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Device register
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#	Item
421	[removed]Federal Register / Vol. 77, No[removed]Tuesday, December 4, [removed]Notices and 4 p.m., Monday through Friday, and will be posted to the docket at http:// Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2012-12-04 00:39:37 Pharmaceuticals policy Technology Food law Pharmaceutical industry United States Public Health Service Title 21 of the Code of Federal Regulations Medical device Center for Drug Evaluation and Research Good manufacturing practice Medicine Food and Drug Administration Health
422	Federal Register / Vol. 63, No[removed]Tuesday, November 3, [removed]Rules and Regulations DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration 21 CFR Part 814 [Docket No. 98N–0171] Add to Reading List Source URL: www.fda.gov Language: English Food law Technology Pharmaceuticals policy Pharmacology Clinical research Food and Drug Administration Modernization Act Federal Food Drug and Cosmetic Act Humanitarian Device Exemption Premarket approval Food and Drug Administration Medicine Health
423	Federal Register / Vol. 76, No[removed]Thursday, November 10, [removed]Notices Consumer Assistance, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 66, rm. 4613, Sil Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2013-05-23 11:09:34 Pharmaceutical industry Pharmaceutical sciences Food and Drug Administration Pharmacology Investigational Device Exemption Medical statistics Medical device IDE Clinical trial Research Clinical research Medicine
424	Federal Register / Vol. 78, No[removed]Tuesday, May 28, [removed]Notices mstockstill on DSK4VPTVN1PROD with NOTICES Evaluation and Research (HFM–17), Food and Drug Administration, 1401 Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2013-05-25 00:58:15 Pharmaceutical sciences Food and Drug Administration Pharmaceuticals policy clinical research Equianalgesic Regulatory requirement Center for Biologics Evaluation and Research Unique Device Identification Structured Product Labeling Medicine Health Pharmacology
425	Federal Register / Vol. 79, No[removed]Wednesday, February 19, [removed]Notices DATES). For additional information about the purpose of the meeting, topics for discussion, and registration see the Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2014-02-19 01:00:16 Pharmacology Medicine Food law Pharmaceuticals policy Drug safety Pharmacovigilance Unique Device Identification Structured Product Labeling Pharmaceutical sciences Food and Drug Administration Health
426	Federal Register / Vol. 79, No[removed]Thursday, February 20, [removed]Proposed Rules II. Withdrawal of the Proposed Rule FDA provided an opportunity for interested parties to comment on the proposed rule for SWD for all oth Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2014-04-25 11:04:47 Technology Pharmaceuticals policy Food law Pharmaceutical industry Clinical research Premarket approval Medical device Federal Food Drug and Cosmetic Act Center for Devices and Radiological Health Food and Drug Administration Medicine Health
427	X-ray Registration Fact Sheet Kansas Department of Health and Environment (KDHE) • New X-ray device? Within 30 days, register your device with KDHE Certificate of Registration will be mailed to facility for display Add to Reading List Source URL: www.kdheks.gov - Date: 2012-02-06 17:34:35
428	[removed]Federal Register / Vol. 75, No[removed]Wednesday, August 25, [removed]Proposed Rules List of Subjects in 14 CFR Part 39 Add to Reading List Source URL: www.fda.gov Language: English Technology Food law Pharmaceuticals policy Pharmaceutical industry Clinical research Medical device Investigational Device Exemption Premarket approval Federal Food Drug and Cosmetic Act Food and Drug Administration Medicine Health
429	[removed]Federal Register / Vol. 76, No[removed]Monday, August 29, [removed]Notices Respondents: The respondents will be identified at the time that each change request is submitted to OMB. Generally Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2013-05-23 10:33:16 Clinical research Pharmaceutical industry Food and Drug Administration Pharmacology Nursing research Investigational Device Exemption Investigational New Drug Clinical trial Clinical investigator Medicine Research Health
430	Federal Register / Vol. 77, No[removed]Thursday, August 2, [removed]Rules and Regulations DEPARTMENT OF HEALTH AND HUMAN SERVICES [FR Doc. 2012–18516 Filed 8–1–12; 8:45 am] BILLING CODE 4910–13–P Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2012-08-02 03:38:58 Food law Technology Pharmaceuticals policy Pharmaceutical industry United States administrative law Federal Food Drug and Cosmetic Act Title 21 CFR Part 11 Medical device Premarket approval Food and Drug Administration Medicine Health

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