Pathogen Reduction Technologies for Blood Safety; Public Workshop; Correction, 51961 [2018-22364]

Download as PDF 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 Frm 00039 Fmt 4703 Sfmt 4703 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]


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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.

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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


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