Pathogen Reduction Technologies for Blood Safety; Public Workshop; Correction, 51961 [2018-22364]
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Federal Register / Vol. 83, No. 199 / Monday, October 15, 2018 / Notices
3. first name.
4. date of birth.
The data elements the AEs will
receive from CMS may include:
1. Validation of SSN.
2. verification of citizenship or
immigration status.
3. incarceration status.
4. eligibility and/or enrollment in
certain types of minimum essential
coverage.
5. income, based on federal tax
information (FTI), Title II benefits, and
current income sources.
6. quarters of coverage.
7. death indicator.
System(s) of Records
The records that CMS will disclose to
AEs will be disclosed from the
following systems of records, as
authorized by routine use 3 published
in the System of Records Notices
(SORNs ) cited below:
• CMS Health Insurance Exchanges
System (HIX), CMS System No. 09–70–
0560, last published in full at 78 FR
63211 (Oct. 23, 2013), as amended at 83
FR 6591 (Feb. 14, 2018).
[FR Doc. 2018–22405 Filed 10–12–18; 8:45 am]
In the
Federal Register of Monday, September
17, 2018 (83 FR 46959), in FR Doc.
2018–20090, on page 46960, the
following correction is made:
On page 46960, in the second column,
in section III, in the ‘‘Registration’’ and
‘‘Streaming Webcast of the Public
Workshop’’ portions, ‘‘https://
www.eventbrite.com/e/pathogenreduction-technologies-for-blood-safetypublic-workshop-tickets-4464956605’’ is
corrected to read ‘‘https://
www.eventbrite.com/e/pathogenreduction-technologies-for-blood-safetypublic-workshop-tickets-44649566054.’’
SUPPLEMENTARY INFORMATION:
Dated: October 9, 2018.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2018–22364 Filed 10–12–18; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
BILLING CODE 4120–03–P
[Document Identifier OS–04040–0011]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency Information Collection
Request. 60-Day Public Comment
Request
Food and Drug Administration
AGENCY:
[Docket No. FDA–2018–N–0001]
ACTION:
Pathogen Reduction Technologies for
Blood Safety; Public Workshop;
Correction
SUMMARY:
AGENCY:
Food and Drug Administration,
HHS.
Notice of public workshop;
correction.
ACTION:
The Food and Drug
Administration is correcting a document
that appeared in the Federal Register of
September 17, 2018. The document
announced a public workshop entitled
‘‘Pathogen Reduction Technologies for
Blood Safety; Public Workshop.’’ The
document was published with an error
in the website address to register for the
workshop. This document corrects that
error.
FOR FURTHER INFORMATION CONTACT: Loni
Warren Henderson or Sherri Revell,
Center for Biologics Evaluation and
Research, Food and Drug
Administration, 10903 New Hampshire
Ave., Silver Spring, MD 20993, 240–
SUMMARY:
khammond on DSK30JT082PROD with NOTICES
402–8010, email: CBERPublicEvents@
fda.hhs.gov (subject line: Pathogen
Reduction Technology and Blood
Safety).
VerDate Sep<11>2014
21:34 Oct 12, 2018
Jkt 247001
Office of the Secretary, HHS.
Notice.
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 14,
2018.
Submit your comments to
ed.calimag@hhs.gov or (202) 690–7569.
FOR FURTHER INFORMATION CONTACT:
When submitting comments or
requesting information, please include
the document identifier 4040–0011
New–60D and project title for reference,
to Sherrette.funn@hhs.gov, or call 202–
795–7714, the Reports Clearance
Officer.
ADDRESSES:
Interested
persons are invited to send comments
regarding this burden estimate or any
other aspect of this collection of
information, including any of the
SUPPLEMENTARY INFORMATION:
PO 00000
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51961
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.
Information Collection Request Title:
SF–271 Outlay Report and Request for
Reimbursement for Construction
Programs.
Abstract: The SF–271 Outlay Report
and Request for Reimbursement for
Construction Programs form is by used
grant awardees to request financial
assistance funds for the purpose of
reimbursement of construction-related
expenditures.
Need and Proposed Use of the
Information: The SF–271 Outlay Report
and Request for Reimbursement for
Construction Programs form is used by
grant awardees in post-award financial
activities related to Federal financial
assistance.
Likely Respondents: Federal financial
assistance awardees.
Burden Statement: Burden in this
context means the time expended by
persons to generate, maintain, retain,
disclose or provide the information
requested. This includes 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 the ICs are
summarized in the table below.
HHS estimates that the form will take
1 hour to complete each form.
Once OMB approves the use of the
SF–271 Outlay Report and Request for
Reimbursement for Construction
Programs form as a common form,
federal agencies may request OMB
approval to use this common form
without having to publish notices and
request public comments for 60 and 30
days. Each agency must account for the
burden associated with their use of the
common form.
E:\FR\FM\15OCN1.SGM
15OCN1
]]>Agencies
[Federal Register Volume 83, Number 199 (Monday, October 15, 2018)]
[Notices]
[Page 51961]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-22364]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2018-N-0001]
Pathogen Reduction Technologies for Blood Safety; Public
Workshop; Correction
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice of public workshop; correction.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration is correcting a document that
appeared in the Federal Register of September 17, 2018. The document
announced a public workshop entitled ``Pathogen Reduction Technologies
for Blood Safety; Public Workshop.'' The document was published with an
error in the website address to register for the workshop. This
document corrects that error.
FOR FURTHER INFORMATION CONTACT: Loni Warren Henderson or Sherri
Revell, Center for Biologics Evaluation and Research, Food and Drug
Administration, 10903 New Hampshire Ave., Silver Spring, MD 20993, 240-
402-8010, email: [email protected] (subject line: Pathogen
Reduction Technology and Blood Safety).
SUPPLEMENTARY INFORMATION: In the Federal Register of Monday, September
17, 2018 (83 FR 46959), in FR Doc. 2018-20090, on page 46960, the
following correction is made:
On page 46960, in the second column, in section III, in the
``Registration'' and ``Streaming Webcast of the Public Workshop''
portions, ``https://www.eventbrite.com/e/pathogen-reduction-technologies-for-blood-safety-public-workshop-tickets-4464956605'' is
corrected to read ``https://www.eventbrite.com/e/pathogen-reduction-technologies-for-blood-safety-public-workshop-tickets-44649566054.''
Dated: October 9, 2018.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2018-22364 Filed 10-12-18; 8:45 am]
BILLING CODE 4164-01-P
