Overview
*Short Course requires separate registration
Short Course Registration: 1:30-5:00PM
This half-day short course will focus on the analysis of post-market medication error reports and regulatory approaches to prevent medication errors. The course will use a case-based instructional model to cover the principles of medication error pharmacovigilance, case assessment, and the application of regulations and guidances to design labels and labeling to prevent medication errors.
Learning objectives
- Describe the differences and similarities between adverse event and medication error pharmacovigilance
- Apply best practices to code and retrieve medication error reports
- Assess reports to determine the type of medication error and causes or contributing factors
- Adjudicate combination product reports related to device malfunction and usability (use error/device difficult to use)
- Design user interfaces (e.g., labels, labeling) to prevent medication errors
Register for both a morning and afternoon short course and the full conference for $100 off! Registrations must happen at the same time, discounts reflected at checkout.
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Pharamcovigilance and Risk Management Strategies Conference
Other Preconference Short Courses
Short Course 1: Pharmacovigilance and Risk Management Planning
Short Course 2: Interdisciplinary Safety Evaluation During Product Development
Short Course 3: Reference Safety Information
Short Course 4: Introduction to Statistics in Pharmacovigilance