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Adverse event
Results: 2359

#	Item
671	National Action Plan for Adverse Drug Event Prevention Add to Reading List Source URL: www.health.gov Language: Czech - Date: 2014-09-18 06:35:00
672	[removed]IRB Protocol Review Fee Policy Add to Reading List Source URL: www.howard.edu Language: English - Date: 2014-09-17 13:01:04 Science Pharmaceutical industry Medicine Design of experiments Medical ethics Institutional review board Clinical trial Adverse event Grant Clinical research Research Pharmacology
673	Web Summary AE VAERS Updated[removed] Add to Reading List Source URL: vaers.hhs.gov Language: English - Date: 2010-06-03 16:19:38 Health Drug safety Food and Drug Administration Public safety Vaccine Adverse Event Reporting System Influenza vaccine Flu pandemic vaccine FluMist Flu pandemic Medicine Vaccines Vaccination
674	DEPARTMENT OF HEALTH & HUMAN SERVICES April 10, 2014 Public Health Service Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-08-13 16:40:55 Health Medical device Premarket approval Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Adverse event Investigational Device Exemption Unique Device Identification Food and Drug Administration Medicine Technology
675	Guidance for Industry: MedWatch Form FDA 3500A: Mandatory Reporting of Adverse Reactions Related to Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/Ps) Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Center for Biologics Evaluation and Research Adverse effect Adverse Event Reporting System MedWatch Allotransplantation Adverse event Medical device Medicine Food and Drug Administration Health
676	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
677	National Action Plan for Adverse Drug Event Prevention Add to Reading List Source URL: www.health.gov Language: Czech - Date: 2014-09-18 06:35:00
678	Adverse Event Data Preparation Checklist Add to Reading List Source URL: prsinfo.clinicaltrials.gov Language: English - Date: 2014-11-17 12:05:43 Serious adverse event Science Business Knowledge Clinical research Pharmaceutical industry Adverse event
679	BACKGROUNDER Contact: Rend Al-Mondhiry [removed[removed]7672 CRN Debunks Widely Cited AER Statistic for Supplements  Add to Reading List Source URL: www.crnusa.org Language: English - Date: 2012-02-17 14:53:56 Nutrition Pharmacology Food and Drug Administration Ephedra Metabolife Vitamin Adverse event Adverse effect Hydroxycut Medicine Dietary supplements Health
680	National Action Plan for Adverse Drug Event Prevention Add to Reading List Source URL: www.health.gov Language: Czech - Date: 2014-09-18 06:35:00

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