Monitoring and Reporting Adverse Drug Reactions
Training Overview
Improve Your Ability to:-
Ensure compliance by accurately reporting drug safety data to FDA
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Implement methods for capturing and processing suspected adverse events
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Effectively manage your MedDRA program in order to help store, retrieve and analyze data
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Comply with current requirements for safety surveillance and reporting and avoid regulatory action
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Analyze the needs and focus of ADR monitoring and reporting programs to increase efficiency and save time
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Use web-based pharmacovigilance to facilitate electronic migration and avoid wasted resources
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Formulate a systematic approach for reporting ADRs to allow appropriate analysis and intervention
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Implement a pharmaceutical risk monitoring system to help protect your patient and your products
PTi international is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmaceutical education. Participants will receive a maximum of 14 hours (1.4 CEUs) of continuing education credit for full participation in the two-day training. ACPE # 326-000-06-017-L04, Initial release: 07/2006.
Booking Options
This course is available exclusively as an onsite training solution. To discuss a solution that fits your organization's needs, objectives, schedule and budget, contact a PTi Client Solutions Manager at 800-303-8194 or OnSiteSolutions@pti-international.com.