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Unique Device Identification
Results: 463

#	Item
341	Unique Device Identification (UDI) for Medical Devices - Final Report Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Unique Device Identification Barcode
342	FDA’s Home Use Medical Device Initiative Add to Reading List Source URL: www.fda.gov Language: English Health Medical device Center for Devices and Radiological Health Premarket approval Adverse event Unique Device Identification Title 21 CFR Part 11 Food and Drug Administration Medicine Technology
343	CDRH200816[removed]P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration Unique Device Identification System; Proposed Rule Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Pharmacology United States administrative law Unique Device Identification Welfare economics Regulatory Flexibility Act Cost–benefit analysis Inflation Costs Medicine Health Pharmaceutical sciences
344	[removed]Federal Register / Vol. 77, No[removed]Monday, March 12, [removed]Notices ANNUAL BURDEN ESTIMATES Number of respondents Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 05:03:10 Pharmacology Clinical research Clinical pharmacology United States Public Health Service Regulatory requirement Unique Device Identification International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Food and Drug Administration Pharmaceutical sciences Pharmaceuticals policy
345	Links to the Materials from the Subcommittee Meetings Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Clinical pharmacology Therapeutics United States Public Health Service Unique Device Identification Food and Drug Administration Clinical research Pharmaceutical sciences
346	PDF Document Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2012-07-10 01:08:51 Food and Drug Administration Health informatics Medical equipment Unique Device Identification Medical technology Pharmaceutical industry GMDN Medical device Global Harmonization Task Force Medicine Health Technology
347	file://S:TPSACMeetings, Current2011 October Men Add to Reading List Source URL: www.fda.gov Language: English Health policy Menthol cigarette Tobacco Products Scientific Advisory Committee Regulation of tobacco by the U.S. Food and Drug Administration Unique Device Identification Food and Drug Administration Pharmaceutical sciences Clinical research
348	Attachment B CDRH Draft Guidance Cover Sheet Add to Reading List Source URL: www.fda.gov. Language: English Unique Device Identification National Drug Code Data Universal Numbering System Medical device Title 21 CFR Part 11 Structured Product Labeling Validation Health Level 7 Federal Food Drug and Cosmetic Act Medicine Food and Drug Administration Health
349	[removed]Federal Register / Vol. 76, No[removed]Wednesday, April 13, [removed]Notices IV. Electronic Access Persons with access to the Internet Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 12:45:19 Clinical research Food and Drug Administration Regulatory requirement Pharmaceutical industry International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Unique Device Identification Pharmaceutical sciences Pharmacology Pharmaceuticals policy
350	FINAL REPORT OF A STUDY TO EVALUATE THE FEASIBILITY AND EFFECTIVENESS OF A SENTINEL REPORTING SYSTEM FOR ADVERSE EVENT REPORTING OF MEDICAL DEVICE USE IN USER FACILITIES PREPARED UNDER CONTRACT # [removed] Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Pharmacology Adverse event Clinical research Pharmaceutical industry MedWatch Medical device Center for Devices and Radiological Health Unique Device Identification Food and Drug Administration Medicine Health

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