Simplify complex patient narrative writing

Producing thousands of patient safety narratives for regulatory submissions can be complex and time-consuming. Join Certara’s RAPS-sponsored webcast to learn how innovative automation and expert strategies simplify patient narrative writing while ensuring compliance, clarity, and consistency.

What you’ll learn in this webinar:

• How automation and intelligent templates streamline patient narrative workflows
• Maintaining quality and compliance with FDA and ICH guidelines
• Combining expert clinical judgment with automation to handle large-scale narrative projects

Why watch this webinar?

Gain actionable strategies to meet tight deadlines, reduce errors, and elevate your regulatory submission quality through effective patient narrative writing workflows.

Who should watch?

Regulatory affairs professionals, pharmacovigilance experts, medical writers, narrative leads, compliance officers, and project managers in pharma and clinical trials will benefit from this webinar.