Learn the best practice approach to implementing a Clinical Metadata Repository
A clinical metadata repository (Clinical MDR or CMDR) can help you effectively store, manage and automate your clinical trial metadata processes. Choosing and implementing a CMDR requires careful planning and execution.
In our short guide, you’ll find a three-step best practice approach to help you choose the right software.
What you’ll learn
Our recommended 3-step approach to choosing and implementing a Clinical MDR, including:
- What to consider when choosing a CMDR, to achieve efficiencies in study build
- How to ensure stakeholders’ needs are met during implementation
- The approach you should take when standardizing metadata, to reduce effort and time spent on study set up
About the author
Erin Erginer, Director of Product
Innovative leader with 20 years of clinical research and healthcare experience, specializing in acquisition, management, and transformation of clinical biospecimen and digital health assessment data. Collaborative creator of tech-enabled solutions for the pharmaceutical industry.
