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Essentials of Safety Medical Writing
Overview
What you will learn
- Introduction of PV documents from beginning of clinical development until the withdrawal of marketing authorization
- DSUR
- BLAs/MAA Clinical Summary of Safety
- RMP
- PBRER/PSUR/PADER
- "Safety concerns" vs "Signals" two concepts at the core of global safety reports
- Overview of relevent data and data sources from clinical trial data to spontaneous reporting
- Safety writing skills: develop key messages: what is the story over time?
Who should attend?
This course is designed for professionals working in:
- Drug safety/pharmacovigilance in R&D, post-market
- Safety risk assessment, benefit-risk assessment
- Risk communication
- Medical writing
- Aggregate reports writing team
- Medical communications
- Clinical/medical
- Clinical informatics, data science, and statistics
- Epidemiology
- Regulatory affairs
- Product labeling
Learning objectives
At the conclusion of this activity, participants should be able to:
- Explain the basic principles of key PV documents
- Identify the relevant data sources and focus on key messages relevant for each report
- Analyze data in a structured way to determine relevant information
- Develop key messages based on data review
- Create reports that meet the needs of your audience