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Adverse event
Results: 2359

#	Item
411	PARTNERS HEALTHCARE Research Management Annual Report[removed]About PHS RM Add to Reading List Source URL: navigator.partners.org Language: English - Date: 2014-05-14 14:25:50 Medicine Pharmaceutical industry Design of experiments Pharmacology Nursing research Clinical trial Institutional review board National Institutes of Health Adverse event Clinical research Research Science
412	INSTITUTIONAL REVIEW BOARD IRBNet Assistance CONTENTS GENERAL INSTRUCTIONS AND GUIDANCE……………………………………………………………………………2 Learn about IRBNet Add to Reading List Source URL: uaa.alaska.edu Language: English - Date: 2013-12-02 14:39:44 Science Scientific method Design of experiments Pharmacology Drug safety Institutional review board Portable Document Format Adverse event Grant Clinical research Research Pharmaceutical industry
413	PDF Document Add to Reading List Source URL: icuro.be Language: English - Date: 2013-11-14 04:15:34 Medical terms Healthcare Patient safety organization Health informatics Medical error Electronic health record Adverse event Patient Safety and Quality Improvement Act Never events Medicine Health Patient safety
414	Referencias: 1 Current Pharmaceutical Design 2012 Sep 24. [Epub ahead of print] Add to Reading List Source URL: mercola.fileburst.com Language: English - Date: 2012-11-02 00:31:33 Biology Drug safety Public safety Vaccine Adverse Event Reporting System Gardasil HPV vaccine Human papillomavirus Vaccine Wart Papillomavirus Medicine Vaccines
415	FDA Warning Letter to Center for the Improvement of Human Functioning International, Inc. IRB[removed] Add to Reading List Source URL: www.circare.org Language: English - Date: 2012-08-14 18:04:55 Pharmaceutical sciences Science Design of experiments Food and Drug Administration Drug safety Institutional review board Form FDA 483 Adverse event Clinical investigator Clinical research Pharmacology Research
416	INSTRUCTIONS FOR REPORTING IN-OFFICE SURGERIES OR PROCEDURES INVOLVING CONSCIOUS SEDATION, DEEP SEDATION OR GENERAL ANESTHESIA, AND ANY ASSOCIATED SENTINEL EVENTS, FOR[removed]All allopathic physicians licensed in the Add to Reading List Source URL: www.medboard.nv.gov Language: English - Date: 2015-01-23 13:15:31 Anesthesia awareness Procedural sedation and analgesia General anaesthesia Surgery Sentinel event Patient safety Adverse effect Port Medical error Medicine Anesthesia Sedation
417	INSTRUCTIONS FOR REPORTING IN-OFFICE SURGERIES OR PROCEDURES INVOLVING CONSCIOUS SEDATION, DEEP SEDATION OR GENERAL ANESTHESIA, AND ANY ASSOCIATED SENTINEL EVENTS, FOR[removed]All allopathic physicians licensed in the Add to Reading List Source URL: medboard.nv.gov Language: English - Date: 2015-01-23 13:15:31 Anesthesia awareness Procedural sedation and analgesia General anaesthesia Surgery Sentinel event Patient safety Adverse effect Port Medical error Medicine Anesthesia Sedation
418	CDER Data Standards Strategy Add to Reading List Source URL: www.fda.gov Language: English Medicine Medical informatics Clinical Data Management Clinical trials Clinical Data Interchange Standards Consortium Electronic Common Technical Document Adverse Event Reporting System SDTM Center for Biologics Evaluation and Research Research Food and Drug Administration Clinical research
419	DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration[removed]New Hampshire Avenue Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-12-30 12:09:50 Health Center for Devices and Radiological Health Unique Device Identification Premarket approval Medical device Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Adverse event Investigational Device Exemption Food and Drug Administration Medicine Technology
420	DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration[removed]New Hampshire Avenue Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2015-01-16 15:53:46 Health Medical device Premarket approval Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Unique Device Identification Adverse event Title 21 of the Code of Federal Regulations Investigational Device Exemption Food and Drug Administration Medicine Technology

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