Books on the topic 'Adverse events reporting'
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Osman, Mansoor, ed. Immunization safety surveillance: Guidelines for managers of immunization programmes on reporting and investigating adverse events following immunization. World Health Organization, Regional Office for the Western Pacific, 1999.
Find full textHealth, Zambia Ministry of. Guidelines for detecting and reporting adverse drug or vaccine reactions and events in Zambia: The safety of medicines in Zambia : why health workers need to take action. National Pharmacovigilance Unit, 2006.
Find full textSaskatchewan. Joint Committee on Drug Utilization. Drug Adverse Event Reporting in Saskatchewan. s.n, 1986.
Find full textHealth, Zambia Ministry of, and Pharmaceutical Regulatory Authority (Zambia). National Pharmacovigilance Unit., eds. Guidelines for detecting and reporting adverse drug or vaccine reactions and events in Zambia: The safety of medicines in Zambia : why health workers need to take action. National Pharmacovigilance Unit, 2006.
Find full textHealth, Zambia Ministry of, and Pharmaceutical Regulatory Authority (Zambia). National Pharmacovigilance Unit., eds. Guidelines for detecting and reporting adverse drug or vaccine reactions and events in Zambia: The safety of medicines in Zambia : why health workers need to take action. National Pharmacovigilance Unit, 2006.
Find full textMegan, Beckett, ed. A review of current state-level adverse medical event reporting practices: Toward national standards. RAND Corporation, 2006.
Find full text1946-, Drazen Jeffrey M., Institute of Medicine (U.S.). Forum on Drug Discovery, Development, and Translation., and Institute of Medicine (U.S.). Board on Health Sciences Policy., eds. Adverse drug event reporting: The roles of consumers and health-care professionals : workshop summary. National Academies Press, 2007.
Find full textBrown, Michael A. A history of a cGMP medical event investigation. John Wiley & Sons, 2013.
Find full textRay, Sumantra (Shumone), Sue Fitzpatrick, Rajna Golubic, Susan Fisher, and Sarah Gibbings, eds. Safety reporting. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199608478.003.0019.
Full textAlbrecht, Douglas. Guide to Reporting and Data Mangement of Adverse Events Involving Medical Devices. Wiley & Sons, Incorporated, John, 2011.
Find full textGuffey, Patrick J., and Martin Culwick. Adverse Event Prevention and Management. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199366149.003.0009.
Full textWHO Regional Office for the Western Pacific. Immunization Safety Surveillance: Guidelines for Immunization Programme Managers on Surveillance of Adverse Events Following Immunization. World Health Organization, 2015.
Find full textWHO Regional Office for the Western Pacific. Immunization Safety Surveillance: Guidelines for Immunization Programme Managers on Surveillance of Adverse Events Following Immunization. World Health Organization, 2014.
Find full textDetection and prevention of adverse drug events: Information technologies and human factors. IOS Press, 2009.
Find full textIroaga, Uchenwa. The incidence and characterization of adverse drug events in the critical care unit: development and implementation of a reporting methodology. 2000.
Find full textAdverse Drug Event Reporting. National Academies Press, 2007. http://dx.doi.org/10.17226/11897.
Full textDutton, Richard P. Creating a Quality Management Program. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199366149.003.0014.
Full textAdverse Event Reporting for Dietary Supplements: An Inadequate Safety Valve. Diane Pub Co, 2001.
Find full textScrip's Essential EEC Texts: Medical Device, Medical Device Vigilance and Adverse Event Reporting. Brookwood Medical Publications Ltd, 1999.
Find full textBegg, Heather. Adverse Drug Event Reporting : The Roles of Consumers and Health-Care Professionals: Workshop Summary. National Academies Press, 2007.
Find full textBegg, Heather. Adverse Drug Event Reporting : The Roles of Consumers and Health-Care Professionals: Workshop Summary. National Academies Press, 2007.
Find full textBegg, Heather. Adverse Drug Event Reporting : The Roles of Consumers and Health-Care Professionals: Workshop Summary. National Academies Press, 2007.
Find full textDevelopment, and Translation Forum on Drug Discovery (Editor), Jeffrey M. Drazen (Editor), Jennifer Rainey (Editor), Heather Begg (Editor), and Adrienne Stith Butler (Editor), eds. Adverse Drug Event Reporting: The Roles of Consumers and Health-Care Professionals: Workshop Summary. National Academies Press, 2007.
Find full textPainter, Lisa M., Cheryl Janov, and Richard L. Simmons. Patient Safety and Quality Improvement (DRAFT). Edited by Raghavan Murugan and Joseph M. Darby. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190612474.003.0034.
Full textA Review of Current State-Level Adverse Medical Event Reporting Practices: Toward National Standards (Technical Report). RAND Corporation, 2006.
Find full textStoelting, Robert K. Patient Safety. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199366149.003.0001.
Full textMcDougald, Laura. Recommendations for the implementation of an adverse drug event reporting and monitoring system for Hamilton Health Sciences Corporation. 1998.
Find full textSharon, Robert, and Erik Eberhardt, eds. Guidelines for Slope Performance Monitoring. CSIRO Publishing, 2020. http://dx.doi.org/10.1071/9781486311002.
Full textStaender, Sven, and Andrew Smith. Safety and quality assurance in anaesthesia. Edited by Philip M. Hopkins. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199642045.003.0036.
Full textGrant, Robert. Tumours of the brain and skull. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780198569381.003.0624.
Full textReading, Paul. Sleep disorders. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780198569381.003.0736.
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