Resource Library

We’ve compiled a useful collection of resources to learn more about Medrio and various aspects of managing your clinical trial in today’s complex and evolving environment.

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Blog
eConsent

Re-consent in Clinical Trials: Streamlining with eConsent

November 20, 2023
Learn about re-consent challenges, regulatory insights, and the role of eConsent in streamlining informed consent processes.
Blog
RTSM

Is Your Clinical Supply Chain Fully Optimized?

November 15, 2023
Learn unique approaches to study design and supply chain management to better navigate the complex landscape of rare disease clinical trials.
Webinar

Data-based Strategies for Successful Digital Health Technology Clinical Trials

Join industry experts as they discuss the challenges digital health technology organizations face in realizing their solutions' impact.
Blog
CDMS / EDC

How Medrio Protects Your Clinical Trial Data

November 1, 2023
Explore how to keep your clinical trial data safe, secure, and protected in three key steps.
Infographic
CDMS / EDC

Medrio CDMS/EDC Data Security

This infographic highlights how Medrio CDMS/EDC keeps your clinical trial data safe.
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Blog
CDMS / EDCDCTeCOA / ePROeConsentRTSM

Solutions for Hope: Supporting Participants in Rare Disease Trials

October 26, 2023
Navigating the unique complexities of rare disease research is challenging. Discover key strategies and solutions to support participants and reduce overall burden.
Blog
CDMS / EDCDCTeCOA / ePROeConsentRTSM

Empowering Oncology Research with the Right Technology Solutions

October 19, 2023
Uncover solutions for oncology trial success: conquer enrollment and retention obstacles, expedite timelines, and navigate global supply chains.
Blog
CDMS / EDCeCOA / ePROeConsentRTSM

Rare Disease Clinical Trials: Modern Design and Supply Chain

October 10, 2023
Learn unique approaches to study design and supply chain management to better navigate the complex landscape of rare disease clinical trials.
Success Story
CDMS / EDCeCOA / ePROeConsent

Enhancing Large-Scale Data Quality and Compliance: How Medrio Empowers Freenome

Learn how Freenome found a robust partner in Medrio, helping them deliver data quality and compliance for large-scale oncology trials.
eBook

From Bench to Bedside: Evolving Clinical Trial Designs, Protocols and Technology Strategies

Learn about emerging innovations in clinical trial design and execution that support regulatory approval and positive participant experiences.
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Blog

Preparing for the European Medical Device Regulation (EU MDR)

September 29, 2023
Understand how the European MDR (EU MDR) will impact medical device manufacturers and what you can do to prepare.
eBook

European Medical Device Regulation: 5 Steps to Prepare for What’s Coming

Discover how the EU MDR is already impacting companies and learn what you can do to prepare for its full release.
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