Date: Thursday, September 25, 2025
Time: 12:00 PM EST
Services: Patient Narrative Writing Services
Products: CoAuthor
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 join 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 attend?
Regulatory affairs professionals, pharmacovigilance experts, medical writers, narrative leads, compliance officers, and project managers in pharma and clinical trials will benefit from this webinar.
Register now
Don’t miss this chance to gain actionable insights from Reema SelvaRaju, Associate Director of Patient Safety Narratives & Automation at Certara, and a leader in regulatory writing solutions.
Secure your free spot today!
Associate Director, Patient Safety Narratives & Automation, Certara
Reema SelvaRaju is a microbiologist by training. She has over 15 years of experience in regulatory writing of narratives (pharmacovigilance and clinical study reports; CSR narratives), project management, and using automation technology. SelvaRaju works closely with clients to create custom solutions and ensure smooth project management. She currently leads the narrative space at Certara in the capacity of associate director.
Senior Director, Regulatory Services Management and Lay Language Management Regulatory Science and Medical Affairs
Ms. Sheppard is a senior director of global submissions and medical writer with experience in document quality control, project management, and clinical transparency and disclosure in both contract research organizations and pharmaceutical environments. She has 20 years of experience in translational science, clinical development, and clinical operations, including 15 years in medical writing and regulatory strategy experience with global marketing applications for both biologics and small molecules, as well as for Investigational New Drug (IND) and Clinical Trial Authorization (CTA) applications.
Register now
Don’t miss this chance to gain actionable insights from Reema SelvaRaju, Associate Director of Patient Safety Narratives & Automation at Certara, and a leader in regulatory writing solutions.
Secure your free spot today!
