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Center for Devices and Radiological Health
Results: 3105

#	Item
431	INSTRUCTOR’S GUIDE REGULATORY PATHWAYS FOR PEDIATRIC MEDICAL DEVICES: MARKETING A PEDIATRIC MEDICAL DEVICE VIA A HUMANITARIAN DEVICE EXEMPTION INTRODUCTION Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical industry Clinical research Technology Medical device Premarket approval Center for Devices and Radiological Health Adverse event Investigational Device Exemption Validation Medicine Food and Drug Administration Health
432	Microsoft Word - Agenda PAC meeting Final.docx Add to Reading List Source URL: www.fda.gov Language: English Security National security Food and Drug Administration Center for Devices and Radiological Health Biometrics
433	[removed]UNITED STATES OF AMERICA DEPARTMENT OF HEALTH AND HUMAN SERVICES FOOD AND DRUG ADMINISTRATION +++ Add to Reading List Source URL: www.fda.gov Language: English Technology Medical device Center for Devices and Radiological Health Premarket approval Medicine Food and Drug Administration Health
434	DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration Center for Devices and Radiological Health Add to Reading List Source URL: www.fda.gov Language: English Prostate cancer Premarket approval Prostate Anatomy Medicine Food and Drug Administration
435	FDA Patient Safety News: Show #104, November 2010 Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Pharmaceutical industry Clinical research United States Public Health Service Adverse event MedWatch Package insert Office of Criminal Investigations Center for Devices and Radiological Health Food and Drug Administration Medicine Pharmaceutical sciences
436	Navigating the Pathway From Product Development to Introduction Martha Brady, M.S. Senior Associate, Population Council Presentation at the MDAWG 2012 Meeting Add to Reading List Source URL: www.rhsupplies.org Language: English - Date: 2014-04-17 10:34:00 Pharmacology Health Pharmaceuticals policy Pharmaceutical industry Regulatory requirement European Medicines Agency Biologic Center for Biologics Evaluation and Research Center for Devices and Radiological Health Pharmaceutical sciences Clinical research Food and Drug Administration
437	DEPARTMENT OF HEALTH&. HUMAN SERVICES JUL [removed]Public Health Service Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-06-11 12:35:31 Technology Premarket approval Center for Devices and Radiological Health Medical device Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Investigational Device Exemption New Drug Application Medicine Food and Drug Administration Health
438	Joint Meeting of the Dental Products Panel of the Medical Devices Advisory Committee of the Center for Devices and Radiological Health and the Peripheral and Central Nervous System Drugs Advisory Committee of the Center Add to Reading List Source URL: www.fda.gov Language: English - Date: 2006-09-18 15:32:59 Technology Premarket approval Center for Devices and Radiological Health Medical device Federal Food Drug and Cosmetic Act Investigational Device Exemption Food and Drug Administration Medicine Health
439	1 UNITED STATES OF AMERICA DEPARTMENT OF HEALTH AND HUMAN SERVICES FOOD AND DRUG ADMINISTRATION +++ CENTER FOR DEVICES AND RADIOLOGICAL HEALTH Add to Reading List Source URL: www.fda.gov Language: English Doctor of Medicine Higher education David Sarwer Baylor College of Medicine Education Academia Knowledge
440	DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration Rockville MD 20857 Add to Reading List Source URL: www.fda.gov Language: English - Date: 2007-10-10 08:55:50 Vascular surgery Federal Food Drug and Cosmetic Act Medical device Premarket approval Carotid stenting Medicine Food and Drug Administration Center for Devices and Radiological Health

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