This educational webinar is 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Clinical trials often face challenges such as inconsistent, unreliable, and outdated metadata.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 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.
本講座で学べる内容
- 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
The course is beneficial for:
- Anyone involved in clinical trials, data management, or data science in Japan
