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Adverse event
Results: 2359

#	Item
891	Review of the FDA/CDER Pharmacovigilance Program Add to Reading List Source URL: www.fda.gov Language: English Research Clinical research Food and Drug Administration Pharmaceutical industry Drug safety Pharmacovigilance Adverse event Postmarketing surveillance Clinical trial Pharmacology Pharmaceutical sciences Health
892	Microsoft Word - Executive Summary Add.FINAL-Mail.doc Add to Reading List Source URL: www.fda.gov Language: English Oral surgery Glycosaminoglycans Clinical research Pharmaceutical industry Restylane Lip enhancement Hyaluronan Clinical trial Adverse event Medicine Surgery Oral and maxillofacial surgery
893	GHTF SG2 -National Competent Authority Report Exchange Criteria and Report Form - September 2005 Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-13 17:52:52 Technology Global Harmonization Task Force Medical device National Center for Atmospheric Research GMDN Food and Drug Administration Adverse event Medicine Medical equipment Health
894	24 Sept 11 Event Memo HAI Europe Open Seminar Add to Reading List Source URL: haieurope.org Language: English - Date: 2012-02-02 08:13:34 Pharmacology Pharmacy Pharmaceutical industry Clinical research Drug safety European Medicines Agency PharmedOut Regulation of therapeutic goods Adverse effect Pharmaceutical sciences Health Medicine
895	EXHIBIT 285 WORKSHEET OBQM & OBQI REPORTS - PRE-SURVEY PROCESS AND SAMPLE SELECTION Adverse Event Outcome Report (for most recent quarter, or longer if necessary to reach 60 patients) Tier 1 AE Outcomes Add to Reading List Source URL: www.cms.gov Language: English - Date: 2013-11-22 11:26:30
896	Medical Officer’s Review of Safety Update Report NDA #: 22-222 Add to Reading List Source URL: www.fda.gov Language: English Pancrelipase Exocrine pancreatic insufficiency Chronic pancreatitis Cystic fibrosis Steatorrhea Adverse event Fibrosing colonopathy Malabsorption Shwachman–Bodian–Diamond syndrome Pancreas disorders Health Medicine
897	Version date: 2010 Appendix J Adverse Event Reporting Template Notes to Researcher: Adverse Effects/Unexpected Events Add to Reading List Source URL: www.hc-sc.gc.ca Language: English - Date: 2014-05-12 14:16:52 Health Pharmaceutical industry Pharmacology Medical ethics Patient safety Adverse event Informed consent Risk Adverse effect Clinical research Medicine Research
898	GHTF SG2 Meeting Minutes - April 1999 Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-13 17:52:42 Global Harmonization Task Force Health Medical device Adverse event Food and Drug Administration Guidance document Medicine Medical equipment Technology
899	FDAAA Accomplishments – One Year After Enactment Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Prescription Drug User Fee Act Adverse Event Reporting System ClinicalTrials.gov Center for Biologics Evaluation and Research Federal Food Drug and Cosmetic Act Unique Device Identification Validation Direct-to-consumer advertising Food and Drug Administration Medicine Health
900	FDA POST-MARKET DRUG SURVEILLANCE: IN NEED OF AN OVERHAUL by Katie Zingg FOOD & DRUG LAW Add to Reading List Source URL: www.iflr.msu.edu Language: English - Date: 2011-03-29 12:13:02 Health Drug safety Clinical research Pharmaceutical industry Adverse Event Reporting System Pharmacovigilance Center for Drug Evaluation and Research Approved drug MedWatch Food and Drug Administration Pharmaceutical sciences Pharmacology

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