Agency Information Collection Request; 60-Day Public Comment Request, 54695-54696 [2021-21560]
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54695
Federal Register / Vol. 86, No. 189 / Monday, October 4, 2021 / Notices
their parents and asked if they wish to
provide informed consent for
participation in surveys.
CDC requests OMB approval for an
estimated 6,193 annual burden hours.
There are no costs to respondents other
than their time to participate.
reported symptoms of anxiety,
depression, quality of life, social
camouflaging, gender identity,
sexuality, and relationships). Children
who originally participated at age 2–5
years, who are now adolescents and
young adults, will be contacted through
participated in SEED because it is the
parents who provided consent for
follow-up studies. However, many
emerging issues surrounding the
transition to adulthood among
adolescents with ASD require self,
rather than parental report (e.g., self-
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Number of
respondents
Average
burden per
response
(in hours)
Total burden
hours
Type of respondents
Form name
Parent ................................................
Review of invitation letter and call
script for first follow-up survey.
First follow-up core survey of SEED
1–3 parents.
First follow-up survey supplement
for parents of children.
First follow-up survey supplement
for parents of adolescents.
First follow-up survey supplement
for parents of adults.
Second follow-up survey of SEED 1
parents.
Invitation and informed consent
script.
Second follow-up survey of SEED 1
adult children.
Parents or adult children receiving
informed consent or assent script.
In-person assessment of intellectual
abilities.
5,850
1
10/60
975
3,900
1
40/60
2,600
1,300
1
20/60
433
1,300
1
20/60
433
1,300
1
20/60
433
1,105
1
10/60
184
520
1
10/60
87
520
1
30/60
260
472
1
10/60
79
472
1
90/60
708
...........................................................
........................
........................
........................
6,193
Parent ................................................
Parent ................................................
Parent ................................................
Parent ................................................
Parent ................................................
Adult Child .........................................
Adult Child .........................................
Children age 8–22 years or their
parents.
Children age 8–22 years ..................
Total ...........................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2021–21524 Filed 10–1–21; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[Document Identifier: OS–4040–0014]
Agency Information Collection
Request; 60-Day Public Comment
Request
Office of the Secretary, HHS.
Notice.
AGENCY:
ACTION:
In compliance with the
requirement of the Paperwork
Reduction Act of 1995, the Office of the
Secretary (OS), Department of Health
and Human Services, is publishing the
following summary of a proposed
collection for public comment.
DATES: Comments on the ICR must be
received on or before December 3, 2021.
SUMMARY:
VerDate Sep<11>2014
22:52 Oct 01, 2021
Jkt 256001
Submit your comments to
sagal.musa@hhs.gov or by calling (202)
205–2634.
FOR FURTHER INFORMATION CONTACT:
When submitting comments or
requesting information, please include
the document identifier 4040–0014–
NEW–60D and project title for reference,
to Sagal Musa, email:
sagal.musa@hhs.gov, or call (202) 205–
2634 the Reports Clearance Officer.
SUPPLEMENTARY INFORMATION: Interested
persons are invited to send comments
regarding this burden estimate or any
other aspect of this collection of
information, including any of the
following subjects: (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.
Title of the Collection: Federal
Financial Report (SF–425) and Federal
ADDRESSES:
PO 00000
Frm 00023
Fmt 4703
Sfmt 4703
Financial Report Attachment (SF–
425A).
Type of Collection: Renewal.
OMB No. 4040–0014.
Abstract
Abstract: Federal Financial Report
(SF–425) and Federal Financial Report
Attachment (SF–425A) are used by
applicants to apply for Federal financial
assistance. The Federal Financial Report
(SF–425) and Federal Financial Report
Attachment (SF–425A) forms allow the
applicants to provide certain financial
information as part of their grant
proposals. These forms are evaluated by
Federal agencies as part of the overall
grant application. This IC expires on
February 28, 2022. Grants.gov seeks a
three-year clearance of these collections.
Type of Respondent: The Federal
Financial Report (SF–425) and Federal
Financial Report Attachment (SF–425A)
forms are used by organizations to apply
for Federal financial assistance in the
form of grants. These forms are
submitted to the Federal grant-making
agencies for evaluation and review.
E:\FR\FM\04OCN1.SGM
04OCN1
54696
Federal Register / Vol. 86, No. 189 / Monday, October 4, 2021 / Notices
ANNUALIZED BURDEN HOUR TABLE
Number of
responses per
respondents
Average
burden per
response
Forms
(if necessary)
Respondents
(if necessary)
Number of
respondents
Federal Financial Report (SF–
425) and Federal Financial Report Attachment (SF–425A).
Grant-seeking organizations .......
100,000 .....................
1
1
100,000
Grant-seeking organizations .......
100,000 .....................
1
1
100,000
.....................................................
...................................
1
........................
200,000
Total .....................................
Sherrette A. Funn,
Paperwork Reduction Act Reports Clearance
Officer, Office of the Secretary.
Services, 200 Independence Avenue
SW, Washington, DC 20201; 202–260–
0365, paige.ezernack@hhs.gov.
[FR Doc. 2021–21560 Filed 10–1–21; 8:45 am]
Corrections
Corrections to technical errors that
appeared in sections V(d) and (h) and
XII of the final notice published in the
Federal Register on September 14, 2021
at 86 FR 51160 entitled ‘‘Ninth
Amendment to Declaration Under the
Public Readiness and Emergency
Preparedness Act for Medical
Countermeasures Against COVID–19.
These corrections are made to clarify
that when the term Advisory Committee
on Immunization Practices (ACIP)
schedule or recommendation is used in
the declaration, that refers to
recommendations made to the Centers
for Disease Control and Prevention
(CDC) by the ACIP in its advisory role
under the Federal Advisory Committee
Act. Such recommendations are taken
into consideration when the CDC issues
its recommendations, as adopted by the
CDC Director. These have historically
been published in CDC’s Morbidity and
Mortality Weekly Report under the title
‘‘ACIP recommendations.’’ The term
‘‘CDC’’ is added throughout the
declaration whenever referring to ACIP
recommendations or schedules to also
recognizes coverage of
recommendations issued directly by the
CDC. Subsection V(d) is clarified to
read:
(d) A State-licensed pharmacist who
orders and administers, and pharmacy
interns and qualified pharmacy
technicians who administer (if the
pharmacy intern or technician acts
under the supervision of such
pharmacist and the pharmacy intern or
technician is licensed or registered by
his or her State board of pharmacy),1 (1)
BILLING CODE 4151–AE–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
Declaration Under the Public
Readiness and Emergency
Preparedness Act for Medical
Countermeasures Against COVID–19;
Correction
ACTION:
Notice, correction.
This document clarifies a
term that appeared in the ‘‘Declaration
Under the Public Readiness and
Emergency Preparedness Act for
Medical Countermeasures Against
COVID–19,’’ including in the final
notice published in the Federal Register
on September 14, 2021, entitled ‘‘Ninth
Amendment to Declaration Under the
Public Readiness and Emergency
Preparedness Act for Medical
Countermeasures Against COVID–19.’’
Specifically, this document
supplements the references to the
Advisory Committee on Immunization
Practices (ACIP) with references to the
Centers for Disease Control and
Prevention (CDC). This change is being
made to clarify that what are commonly
referred to as ‘‘ACIP recommendations’’
and ‘‘ACIP standard immunization
schedules’’ are in fact recommendations
and schedules made by the CDC after
consultation with ACIP. The addition of
‘‘CDC’’ is also intended to recognize
coverage of recommendations issued
directly by the CDC. This clarification
also applies to related guidance and
opinions.
DATES: This correction is applicable
September 30, 2021.
FOR FURTHER INFORMATION CONTACT: L.
Paige Ezernack, Office of the Assistant
Secretary for Preparedness and
Response, Office of the Secretary,
Department of Health and Human
SUMMARY:
VerDate Sep<11>2014
22:52 Oct 01, 2021
Jkt 256001
1 Some states do not require pharmacy interns to
be licensed or registered by the state board of
pharmacy. As used herein, ‘‘State-licensed or
registered intern’’ (or equivalent phrases) refers to
pharmacy interns authorized by the state or board
of pharmacy in the state in which the practical
pharmacy internship occurs. The authorization can,
but need not, take the form of a license from, or
registration with, the State board of pharmacy.
Similarly, states vary on licensure and registration
requirements for pharmacy technicians. Some states
PO 00000
Frm 00024
Fmt 4703
Sfmt 4703
Total burden
hours
Vaccines that the CDC/ACIP
recommend 2 to persons ages three
through 18 according to CDC’s/ACIP’s
standard immunization schedule or (2)
seasonal influenza vaccine administered
by qualified pharmacy technicians and
interns that the CDC/ACIP recommend
to persons aged 19 and older according
to CDC’s/ACIP’s standard immunization
schedule; or (3) FDA authorized or FDA
licensed COVID–19 vaccines to persons
ages three or older. Such State-licensed
pharmacists and the State-licensed or
registered interns or technicians under
their supervision are qualified persons
only if the following requirements are
met:
i. The vaccine must be authorized,
approved, or licensed by the FDA;
ii. In the case of a COVID–19 vaccine,
the vaccination must be ordered and
administered according to CDC’s/ACIP’s
COVID–19 vaccine recommendation(s);
iii. In the case of a childhood vaccine,
the vaccination must be ordered and
administered according to CDC’s/ACIP’s
standard immunization schedule;
iv. In the case of seasonal influenza
vaccine administered by qualified
pharmacy technicians and interns, the
vaccination must be ordered and
require certain education, training, and/or
certification for licensure or registration; others
either have no prerequisites for licensure or
registration or do not require licensure or
registration at all. As used herein, to be a ‘‘qualified
pharmacy technician,’’ pharmacy technicians
working in states with licensure and/or registration
requirements must be licensed and/or registered in
accordance with state requirements; pharmacy
technicians working in states without licensure
and/or registration requirements must have a CPhT
certification from either the Pharmacy Technician
Certification Board or National Healthcareer
Association. See Guidance for PREP Act Coverage
for Qualified Pharmacy Technicians and StateAuthorized Pharmacy Interns for Childhood
Vaccines, COVID–19 Vaccines, and COVID–19
Testing, OASH, Oct. 20, 2020 at 2, available at
https://www.hhs.gov/guidance/sites/default/files/
hhs-guidance-documents//prep-act-guidance.pdf
(last visited Jan. 24, 2021).
2 Where the term CDC/ACIP recommendations,
standard immunization schedules, or similar
language is used, this includes both direct CDC
recommendations as well as recommendations
adopted by the CDC Director after recommendation
by ACIP, which are commonly referred to as ACIP
recommendations or schedules.
E:\FR\FM\04OCN1.SGM
04OCN1
]]>Agencies
[Federal Register Volume 86, Number 189 (Monday, October 4, 2021)]
[Notices]
[Pages 54695-54696]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-21560]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
[Document Identifier: OS-4040-0014]
Agency Information Collection Request; 60-Day Public Comment
Request
AGENCY: Office of the Secretary, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with the requirement of the Paperwork Reduction
Act of 1995, the Office of the Secretary (OS), Department of Health and
Human Services, is publishing the following summary of a proposed
collection for public comment.
DATES: Comments on the ICR must be received on or before December 3,
2021.
ADDRESSES: Submit your comments to [email protected] or by calling
(202) 205-2634.
FOR FURTHER INFORMATION CONTACT: When submitting comments or requesting
information, please include the document identifier 4040-0014-NEW-60D
and project title for reference, to Sagal Musa, email:
[email protected], or call (202) 205-2634 the Reports Clearance
Officer.
SUPPLEMENTARY INFORMATION: Interested persons are invited to send
comments regarding this burden estimate or any other aspect of this
collection of information, including any of the following subjects: (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.
Title of the Collection: Federal Financial Report (SF-425) and
Federal Financial Report Attachment (SF-425A).
Type of Collection: Renewal.
OMB No. 4040-0014.
Abstract
Abstract: Federal Financial Report (SF-425) and Federal Financial
Report Attachment (SF-425A) are used by applicants to apply for Federal
financial assistance. The Federal Financial Report (SF-425) and Federal
Financial Report Attachment (SF-425A) forms allow the applicants to
provide certain financial information as part of their grant proposals.
These forms are evaluated by Federal agencies as part of the overall
grant application. This IC expires on February 28, 2022. Grants.gov
seeks a three-year clearance of these collections.
Type of Respondent: The Federal Financial Report (SF-425) and
Federal Financial Report Attachment (SF-425A) forms are used by
organizations to apply for Federal financial assistance in the form of
grants. These forms are submitted to the Federal grant-making agencies
for evaluation and review.
[[Page 54696]]
Annualized Burden Hour Table
----------------------------------------------------------------------------------------------------------------
Number of
Forms (if necessary) Respondents (if Number of responses per Average burden Total burden
necessary) respondents respondents per response hours
----------------------------------------------------------------------------------------------------------------
Federal Financial Report (SF- Grant-seeking 100,000........ 1 1 100,000
425) and Federal Financial organizations.
Report Attachment (SF-425A).
Grant-seeking 100,000........ 1 1 100,000
organizations.
----------------------------------------------------------------
Total.................... ................ ............... 1 .............. 200,000
----------------------------------------------------------------------------------------------------------------
Sherrette A. Funn,
Paperwork Reduction Act Reports Clearance Officer, Office of the
Secretary.
[FR Doc. 2021-21560 Filed 10-1-21; 8:45 am]
BILLING CODE 4151-AE-P
