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Date: Thursday, April 3, 2025

Time: 2pm Japan & Korea | 1pm China

Solutions: Regulatory

Summary

Navigating the complexities of clinical data can be challenging, but you’re not alone. In this webinar, we dive into the capabilities of a powerful platform designed to standardize and streamline the entire process from eCRF design to SDTM and other CDISC dataset validation. Discover how this comprehensive solution can enhance efficiency, ensure compliance, and simplify your data management workflows. Whether you’re looking to optimize your current processes or seeking a robust tool to handle complex dataset requirements, this webinar will provide valuable insights and practical strategies to elevate your data management practices.

Join our live webinar as we share insights and strategies to empower you on this journey, helping you transform your clinical data into meaningful insights. Together, we can enhance your understanding and utilization of these essential tools, making a positive impact in your work and beyond.

Register now


What will you learn in the course?

  • How to de-risk and automate submission ready SDTM dataset
  • CDISC and regulatory compliant data validation – validating with the same standard as health authorities

The course will be beneficial for:

  • Anyone who engages in CDISC and SDTM data processing at CROs or pharmaceutical companies/bio ventures

Speakers:

Rico Fujita

Solution Consultant, Certara

Heeyoung Kim

APAC Solution Consultant Manager, Certara

Register now