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Device register
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#	Item
331	Federal Register / Vol. 69, No[removed]Tuesday, June 1, [removed]Notices project, and their applicability to policy and practice. The provision of a detailed discussion of the objectives and of the extent to which they are Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2010-12-01 23:14:23 Technology Medical device Validation Center for Devices and Radiological Health Center for Biologics Evaluation and Research Title 21 of the Code of Federal Regulations Title 21 CFR Part 11 Unique Device Identification Medicine Food and Drug Administration Health
332	[removed]Federal Register / Vol. 72, No[removed]Wednesday, December 19, [removed]Notices DEPARTMENT OF HEALTH AND HUMAN SERVICES Add to Reading List Source URL: www.fda.gov Language: English - Date: 2007-12-19 08:14:22 Pharmaceutical sciences Federal Food Drug and Cosmetic Act Premarket approval Center for Biologics Evaluation and Research New Drug Application Center for Devices and Radiological Health FDA Warning Letter Unique Device Identification Food and Drug Administration Medicine Health
333	Wednesday, December 15, 2010 Part II Department of Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2013-05-23 11:35:11 Magnuson–Stevens Fishery Conservation and Management Act National Marine Fisheries Service U.S. Regional Fishery Management Councils Rulemaking Turtle excluder device Overfishing Public comment Federal Register Fisheries management Fishing United States administrative law Environment
334	[removed]Federal Register / Vol. 68, No[removed]Wednesday, July 23, [removed]Notices TABLE 1.—ESTIMATED ANNUAL REPORTING BURDEN1 21 CFR Section Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2010-12-01 20:19:45 Pharmaceutical sciences Clinical research Pharmacology Pharmaceutical industry Therapeutics Medical device Validation FDA Center for Devices and Radiological Health Food and Drug Administration Medicine Health
335	[removed]Federal Register / Vol. 68, No[removed]Tuesday, July 8, [removed]Notices Dated: July 1, 2003. Edward Schultz, Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2010-12-01 13:16:42 Pharmaceutical sciences Clinical research Pharmaceutical industry Food law Pharmaceuticals policy Federal Food Drug and Cosmetic Act Medical device Validation Medicine Health Food and Drug Administration
336	[removed]Federal Register / Vol. 72, No[removed]Wednesday, September 12, [removed]Notices DEPARTMENT OF HEALTH AND HUMAN SERVICES Add to Reading List Source URL: www.fda.gov Language: English - Date: 2007-09-12 08:04:56 Pharmaceutical sciences Medical device Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Unique Device Identification Food and Drug Administration Medicine Health
337	. Government Access to Phone Calling Activity and Related Records: Legal Authorities Edward C. Liu Legislative Attorney Add to Reading List Source URL: ipmall.info Language: English - Date: 2012-01-18 19:23:28 Privacy Mass surveillance Privacy law USA PATRIOT Act Pen register Trap and trace device Foreign Intelligence Surveillance Act Section summary of the USA PATRIOT Act Title II National security letter Privacy of telecommunications National security Surveillance
338	[removed]Federal Register / Vol. 72, No[removed]Tuesday, November 6, [removed]Notices DEPARTMENT OF HEALTH AND HUMAN SERVICES Add to Reading List Source URL: www.fda.gov Language: English - Date: 2007-11-06 07:48:20 United States Public Health Service Clinical pharmacology Pharmacology Therapeutics Indian Health Service Thoratec Ventricular assist device United States Department of Health and Human Services Premarket approval Medicine Health Food and Drug Administration
339	[removed]Federal Register / Vol. 69, No[removed]Friday, July 9, [removed]Notices original PMAs, therefore, is 18,275 hours (1,075 approved PMAs with Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2010-12-01 23:13:07 Technology Center for Devices and Radiological Health Medical device Drug Price Competition and Patent Term Restoration Act Federal Food Drug and Cosmetic Act Premarket approval Title 21 of the Code of Federal Regulations New Drug Application Regulatory requirement Food and Drug Administration Medicine Health
340	Federal Register / Vol. 68, No[removed]Monday, September 29, [removed]Notices Director, Division of Respiratory Disease Studies (DRDS), National Institute for Occupational Safety and Health (NIOSH), ALOSH Bldg., Rm. H– 29 Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2010-12-01 20:37:48 Technology Premarket approval Medical device Center for Devices and Radiological Health Validation Food and Drug Administration Modernization Act Federal Food Drug and Cosmetic Act Food and Drug Administration Medicine Health