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Adverse Event Reporting System
Results: 638

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221	CDPH Letterhead (no comma in Jerry Brown Jr) Add to Reading List Source URL: eziz.org Language: English - Date: 2012-10-04 12:39:14 Vaccination Centers for Disease Control and Prevention Vaccines Patient safety Vaccine Adverse Event Reporting System Patient safety organization Vaccine National Childhood Vaccine Injury Act Vaccine injury Medicine Health Drug safety
222	12 Use of Form FDA 3500/3500A for Reporting to FDA Add to Reading List Source URL: www.fda.gov Language: English - Date: 2005-12-06 10:14:57 Pharmaceutical sciences Adverse Event Reporting System MedWatch Center for Biologics Evaluation and Research Center for Devices and Radiological Health New Drug Application Adverse effect Adverse event Medical device Food and Drug Administration Medicine Health
223	What Immunization Providers Need to Know about Vaccine Safety and Talking to Concerned Parents Melinda Wharton, M.D., M.P.H. National Center for Immunization and Respiratory Diseases Add to Reading List Source URL: www.anthc.org Language: English - Date: 2008-11-12 13:34:04 Vaccination Prevention Gardasil HPV vaccine Vaccine Adverse Event Reporting System Vaccine Human papillomavirus Anthrax vaccines Varicella vaccine Vaccines Medicine Papillomavirus
224	DEPARTMENT OF HEALTH AND HUMAN SERVICES Public Health Service Food and Drug Administration College Park, MD Add to Reading List Source URL: www.fda.gov Language: English - Date: 2002-10-30 11:03:09 Clinical research Genetically modified food Dietary supplement Adverse Event Reporting System MedWatch Criticism of the Food and Drug Administration Food and Drug Administration Pharmaceutical sciences Health
225	02N-0445_emc-OOOOOl.txt From: ALLISON CHRISTINEBLILLY.COM Sent: Thursday, January 23, 2003 lo:04 Add to Reading List Source URL: www.fda.gov Language: English - Date: 2004-04-27 17:56:28 Technology New Drug Application Title 21 of the Code of Federal Regulations Medical device Center for Devices and Radiological Health Center for Drug Evaluation and Research Adverse Event Reporting System Center for Biologics Evaluation and Research Design history file Food and Drug Administration Medicine Health
226	BlueCross BlueShield Association +ENii? 4A VV Add to Reading List Source URL: www.fda.gov Language: English* - Date: 2000-11-13 08:53:55 Pharmaceutical sciences Food and Drug Administration Advertising Direct-to-consumer advertising Patient safety MedWatch Piperazines Adverse effect Adverse Event Reporting System Medicine Health Pharmacology
227	Computerized Systems Used in Medical Device Clinical Investigations Presented by Jonathan Helfgott Consumer Safety Officer Division of Bioresearch Monitoring Office of Compliance Add to Reading List Source URL: www.fda.gov. Language: English Food and Drug Administration Technology Pharmaceutical industry pharmacology Adverse Event Reporting System Medical device Clinical investigator Regulatory requirement Electronic patient-reported outcome Clinical research Medicine Research
228	A MEDWATCH CONTINUING EDUCATION ARTICLE Provided as a service by the Staff College, Center for Drug Evaluation and Research, Food and Drug Administration October[removed]THE CLINICAL IMPACT OF ADVERSE EVENT REPORTING Add to Reading List Source URL: www.fda.gov. Language: English Pharmaceutical sciences Pharmacology Clinical research Pharmaceutical industry Drug safety Adverse Event Reporting System MedWatch Adverse effect Postmarketing surveillance Medicine Health Food and Drug Administration
229	GOVERNMENT OF THE DISTRICT OF COLUMBIA DEPARTMENT OF HEALTH HEALTH REGULATION AND LICENSING ADMINISTRATION Patient Safety Reporting System Add to Reading List Source URL: doh.dc.gov Language: English - Date: 2014-07-17 12:48:50 Medical terms Healthcare Patient safety organization Clinical research Pharmaceutical industry Never events Medical error Adverse event ECRI Institute Medicine Health Patient safety
230	ven tis October 8, 2003 Via Fax and UPS Dockets Management Branch (HFA-305) Add to Reading List Source URL: www.fda.gov Language: English - Date: 2003-10-24 18:00:35 Health Adverse Event Reporting System Food and Drug Administration Adverse event Clinical trial Pharmacovigilance Pharmaceutical industry Adverse effect Clinical investigator Pharmacology Pharmaceutical sciences Medicine

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