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Regulatory Information
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2016-12-03
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Agency Information Collection Activities; Proposed Collection; Comment Request; Recommended Glossary and Educational Outreach To Support Use of Symbols on Labels and in Labeling of In Vitro Diagnostic Devices Intended for Professional Use
Notices
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D09002ee1bdc0323d
United States
Department of Health and Human Services
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org
United States Government Agency or Subagency
United States
Food and Drug Administration
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org
United States Government Agency or Subagency
The Food and Drug Administration (FDA) is announcing an opportunity for public comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of 1995 (the PRA), Federal Agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on recommended glossary and educational outreach to support use of symbols on labels and in labeling of in vitro diagnostic devices intended for professional use.
81 FR 87570
https://www.govinfo.gov/app/details/FR-2016-12-05/2016-29104
2016-29104
fr05de16-68
4164-01-P
Docket No. FDA-2013-N-1089
https://www.govinfo.gov/app/details/FR-2016-12-05/2016-29104
https://www.govinfo.gov/content/pkg/FR-2016-12-05/html/2016-29104.htm
https://www.govinfo.gov/content/pkg/FR-2016-12-05/pdf/2016-29104.pdf
3 p.
87570
87572
81 FR 87570
Agency Information Collection Activities; Proposed Collection; Comment Request; Recommended Glossary and Educational Outreach To Support Use of Symbols on Labels and in Labeling of In Vitro Diagnostic Devices Intended for Professional Use; Federal Register Vol. 81, Issue
NOTICE
2016-29104
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
2017-02-03
Docket No. FDA-2013-N-1089
4164-01-P
2016-29104
Notice.
The Food and Drug Administration (FDA) is announcing an opportunity for public comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of 1995 (the PRA), Federal Agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on recommended glossary and educational outreach to support use of symbols on labels and in labeling of in vitro diagnostic devices intended for professional use.
Submit either electronic or written comments on the collection of information by February 3, 2017.
FDA PRA Staff, Office of Operations, Food and Drug Administration, Three White Flint North 10A63, 11601 Landsdown St., North Bethesda, MD 20852, PRAStaff@fda.hhs.gov.
Agency Information Collection Activities; Proposals, Submissions, and Approvals:
Recommended Glossary and Educational Outreach to Support Use of Symbols on Labels and in Labeling of In Vitro Diagnostic Devices Intended for Professional Use
,
PRAStaff@fda.hhs.gov
http://www.fda.gov/regulatoryinformation/dockets/default.htm
https://www.regulations.gov
Federal Register
Vol. 81, no. 233
Office of the Federal Register, National Archives and Records Administration
2016-12-05
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399 p.
Table of Contents:
AE 2.7:
GS 4.107:
AE 2.106:
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https://www.govinfo.gov/app/details/FR-2016-12-05
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https://www.govinfo.gov/app/details/FR-2016-12-05
https://www.govinfo.gov/content/pkg/FR-2016-12-05/pdf/FR-2016-12-05.pdf
https://www.govinfo.gov/content/pkg/FR-2016-12-05/xml/FR-2016-12-05.xml
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