Summary
This educational webinar series will be available only in Japanese.
Clinical trials often face challenges such as inconsistent, unreliable, and outdated metadata. These issues can lead to delays and increased costs. A Clinical Metadata Repository (CMDR) serves as a centralized, reliable library of metadata assets, including forms, terminologies, and datasets, ready for use and reuse.
In this webinar, we will dive into the critical role of standardization, particularly through the use of the Clinical Metadata Repository (CMDR). Whether you’re considering implementing a CMDR or looking to optimize your current processes, this session will provide valuable insights on accelerating drug development by enhancing clinical data management, streamlining metadata use, and improving data quality.
What will you learn in the course?
- Taking silo metadata and standardizing for future use and re-use
- Standard governance and visibility of metadata for maximum efficiency
- Being up-to-date with the latest CDISC Standards
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Solution Consultant, Software, APAC (Japan)
Rico Fujita is a Software Solution Consultant in Japan, APAC. As a Software Solution Consultant, she specializes in understanding customers’ unmet needs and providing technical solutions through in-depth product knowledge, tailored demonstrations, and strategic insights. Prior to joining Certara, Rico worked at Fortrea (formerly known as Labcorp/Covance) as a Clinical Research Associate, and she has hands-on experience in clinical operations with a deep understanding of the challenges faced when delivering treatments to patients.
Her primary focus is to identify and deliver the most effective solutions tailored to each clients’ critical business issues, ultimately bringing efficient and innovative workflow. With a customer-centric mindset, she is dedicated to helping customers achieve their short and long-term goals for their drug development while enhancing their overall experience of Certara’s software solutions.
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