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Food and Drug Administration / Technology / Pharmaceutical industry / Clinical research / Title 21 CFR Part 11 / United States administrative law / Validation / Paperwork Reduction Act / Medical device / Medicine / Pharmaceuticals policy / Health


[removed]Federal Register / Vol. 79, No[removed]Friday, October 3, [removed]Notices potential sponsors must meet certain conditions pursuant to section 462 of the Homeland Security Act and the
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Document Date: 2014-10-06 08:38:56


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City

Washington / DC / Rockville / /

Company

Clinical Laboratories / /

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Event

Music Album Release / /

Facility

Laboratory Developed Tests / /

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IndustryTerm

electronic media / diagnostic devices / requested emergency processing / in vitro diagnostic devices / information technology / /

MusicAlbum

Information / /

Organization

DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration / Congress / Administration for Children and Families / office of Communication / Outreach / and Development / Center for Devices and Radiological Health / office of Operations / Division of Dockets Management / Availability AGENCY / FDA / Electronic Signatures AGENCY / office of Planning / Research and Evaluation / FDA PRA / office of Management and Budget / office of Information / Center for Biologics Evaluation and Research / Center for Biologics Evaluation and Research Food and Drug Administration / Center for Devices / /

Person

Silver Spring / Peter Lurie / Draft Guidance / Robert Sargis / /

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Position

Clearance Officer / Governor / Director / Commissioner for Policy and Planning / Desk Officer / General / Reports Clearance Officer / /

ProvinceOrState

Maryland / /

Technology

information technology / http / /

URL

www.regulations.gov / /

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