Grant Program, OMB No. 0906-0042, Extension, 50365-50367 [2021-19447]

Download as PDF Federal Register / Vol. 86, No. 171 / Wednesday, September 8, 2021 / Notices jbell on DSKJLSW7X2PROD with NOTICES In addition, for evaluation of novel excipients with a proposed use in formulations for biological drug products reviewed by CDER/OND, submitters should provide: • Stability studies of the excipient under storage and potential in-use conditions (e.g., over infusion time). Novel excipients should be evaluated for their potential to prevent denaturation and degradation of proteins during storage. • For some excipients, studies should address their potential protein-excipient interaction and impact on drug product immunogenicity as well as their potential for masking process related impurities. Full packages should be submitted through a Type V DMF or other master file no later than 3 months after notification that FDA has selected the proposal. For more information on submitting Type V DMFs, see the FDA draft guidance for industry entitled ‘‘Drug Master Files’’ (Ref. 8). FDA will evaluate the full package and determine whether the excipient is appropriate for the proposed use for use in clinical trials. FDA will issue a letter to the novel excipient submitter announcing its decision. For each novel excipient evaluated under the second stage of the program, FDA will publish on the Pilot Program web page the initial proposal and the determination letter. Information that cannot be publicly disclosed will be redacted. This web page will also include a content outline identifying information that should be included in an Initial Proposal and other relevant information regarding the pilot. 3. Effect of Determination A determination that the excipient is appropriate for use in clinical trials means that FDA has determined it is appropriate to use the novel excipient in an IND within the defined use without additional justification. However, the drug sponsor would still need to demonstrate that the excipient is safe in the proposed formulation. The information submitted under the full package would remain in the Type V DMF or other master file, and the master file holder may grant authorization to reference the information in the master file at the holder’s discretion. Moreover, we do not anticipate that a novel excipient may be used in an abbreviated new drug application because data and information currently required to support use of a novel excipient may not be submitted in an abbreviated new drug application. After it has been used in approved drug products, the novel excipient would be added to the VerDate Sep<11>2014 17:21 Sep 07, 2021 Jkt 253001 Inactive Ingredient Database in accordance with Agency practice. If FDA determines that the excipient is not appropriate for the proposed use, an IND sponsor would be expected to provide additional information to demonstrate that the use of the novel excipient is appropriate within the context of the IND. II. Paperwork Reduction Act of 1995 The information collection activities associated with the Pilot Program refer to previously approved FDA collections of information. Therefore, clearance by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995 (PRA) (44 U.S.C. 3501– 3521) is not required for this Pilot Program. The previously approved collections of information are subject to review by OMB under the PRA. The collections of information in 21 CFR part 314 pertaining to the submission of abbreviated new drug applications, new drug applications, and DMFs have been approved under OMB control number 0910–0001. The collections of information in 21 CFR part 312 pertaining to the submission of IND content and format; chemistry, control, and manufacturing data; pharmacology and toxicology data; and pharmacokinetics and biological data have been approved under OMB control number 0910–0014. The collections of information in 21 CFR part 58 pertaining to good laboratory practice regulations for nonclinical laboratory studies have been approved under OMB control number 0910–0119. The collections of information in 21 CFR part 601 pertaining to biologics license applications have been approved under OMB control number 0910–0338. III. References The following references are on display at the Dockets Management Staff (HFA–305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852, 240–402– 7500, and are available for viewing by interested persons between 9 a.m. and 4 p.m., Monday through Friday; they are also available electronically at https:// www.regulations.gov. FDA has verified the website addresses, as of the date this document publishes in the Federal Register, but websites are subject to change over time. 1. FDA, Guidance for Industry, ‘‘Nonclinical Studies for the Safety Evaluation of Pharmaceutical Excipients,’’ May 2005 (available at https://www.fda.gov/media/ 72260/download). For the most recent version of a guidance, check the FDA guidance web page at https:// www.fda.gov/regulatory-information/ PO 00000 Frm 00043 Fmt 4703 Sfmt 4703 50365 search-fda-guidance-documents. 2. FDA Guidance for Industry, ‘‘S7A Safety Pharmacology Studies for Human Pharmaceuticals,’’ July 2001 (available at https://www.fda.gov/media/72033/ download). 3. FDA, Guidance for Industry, ‘‘M3(R2) Nonclinical Safety Studies for the Conduct of Human Clinical Trials and Marketing Authorization for Pharmaceuticals,’’ January 2010 (available at https://www.fda.gov/media/ 71542/download). 4. FDA, Guidance for Industry, ‘‘S2B Genotoxicity: A Standard Battery for Genotoxicity Testing of Pharmaceuticals,’’ July 1997 (available at https://www.fda.gov/media/71971/ download). 5. International Council for Harmonization (ICH), Guidance for Industry, ‘‘Detection of Reproductive and Developmental Toxicity for Human Pharmaceuticals S5(R3),’’ February 2020 (available at https://database.ich.org/sites/default/ files/S5-R3_Step4_Guideline_2020_ 0218_1.pdf). 6. FDA, Guidance for Industry, ‘‘The Need for Long-term Rodent Carcinogenicity Studies of Pharmaceuticals,’’ March 1996 (available at https://www.fda.gov/media/ 71921/download). 7. FDA, Guidance for Industry, ‘‘S8 Immunotoxicity Studies for Human Pharmaceuticals,’’ April 2006 (available at https://www.fda.gov/media/72047/ download). 8. FDA, Draft Guidance for Industry ‘‘Drug Master Files,’’ October 2019 (available at https://www.fda.gov/media/131861/ download). Dated: September 1, 2021. Lauren K. Roth, Acting Principal Associate Commissioner for Policy. [FR Doc. 2021–19335 Filed 9–7–21; 8:45 am] BILLING CODE 4164–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Health Resources and Services Administration Agency Information Collection Activities: Proposed Collection: Public Comment Request; Information Collection Request Title: MCH Jurisdictional Survey Instrument for the Title V MCH Block Grant Program, OMB No. 0906–0042, Extension Health Resources and Services Administration (HRSA), Department of Health and Human Services. ACTION: Notice. AGENCY: In compliance with the requirement of the Paperwork Reduction Act of 1995 for opportunity for public comment on proposed data collection projects, HRSA announces SUMMARY: E:\FR\FM\08SEN1.SGM 08SEN1 50366 Federal Register / Vol. 86, No. 171 / Wednesday, September 8, 2021 / Notices jbell on DSKJLSW7X2PROD with NOTICES plans to submit an Information Collection Request (ICR), described below, to the Office of Management and Budget (OMB). Prior to submitting the ICR to OMB, HRSA seeks comments from the public regarding the burden estimate, or any other aspect of the ICR related to the Maternal and Child Health (MCH) Jurisdictional Survey that is to be administered in the U.S. territories and jurisdictions (excluding the District of Columbia) for purposes of collecting information related to the well-being of all mothers, children, and their families. DATES: Comments on this Information Collection Request must be received no later than November 8, 2021. ADDRESSES: Submit your comments to paperwork@hrsa.gov or by mail to the HRSA Information Collection Clearance Officer, Room 14N136B, 5600 Fishers Lane, Rockville, MD 20857. FOR FURTHER INFORMATION CONTACT: To request more information on the proposed project or to obtain a copy of the data collection plans and draft instruments, email paperwork@hrsa.gov or call the HRSA Information Collection Clearance Officer at (301) 443–1984. SUPPLEMENTARY INFORMATION: When submitting comments or requesting information, please include the information request collection title for reference. Information Collection Request Title: MCH Jurisdictional Survey Instrument for the Title V MCH Block Grant Program, OMB No. 0906–0042, Extension. Abstract: The purpose of the Title V MCH Block Grant is to improve the health of the nation’s mothers, infants, children, including children with special health care needs, and their families by creating federal/state partnerships that provide each state/ jurisdiction with needed flexibility to respond to its individual MCH population needs. Unique to the MCH Block Grant is a commitment to performance accountability, while assuring state flexibility. Utilizing a three-tiered national performance measure framework, which includes National Outcome Measures, National Performance Measures, and EvidenceBased and Informed Strategy Measures, State Title V programs report annually on their performance relative to the selected national performance and outcome measures. Such reporting VerDate Sep<11>2014 17:21 Sep 07, 2021 Jkt 253001 enables the state and federal program offices to assess the progress achieved in key MCH priority areas and to document Title V program accomplishments. By legislation (Sections 505(a) and 506(a) of Title V of the Social Security Act), the MCH Block Grant Application/ Annual Report must be developed by, or in consultation with, the State MCH Health agency. In establishing state reporting requirements, HRSA’s Maternal and Child Health Bureau considers the availability of national data from other federal agencies. Data for the national performance and outcome measures are pre-populated for states in the Title V Information System. National data sources identified for the National Performance Measures and National Outcome Measures in the MCH Block Grant program seldom include data from the Title V jurisdictions, with the exception of the District of Columbia. The eight remaining jurisdictions (i.e., American Samoa, Federated States of Micronesia, Guam, Marshall Islands, Northern Mariana Islands, Palau, Puerto Rico and U.S. Virgin Islands) have limited access to significant data and MCH indicators, with limited capacity for collecting these data. Sponsored by HRSA’s Maternal and Child Health Bureau, the MCH Jurisdictional Survey is designed to produce data on the physical and emotional health of mothers and children under 18 years of age in the following eight jurisdictions—American Samoa, Federated States of Micronesia, Guam, Marshall Islands, Northern Mariana Islands, Palau, Puerto Rico, and Virgin Islands. More specifically, the MCH Jurisdictional Survey collects information on factors related to the well-being of children, including health status, visits to health care providers, health care costs, and health insurance coverage. In addition, the MCH Jurisdictional Survey collects information on factors related to the well-being of mothers, including health risk behaviors, health conditions, and preventive health practices. This data collection enables the jurisdictions to meet federal performance reporting requirements and to demonstrate the impact of Title V funding relative to MCH outcomes for the U.S. jurisdictions in reporting on their unique MCH priority needs. PO 00000 Frm 00044 Fmt 4703 Sfmt 4703 The MCH Jurisdictional Survey was designed based on informationgathering activities with Title V leadership and program staff in the jurisdictions, experts at the Centers for Disease Control and Prevention and other organizations with relevant data collection experience. Survey items are based on the National Survey of Children’s Health; the Behavioral Risk Factor Surveillance System; the Youth Behavior Surveillance System; and selected other federal studies. The Survey is designed as a core questionnaire to be administered across all jurisdictions with a supplemental set of survey questions customized to the needs of each jurisdiction. Need and Proposed Use of the Information: Data from the MCH Jurisdictional Survey is used to measure progress on national performance and outcome measures under the Title V MCH Block Grant Program. This survey instrument is critical to collect information on factors related to the well-being of all mothers, children, and their families in the jurisdictional Title V programs, which address their unique MCH needs. Likely Respondents: The respondent universe is women age 18 or older who live in one of the eight targeted U.S. jurisdictions (Puerto Rico, U.S. Virgin Islands, Guam, Northern Mariana Islands, American Samoa, Palau, Marshall Islands, or Federated States of Micronesia) and who are mothers or guardians of at least one child aged 0–17 years living in the same household. Burden Statement: Burden in this context means the time expended by persons to generate, maintain, retain, disclose, or provide the information requested. Included is the time needed to review instructions; to develop, acquire, install, and utilize technology and systems for the purpose of collecting, validating and verifying information, processing and maintaining information, and disclosing and providing information; to train personnel and to be able to respond to a collection of information; to search data sources; to complete and review the collection of information; and to transmit or otherwise disclose the information. The total annual burden hours estimated for this ICR are summarized in the table below. E:\FR\FM\08SEN1.SGM 08SEN1 50367 Federal Register / Vol. 86, No. 171 / Wednesday, September 8, 2021 / Notices TOTAL ESTIMATED ANNUALIZED BURDEN HOURS Adult Parents—Puerto Rico .. Screener ................................ Core ....................................... Jurisdiction Module ............... 2,480 250 250 1 1 1 2,480 250 250 0.03 0.83 0.07 74.40 207.50 17.50 299.40 Adult Parents—U.S. Virgin Islands. Screener ................................ Core ....................................... Jurisdiction Module ............... 2,153 250 250 1 1 1 2,153 250 250 0.03 0.83 0.07 64.59 207.50 17.50 289.59 Adult Parents—Guam ........... Screener ................................ Core ....................................... Jurisdiction Module ............... 684 250 250 1 1 1 684 250 250 0.03 0.83 0.07 20.52 207.50 17.50 245.52 Adult Parents—American Samoa. Screener ................................ Core ....................................... Jurisdiction Module ............... 426 250 250 1 1 1 426 250 250 0.03 0.83 0.05 12.78 207.50 12.50 232.78 Adult Parents—Federated States of Micronesia. Screener ................................ Core ....................................... Jurisdiction Module ............... 339 250 250 1 1 1 339 250 250 0.03 0.83 0.05 10.17 207.50 12.50 230.17 Adult Parents—Marshall Islands. Screener ................................ Core ....................................... Jurisdiction Module ............... 284 250 250 1 1 1 284 250 250 0.03 0.83 0.08 8.52 207.50 20.00 236.02 Adult Parents—Northern Mariana Islands. Screener ................................ Core ....................................... Jurisdiction Module ............... 470 250 250 1 1 1 470 250 250 0.03 0.83 0.08 14.10 207.50 20.00 241.60 Adult Parents—Palau ............ Screener ................................ Core ....................................... Jurisdiction Module ............... 467 250 250 1 1 1 467 250 250 0.03 0.83 0.02 14.01 207.50 5.00 226.51 Total ............................... ................................................ 7,303 ........................ 7,303 ........................ ........................ 2,001.59 Maria G. Button, Director, Executive Secretariat. [FR Doc. 2021–19447 Filed 9–7–21; 8:45 am] BILLING CODE 4165–15–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health jbell on DSKJLSW7X2PROD with NOTICES Average burden per response (in hours) Form name HRSA specifically requests comments on (1) the necessity and utility of the proposed information collection for the proper performance of the agency’s functions, (2) the accuracy of the estimated burden, (3) ways to enhance the quality, utility, and clarity of the information to be collected, and (4) the use of automated collection techniques or other forms of information technology to minimize the information collection burden. Submission for OMB Review; 30-Day Comment Request; Evaluation of Office of Acquisitions System (OASYS) and FFRDC Contract Administration System (FCAS) Vendor Portals National Cancer Institute (NCI); Correction AGENCY: National Institutes of Health, HHS. ACTION: Notice; correction. VerDate Sep<11>2014 17:21 Sep 07, 2021 Jkt 253001 Number of respondents Number of responses per respondent Type of respondent Total responses The Department of Health and Human Services, National Institutes of Health published a Notice in the Federal Register on August 31, 2021. That Notice requires a correction in the SUPPLEMENTARY INFORMATION section. 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. FOR FURTHER INFORMATION CONTACT: Marla Jacobson, 9609 Medical Center Drive, MSC 9742, Rockville, MD 20850 or call non-toll-free number 240–276– 5267 or email your request, including your address to: marla.jacobson@ nih.gov. Formal requests for additional plans and instruments must be requested in writing. SUPPLEMENTARY INFORMATION: SUMMARY: Correction In the Federal Register of August 31, 2021, in FR Doc. 2021–18767, on page 48747, as found within the SUPPLEMENTARY INFORMATION section, within the Estimated Annualized Burden Hours table for the Total Annual PO 00000 Frm 00045 Fmt 4703 Sfmt 4703 Burden hours per form Total burden hours Burden Hours for the form name column Survey—FCAS total currently reads ‘‘1’’ and is corrected to read: ‘‘0’’, the form name column Registration— FCAS total currently reads ‘‘1’’ and is corrected to read: ‘‘0’’. These corrections revise the Total Annual Burden Hours total currently reads ‘‘232’’ and is corrected to read: ‘‘230’’. Dated: September 1, 2021. Diane Kreinbrink, Project Clearance Liaison, National Cancer Institute, National Institutes of Health. [FR Doc. 2021–19281 Filed 9–7–21; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Institute on Minority Health and Health Disparities; Notice of Closed Meetings Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended, notice is hereby given of the following meetings. The meetings will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. The grant applications and E:\FR\FM\08SEN1.SGM 08SEN1

Agencies

[Federal Register Volume 86, Number 171 (Wednesday, September 8, 2021)]
[Notices]
[Pages 50365-50367]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-19447]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Health Resources and Services Administration


Agency Information Collection Activities: Proposed Collection: 
Public Comment Request; Information Collection Request Title: MCH 
Jurisdictional Survey Instrument for the Title V MCH Block Grant 
Program, OMB No. 0906-0042, Extension

AGENCY: Health Resources and Services Administration (HRSA), Department 
of Health and Human Services.

ACTION: Notice.

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

SUMMARY: In compliance with the requirement of the Paperwork Reduction 
Act of 1995 for opportunity for public comment on proposed data 
collection projects, HRSA announces

[[Page 50366]]

plans to submit an Information Collection Request (ICR), described 
below, to the Office of Management and Budget (OMB). Prior to 
submitting the ICR to OMB, HRSA seeks comments from the public 
regarding the burden estimate, or any other aspect of the ICR related 
to the Maternal and Child Health (MCH) Jurisdictional Survey that is to 
be administered in the U.S. territories and jurisdictions (excluding 
the District of Columbia) for purposes of collecting information 
related to the well-being of all mothers, children, and their families.

DATES: Comments on this Information Collection Request must be received 
no later than November 8, 2021.

ADDRESSES: Submit your comments to [email protected] or by mail to the 
HRSA Information Collection Clearance Officer, Room 14N136B, 5600 
Fishers Lane, Rockville, MD 20857.

FOR FURTHER INFORMATION CONTACT: To request more information on the 
proposed project or to obtain a copy of the data collection plans and 
draft instruments, email [email protected] or call the HRSA 
Information Collection Clearance Officer at (301) 443-1984.

SUPPLEMENTARY INFORMATION: When submitting comments or requesting 
information, please include the information request collection title 
for reference.
    Information Collection Request Title: MCH Jurisdictional Survey 
Instrument for the Title V MCH Block Grant Program, OMB No. 0906-0042, 
Extension.
    Abstract: The purpose of the Title V MCH Block Grant is to improve 
the health of the nation's mothers, infants, children, including 
children with special health care needs, and their families by creating 
federal/state partnerships that provide each state/jurisdiction with 
needed flexibility to respond to its individual MCH population needs. 
Unique to the MCH Block Grant is a commitment to performance 
accountability, while assuring state flexibility. Utilizing a three-
tiered national performance measure framework, which includes National 
Outcome Measures, National Performance Measures, and Evidence-Based and 
Informed Strategy Measures, State Title V programs report annually on 
their performance relative to the selected national performance and 
outcome measures. Such reporting enables the state and federal program 
offices to assess the progress achieved in key MCH priority areas and 
to document Title V program accomplishments.
    By legislation (Sections 505(a) and 506(a) of Title V of the Social 
Security Act), the MCH Block Grant Application/Annual Report must be 
developed by, or in consultation with, the State MCH Health agency. In 
establishing state reporting requirements, HRSA's Maternal and Child 
Health Bureau considers the availability of national data from other 
federal agencies. Data for the national performance and outcome 
measures are pre-populated for states in the Title V Information 
System. National data sources identified for the National Performance 
Measures and National Outcome Measures in the MCH Block Grant program 
seldom include data from the Title V jurisdictions, with the exception 
of the District of Columbia. The eight remaining jurisdictions (i.e., 
American Samoa, Federated States of Micronesia, Guam, Marshall Islands, 
Northern Mariana Islands, Palau, Puerto Rico and U.S. Virgin Islands) 
have limited access to significant data and MCH indicators, with 
limited capacity for collecting these data.
    Sponsored by HRSA's Maternal and Child Health Bureau, the MCH 
Jurisdictional Survey is designed to produce data on the physical and 
emotional health of mothers and children under 18 years of age in the 
following eight jurisdictions--American Samoa, Federated States of 
Micronesia, Guam, Marshall Islands, Northern Mariana Islands, Palau, 
Puerto Rico, and Virgin Islands. More specifically, the MCH 
Jurisdictional Survey collects information on factors related to the 
well-being of children, including health status, visits to health care 
providers, health care costs, and health insurance coverage. In 
addition, the MCH Jurisdictional Survey collects information on factors 
related to the well-being of mothers, including health risk behaviors, 
health conditions, and preventive health practices. This data 
collection enables the jurisdictions to meet federal performance 
reporting requirements and to demonstrate the impact of Title V funding 
relative to MCH outcomes for the U.S. jurisdictions in reporting on 
their unique MCH priority needs.
    The MCH Jurisdictional Survey was designed based on information-
gathering activities with Title V leadership and program staff in the 
jurisdictions, experts at the Centers for Disease Control and 
Prevention and other organizations with relevant data collection 
experience. Survey items are based on the National Survey of Children's 
Health; the Behavioral Risk Factor Surveillance System; the Youth 
Behavior Surveillance System; and selected other federal studies. The 
Survey is designed as a core questionnaire to be administered across 
all jurisdictions with a supplemental set of survey questions 
customized to the needs of each jurisdiction.
    Need and Proposed Use of the Information: Data from the MCH 
Jurisdictional Survey is used to measure progress on national 
performance and outcome measures under the Title V MCH Block Grant 
Program. This survey instrument is critical to collect information on 
factors related to the well-being of all mothers, children, and their 
families in the jurisdictional Title V programs, which address their 
unique MCH needs.
    Likely Respondents: The respondent universe is women age 18 or 
older who live in one of the eight targeted U.S. jurisdictions (Puerto 
Rico, U.S. Virgin Islands, Guam, Northern Mariana Islands, American 
Samoa, Palau, Marshall Islands, or Federated States of Micronesia) and 
who are mothers or guardians of at least one child aged 0-17 years 
living in the same household.
    Burden Statement: Burden in this context means the time expended by 
persons to generate, maintain, retain, disclose, or provide the 
information requested. Included is the time needed to review 
instructions; to develop, acquire, install, and utilize technology and 
systems for the purpose of collecting, validating and verifying 
information, processing and maintaining information, and disclosing and 
providing information; to train personnel and to be able to respond to 
a collection of information; to search data sources; to complete and 
review the collection of information; and to transmit or otherwise 
disclose the information. The total annual burden hours estimated for 
this ICR are summarized in the table below.

[[Page 50367]]



                                                         Total Estimated Annualized Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
                                                                             Number of                    Average burden
        Type of respondent                Form name          Number of     responses per       Total       per response    Burden hours    Total burden
                                                            respondents     respondent       responses      (in hours)       per form          hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Adult Parents--Puerto Rico........  Screener............           2,480               1           2,480            0.03           74.40          299.40
                                    Core................             250               1             250            0.83          207.50
                                    Jurisdiction Module.             250               1             250            0.07           17.50
--------------------------------------------------------------------------------------------------------------------------------------------------------
Adult Parents--U.S. Virgin Islands  Screener............           2,153               1           2,153            0.03           64.59          289.59
                                    Core................             250               1             250            0.83          207.50
                                    Jurisdiction Module.             250               1             250            0.07           17.50
--------------------------------------------------------------------------------------------------------------------------------------------------------
Adult Parents--Guam...............  Screener............             684               1             684            0.03           20.52          245.52
                                    Core................             250               1             250            0.83          207.50
                                    Jurisdiction Module.             250               1             250            0.07           17.50
--------------------------------------------------------------------------------------------------------------------------------------------------------
Adult Parents--American Samoa.....  Screener............             426               1             426            0.03           12.78          232.78
                                    Core................             250               1             250            0.83          207.50
                                    Jurisdiction Module.             250               1             250            0.05           12.50
--------------------------------------------------------------------------------------------------------------------------------------------------------
Adult Parents--Federated States of  Screener............             339               1             339            0.03           10.17          230.17
 Micronesia.                        Core................             250               1             250            0.83          207.50
                                    Jurisdiction Module.             250               1             250            0.05           12.50
--------------------------------------------------------------------------------------------------------------------------------------------------------
Adult Parents--Marshall Islands...  Screener............             284               1             284            0.03            8.52          236.02
                                    Core................             250               1             250            0.83          207.50
                                    Jurisdiction Module.             250               1             250            0.08           20.00
--------------------------------------------------------------------------------------------------------------------------------------------------------
Adult Parents--Northern Mariana     Screener............             470               1             470            0.03           14.10          241.60
 Islands.                           Core................             250               1             250            0.83          207.50
                                    Jurisdiction Module.             250               1             250            0.08           20.00
--------------------------------------------------------------------------------------------------------------------------------------------------------
Adult Parents--Palau..............  Screener............             467               1             467            0.03           14.01          226.51
                                    Core................             250               1             250            0.83          207.50
                                    Jurisdiction Module.             250               1             250            0.02            5.00
--------------------------------------------------------------------------------------------------------------------------------------------------------
    Total.........................  ....................           7,303  ..............           7,303  ..............  ..............        2,001.59
--------------------------------------------------------------------------------------------------------------------------------------------------------

    HRSA specifically requests comments on (1) the necessity and 
utility of the proposed information collection for the proper 
performance of the agency's functions, (2) the accuracy of the 
estimated burden, (3) ways to enhance the quality, utility, and clarity 
of the information to be collected, and (4) the use of automated 
collection techniques or other forms of information technology to 
minimize the information collection burden.

Maria G. Button,
Director, Executive Secretariat.
[FR Doc. 2021-19447 Filed 9-7-21; 8:45 am]
BILLING CODE 4165-15-P