
ICH E6(R3) Explained: Insights for European Clinical Trials
Understand how ICH E6(R3) is defined, timelines, and ways to prepare.
Understand how ICH E6(R3) is defined, timelines, and ways to prepare.
Read this blog to understand the De Novo pathway for medical devices, including best practices, design tips, and more.
Learn about the process of running digital therapeutic trials to receive FDA De Novo marketing authorization.
Read this blog to learn IRT definitions, benefits, primary functions, and more.
Hear from Dr. Paul Song about leading innovative clinical trials, overcoming skepticism, and believing in good science.
Hear from Dr. Gurdyal Kalsi about the unique aspects of leading research for rare pediatric diseases.
Watch this interview to learn how Medrio is providing a stable base for clinical researchers amidst uncertainty and why standardization is key to success.
In this blog, learn how Medrio’s AI-enabled reporting will help you better understand your clinical trial data.
In this blog, learn how Medrio’s AI-enabled reporting will help you better understand your clinical trial data.
Curious about medical device clinical trials? Learn tips on regulations, trial design, technology, and more!
In this blog, learn field-tested tips on how to get to database lock (DBL) in clinical trials as quickly as possible.
In this blog, explore how the EU AI Act impacts clinical trials, from risk classification to compliance strategies.
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