How to Evaluate AI Tools for Clinical Trials
August 5, 2026
Learn how to safely evaluate AI tools for clinical trials to manage compliance and reduce risk.
Blog
What Medrio’s 2026 Roadmap Means for You
July 13, 2026
Learn what solution updates are on the horizon, including CTMS, eTMF, and more.
The Evolution of Clinical Data Management Careers
July 6, 2026
See the research showing how CDM roles are changing. Plus, peer advice and actions for how to stay ahead.
What is eTMF in Clinical Trials?
June 22, 2026
Discover how an electronic trial master file (eTMF) creates an inspection-ready source of truth. Learn about its benefits, main users, and EDC integrations.
Why Users Ranked Medrio EDC #1 on G2
May 28, 2026
In the Summer 2026 EDC report, Medrio received high satisfaction ratings across several categories.
How to Improve Your EDC Study Build
April 22, 2026
Learn what to look for in an EDC to support quick, quality study builds.
CTMS: What It Is and How It Supports Clinical Trials
April 17, 2026
Learn what a clinical trial management system (CTMS) does and how it can benefit your trials.
Choosing the Right EDC for Your Rescue Study
March 27, 2026
Learn what to look for in an EDC for a rescue study and why Medrio was built to handle exactly these kinds of high-pressure situations.
Medrio Launches CRO Partner Program
March 13, 2026
Learn more about Medrio’s CRO Partner program.
What to Look For in an EDC for Clinical Trials
February 5, 2026
Learn what your peers are focusing on when purchasing an EDC for clinical trials.
What You Should Know About Medrio Clinical Data Services
January 14, 2026
Learn about the comprehensive clinical trial data services offered by Medrio.
Twenty Years of Teamwork: Top Medrio Moments
September 22, 2025
Meridians look back on 20 years of teamwork, innovation, and supporting research through eClinical technology.
ICH E6(R3) Explained: Insights for European Clinical Trials
August 5, 2025
Understand how ICH E6(R3) is defined, timelines, and ways to prepare.
How to Navigate FDA De Novo Clinical Trials
July 30, 2025
Read this blog to understand the De Novo pathway for medical devices, including best practices, design tips, and more.
Digital Behavioral Therapy for Fibromyalgia
July 23, 2025
Learn about the process of running digital therapeutic trials to receive FDA De Novo marketing authorization.
IRT in Clinical Trials: A Practical Guide for Supply Chain and Clinical Ops
July 16, 2025
Read this blog to learn IRT definitions, benefits, primary functions, and more.
Natural Killer Cells Show Promise in Alzheimer’s Trials
July 7, 2025
Hear from Dr. Paul Song about leading innovative clinical trials, overcoming skepticism, and believing in good science.
Pioneering Treatments for Rare Pediatric Diseases
June 25, 2025
Hear from Dr. Gurdyal Kalsi about the unique aspects of leading research for rare pediatric diseases.
Stability Within Clinical Trials Amidst Uncertainty
May 27, 2025
Watch this interview to learn how Medrio is providing a stable base for clinical researchers amidst uncertainty and why standardization is key to success.
CDMS Software: What to Know for Your Clinical Trials
May 5, 2025
In this blog, learn how Medrio’s CDMS can help you run efficient, compliant, and impactful clinical trials.
Clinical Trials Medical Device Guidelines: What Sponsors Should Know
March 26, 2025
Curious about medical device clinical trials? Learn tips on regulations, trial design, technology, and more!
Database Lock in Clinical Trials: How to Make the Process Easier and Faster
March 3, 2025
In this blog, learn field-tested tips on how to get to database lock (DBL) in clinical trials as quickly as possible.
How the EU AI Act Affects Clinical Trials
February 24, 2025
In this blog, explore how the EU AI Act impacts clinical trials, from risk classification to compliance strategies.
What Is eSource in Clinical Trials?
February 3, 2025
In this blog, discover what eSource is, how it works, and why it benefits clinical trials.
How AI in Clinical Trials Shapes the Future
January 13, 2025
In this blog, discover how AI is rippling through every segment of clinical trials and how to navigate the new landscape.
Artificial Intelligence in Clinical Trials: The Current State of Global Regulatory Frameworks
November 6, 2024
In this blog, understand the current state of published regulatory frameworks for AI in clinical trials.
Preparing for the CTIS: How the EU CTR Impacts Clinical Trials
October 8, 2024
In this blog, learn actionable tips to prepare for the Clinical Trials Information System (CTIS) under the EU CTR.
EDC in Clinical Trials: What It Is & Tips for Success
September 18, 2024
The right EDC system can set researchers up for success in building faster, more robust trials. Read more to learn the essential EDC building blocks.
Clinical Trial Technology Trends for BioPharma and CROs
September 12, 2024
Discover which eClinical tools small biopharma and CROs value most. Explore the latest clinical trial technology trends.
RTSM in Clinical Trials: A Guide to Randomization and Trial Supply Management
September 5, 2024
Discover the role RTSM plays in effective clinical trials and how to choose the right solution for success in our simple guide.
Securing Biopharma & Biotech Funding in a Risk-Averse Market
August 13, 2024
After a 2021 peak, biotech IPOs slump while private funding rises. Find out how to attract clinical research investments today.
How to Optimize Query Management in Clinical Trials
August 8, 2024
Boost data quality in clinical trials with robust query management. Discover strategies now!
What to Know: FDA Laboratory Developed Tests (LDT) Final Rule
July 8, 2024
Learn everything you need to know about the FDA Laboratory Developed Tests (LDT) final rule!
ePRO vs Paper: Patient-Reported Outcome Strategies in Clinical Trials
June 26, 2024
Gain insights on boosting efficiency, accuracy, and compliance with ePRO.
What Are Decentralized Clinical Trials?
May 24, 2024
Discover how DCTs work, why they matter, and how they’re changing trial research in this easy guide.
The State of Gene Therapy Clinical Research
May 8, 2024
Learn about the intersection of technology and science expediting gene therapy clinical research.
How Health Information Technology is Transforming Human Lives
May 1, 2024
From AI to gene therapy, learning how healthcare technology is redefining the future of humanity.
How Standardizing Data Collection Enables Scalability in Clinical Trials
April 25, 2024
Learn from Roche Diagnostics about how to standardize electronic data capture for higher quality data and scalability.
2024 MedTech Regulatory Updates: 4 Areas of Interest
March 21, 2024
Learn key areas of focus for MedTech regulations in 2024, as trials become more complex and new technologies continue to emerge.
Rare Disease Research: Finding Participants and Driving Progress
February 26, 2024
Explore recruitment and engagement strategies in the dynamic landscape of rare disease research, where participants and advocates drive progress.
Supporting Early Phase Oncology Research with the Right Data Management System
February 20, 2024
Innovating in early phase oncology trials requires the right clinical data management system. Find out what to look for!
ePROM Implementation: 4 Best Practices for System Functionality
February 13, 2024
Understand best practices for implementing electronic patient-reported outcome measures (ePROM).
Overcoming Real-World Data Capture Challenges in Phase IV Trials
January 22, 2024
Learn how to leverage real world data (RWD) and real world evidence (RWE) for impactful phase IV clinical trials.
Mastering eConsent: 3 Proven Implementation and Adoption Best Practices
January 5, 2024
Unlock the benefits of electronic consent (eConsent) with our expert insights on adoption and implementation.
Strategies to Unlock Excellence in Digital Health Technology Clinical Trials
December 19, 2023
Discover expert insights for digital health technology clinical trials, including regulatory strategies, endpoint selection, and trial design tips.
Clinical Research 2023: Highlights and Headlines
December 15, 2023
Dive into the highs and lows of 2023 in clinical research! Explore groundbreaking studies, regulatory milestones, and the latest in digital therapeutics in this year’s top news recap.
Generating Quality Data to Streamline Trials and Support Approvals
December 1, 2023
Uncover clinical trial design and execution solutions for collecting high-quality data for approvals.
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.
Is Your Clinical Supply Chain Fully Optimized?
November 15, 2023
Unlock key clinical trial supply chain optimization strategies to ensure efficient logistics, reduce waste, and streamline operations.
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.
How to Support 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.
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.
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.
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.
How Data Is Reshaping the Future of Clinical Trials
September 1, 2023
Data management in clinical research is at an inflection point. Learn what you can do to create more accurate, high-quality clinical trials.
The Moral Obligation: Digital Data Capture for Patient-Centric Trials
August 4, 2023
Digital data capture, such as electronic data capture (EDC), ePRO, and eConsent, create patient centricity and enable accurate data collection.
Why eSource Ensures Data Integrity in Medical Device Clinical Trials
July 14, 2023
Understand the challenges with source data verification and learn how eSource affects clinical trials and improves data integrity.
Importance of Quality Data in Meeting Increasing FDA Regulatory Scrutiny
May 17, 2023
Partnering with a reliable EDC vendor to ensure your clinical trial data meets high standards of accuracy and integrity is essential for passing FDA scrutiny. Risk-based approaches and improved monitoring workflows can help researchers stay ahead of the curve in navigating any potential challenges posed by the FDA, reducing the risk of warnings, rejections or costly additional research.
Want to Boost Retention and Drive Trial Success? You Need Participant Comprehension, Not Consent
May 16, 2023
eConsent is transforming the informed consent process, making it easier for would-be trial participants to understand what’s required of them and providing sponsors with real data on participant comprehension. It’s an important step towards a future of secure, efficient clinical research that serves everyone involved.
Practical Database Design Tips to Maximizing Data Efficiency
May 10, 2023
Effective database design is essential for successful clinical studies, as it improves data quality and accuracy and increases the speed of trial times. This can be done by ensuring the database is user-friendly, utilizing new technologies such as eSource, regularly checking data trends, focusing on SDTM while designing the database, and consulting with sites to proactively address any irregularities. Ultimately, accelerated trial times rely heavily on effective database design.