日期： 2025 年 9 月 25 日, 星期四
时间： 12:00 PM EST
Services: Patient Narrative Writing Services
产品： 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.
点击报名
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
Sheppard 女士是全球申报高级总监兼医学作家，在合同研究组织和制药环境领域的文件质量控制、项目管理以及临床透明度和披露方面具有丰富经验。她拥有 20 年的转化科学、临床开发和临床业务经验，其中包括 15 年的医学写作和监管策略经验，涉及生物制剂和小分子的全球上市申请，以及新药临床试验申请 (IND) 和临床试验授权 (CTA) 申请。
点击报名
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!
