A quick guide to implementing a Clinical MDR

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.

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About Certara

Certara is dedicated to transforming drug discovery and development for good. We harness the power of biosimulation, advanced analytics, and regulatory expertise to create a future where treatments reach patients faster and more efficiently.

From discovery to market access and commercial, we tailor solutions to meet our clients’ most pressing challenges. Through strategic leadership and advanced predictive technologies, Certara provides comprehensive solutions to optimize drug development processes, reduce risks, and improve outcomes. Our clients include more than 2,400 biopharmaceutical companies, academic institutions, and regulatory agencies across 70 countries.