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Adverse event
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461	FULL TITLE: Protocol No. Add to Reading List Source URL: www.hivnet.ubc.ca Language: English - Date: 2014-12-16 12:40:43 Pharmaceutical industry Scientific method Design of experiments Pharmacology Evaluation methods Clinical trial Case report form Adverse event Institutional review board Clinical research Research Science
462	Doc. No. TFDA/DMC/CTPV/003 TANZANIA FOOD AND RUGS AUTHORITY REPORT ON MONITORING OF ADVERSE DRUG REACTIONS DUE TO ANTIMALARIAL Add to Reading List Source URL: tanzania.go.tz Language: English - Date: 2014-11-12 07:17:07 Medicine Pharmacovigilance Uppsala Monitoring Centre Adverse effect Adverse drug reaction Adverse event Artemether Yellow Card Scheme Postmarketing surveillance Pharmacology Pharmaceutical sciences Health
463	Health Information Technology Adverse Event Reporting: Analysis of Two Databases Add to Reading List Source URL: healthit.gov Language: English - Date: 2014-12-19 08:16:17 Health informatics Healthcare Medical terms Patient safety organization Patient Safety and Quality Improvement Act ECRI Institute Electronic health record Agency for Healthcare Research and Quality Health care in the United States Medicine Health Patient safety
464	Single-site MOOP APPENDICES.docx Add to Reading List Source URL: www.niams.nih.gov Language: English - Date: 2014-11-14 11:54:48 Pharmaceutics Science Serious adverse event Clinical trial Adverse event Methadone X Window System Function Clinical research Pharmaceutical industry Research
465	Multi-site MOOP APPENDICES_1.docx Add to Reading List Source URL: www.niams.nih.gov Language: English - Date: 2014-11-14 14:28:14 Pharmaceutics Science Serious adverse event Clinical trial Adverse event Methadone X Window System Function Clinical research Pharmaceutical industry Research
466	PDUFA V Annual IT Assessment FY2014 Add to Reading List Source URL: www.fda.gov Language: English Health Prescription Drug User Fee Act Investigational New Drug Electronic Common Technical Document New Drug Application Center for Biologics Evaluation and Research Adverse Event Reporting System Common Technical Document Food and Drug Administration Medicine Research
467	National Institute of Arthritis and Musculoskeletal and Skin Diseases Add to Reading List Source URL: www.niams.nih.gov Language: English - Date: 2014-11-14 11:54:20 Science Scientific method Design of experiments Pharmacology Clinical trial Adverse event Institutional review board Case report form Serious adverse event Clinical research Pharmaceutical industry Research
468	National Institute of Arthritis and Musculoskeletal and Skin Diseases Add to Reading List Source URL: www.niams.nih.gov Language: English - Date: 2014-11-14 14:26:51 Science Scientific method Design of experiments Pharmacology Clinical trial Adverse event Institutional review board Case report form Serious adverse event Clinical research Pharmaceutical industry Research
469	Report of the Section 618 Regulations Subgroup - Summary Add to Reading List Source URL: healthit.gov Language: English - Date: 2014-02-28 13:51:01 Pharmaceutical sciences Food and Drug Administration Clinical research Pharmaceuticals policy Medical technology Medical device Patient safety organization Adverse event Good manufacturing practice Medicine Health Pharmaceutical industry
470	Comment by the Federal Institute for Drugs and Medical Devices in coordination with the Paul Ehrlich Institute and the Federal Ministry of Health on Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:27 Pharmaceutical sciences Pharmaceuticals policy Pharmacology Drug safety Clinical Trials Directive Pharmacovigilance Clinical trial Good Clinical Practice Adverse event Clinical research Research Pharmaceutical industry

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