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Unique Device Identification
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411	r:lf:. ~ \-llYI(·(S.(I DEPARTMENT OF HEALTH & HUMAN SERVICES Food and Drug Administration[removed]New Hampshire Ave. Add to Reading List Source URL: www.fda.gov Language: English Technology Food law Unique Device Identification Medical equipment Code of Federal Regulations Medical device Title 21 CFR Part 11 Medicine Food and Drug Administration Health
412	Contents of this document: Add to Reading List Source URL: www.fda.gov Language: English Technology Center for Devices and Radiological Health Medical device Unique Device Identification Medicine Food and Drug Administration Health
413	Contents of this document: Add to Reading List Source URL: www.fda.gov Language: English Health Unique Device Identification Center for Devices and Radiological Health Premarket approval Medical device Adverse event Food and Drug Administration Medicine Technology
414	Microsoft Word - Agenda_Denmark_draft_v16 Add to Reading List Source URL: www.gs1.org Language: English - Date: 2014-07-16 10:43:16 Medicine Universal identifiers Standards organizations Food and Drug Administration Unique Device Identification GS1 Global Data Synchronization Network Traceability Global Trade Item Number Barcodes Identification Identifiers
415	Contents of this document: Add to Reading List Source URL: www.fda.gov Language: English Technology Pharmaceutical industry Unique Device Identification Medical equipment Center for Devices and Radiological Health Pharmaceuticals policy Medical device Premarket approval Adverse event Food and Drug Administration Medicine Health
416	[removed]Federal Register / Vol. 79, No[removed]Friday, June 27, [removed]Notices Dated: June 23, 2014. Leslie Kux, Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2014-06-27 02:20:39 Health Food law Food safety Unique Device Identification Generally recognized as safe Center for Veterinary Medicine Title 21 of the Code of Federal Regulations Animal drugs Food and Drug Administration Food and drink Medicine
417	Customer Recall Notifications Add to Reading List Source URL: www.fda.gov Language: English Technology Class I recall Center for Devices and Radiological Health Medical device Unique Device Identification Office of Regulatory Affairs Food and Drug Administration Medicine Health
418	tkelley on DSK3SPTVN1PROD with NOTICES Federal Register / Vol. 79, No[removed]Friday, July 11, [removed]Notices Supplements Under GDUFA.’’ The Generic Drug User Fee Amendments of[removed]GDUFA) enables FDA to assess Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2014-07-16 16:29:04 Pharmacology Clinical research Pharmaceuticals policy Abbreviated New Drug Application New Drug Application Generic drug ClinicalTrials.gov Unique Device Identification Pharmaceutical industry Food and Drug Administration Pharmaceutical sciences
419	This graph depicts what happens to an adverse event report that is submitted to FDA. First, FDA may receive one of two types of reports: mandatory or voluntary. A mandatory report is sent to FDA by a manufacturer, import Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Clinical research Pharmaceutical industry Therapeutics Adverse event Adverse Event Reporting System Unique Device Identification Pharmaceutical sciences Pharmacology Research
420	EFA briefing January 2013 Roberta Savli Proposal for a regulation of the European Parliament and of the Council on medical devices 1 Add to Reading List Source URL: www.efanet.org Language: English - Date: 2013-08-08 06:44:30 Medical technology Food and Drug Administration Medical device CE mark Medical Devices Directive Unique Device Identification Eucomed GMDN Medicine Technology Medical equipment

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