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Adverse event
Results: 2359

#	Item
931	CDRH PRELIMINARY INTERNAL EVALUATIONS – VOLUME I 510(k) Working Group Preliminary Report and Recommendations August 2010 Add to Reading List Source URL: www.fda.gov Language: English Technology Center for Devices and Radiological Health Premarket approval Medical device Federal Food Drug and Cosmetic Act Adverse event Food and Drug Administration Medicine Health
932	MERP Program & Medication Safety Loriann De Martini, Pharm.D. Chief Pharmaceutical Consultant Center for Healthcare Quality Add to Reading List Source URL: www.cdph.ca.gov Language: English - Date: 2014-08-08 18:30:57 Adverse event Medical error Health Patient safety Medicine Middle-earth Role Playing
933	COMMONWEALTH OF MASSACHUSETTS DEPARTMENT OF MENTAL HEALTH GUIDELINES FOR THE REPORTING OF ADVERSE INCIDENTS RELATING TO RESEARCH The Department Research Review Committee must implement the following guidelines for the re Add to Reading List Source URL: www.mass.gov Language: English - Date: 2014-07-31 12:15:26 Adverse event Serious adverse event Medicine Clinical research coordinator Pharmaceutical industry Clinical research Research
934	FDA-3500A_Instructions_generate pdf_combine with 3-pg vsn.indd Add to Reading List Source URL: www.fda.gov. Language: English Pharmaceutical sciences Pharmacology Pharmaceutical industry Clinical research Patient safety Adverse event Adverse effect Medical device MedWatch Medicine Health Food and Drug Administration
935	Microsoft Word - guidelines_reporting_adverse_events.doc Add to Reading List Source URL: www.mass.gov Language: English - Date: 2014-07-31 12:15:25 Adverse event Serious adverse event Medicine Clinical research coordinator Pharmaceutical industry Clinical research Research
936	MEMORANDUM DEPARTMENT OF HEALTH AND HUMAN SERVICES PUBLIC HEALTH SERVICE FOOD AND DRUG ADMINISTRATION CENTER FOR DRUG EVALUATION AND RESEARCH Add to Reading List Source URL: www.fda.gov Language: English - Date: 2005-06-28 09:23:57 Oxazolidinones Zolmitriptan Pharmaceutical sciences Adverse Event Reporting System Chemistry Clinical research Food and Drug Administration Triptans AstraZeneca Carbamates
937	Microsoft Word - serious_adverse_event_report_form.doc Add to Reading List Source URL: www.mass.gov Language: English - Date: 2014-07-31 12:15:26 Data Technology Adverse event Serious adverse event Email Communications protocol Clinical research Pharmaceutical industry Information
938	FDAs MedWatch Program: Voluntarily Reporting Problems to the FDA Add to Reading List Source URL: www.fda.gov. Language: English MedWatch Health Office of Regulatory Affairs Center for Drug Evaluation and Research Center for Veterinary Medicine Adverse Event Reporting System Adverse effect Food and Drug Administration Pharmaceutical sciences Clinical research
939	Pregnancy Registries: Data collection/experience with vaccines Adel Abou-Ali, PharmD, ScD, MS Deputy Director of Global Pharmacoepidemiology & Risk Management Add to Reading List Source URL: www.fda.gov Language: English Drug safety Food and Drug Administration Public safety Vaccine Adverse Event Reporting System Pregnancy Miscarriage DPT vaccine Medicine Health Vaccines
940	University of Guelph Research Ethics Board (REB) Event Form Definitions: Add to Reading List Source URL: www.uoguelph.ca Language: English - Date: 2014-10-20 14:49:20 Adverse event Incidental findings Knowledge Business Science Clinical research Pharmaceutical industry Serious adverse event

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