Clinical Trial Data Services
Change how you compete by getting the clinical data services and support you need. Medrio is here to help clinical trial sponsors and CROs build internal expertise and support any clinical trial data management needs.
Accelerate Study Timelines
Flexible and tailored services to help you move faster.
Improve Clinical Data Integrity
Ensure data quality and cleanliness with an effective data partner.
Enable Internal Teams
From onboarding and implementation to data management, let us fill your resource gaps.
Flexible Data Services Support to Meet Your Needs
Outsourcing your clinical data management will show you the difference an effective data partner makes. You can navigate staff vacancies, onboard new hires, and scale your team with data services that promise quality while ensuring compliance.
Customer Testimonial
Regulatory and Data Processes You Can Trust
Medrio adheres to strict regulatory and industry standards, including ICH, GCP, and regulatory agency guidelines like FDA 21 CFR Part 11. Plus, our standard operating procedures, document templates, and case report form (CRF) templates ensure high-quality output. All processes are CDASH-compliant and rigorously checked.
What Medrio Customers Are Saying
Find out why Medrio has a 98% customer retention rate.
“Built with the builder in mind.”
“One of the easiest systems to implement mid-study updates. Queries are easy to find and respond to. Audit trails are straightforward as well.”
Dan Pontoriero
“The entire team is exceptional.”
“They are reliable and meet timelines. I got the same team members from beginning to end. Working with Ramana was a breath of fresh air!”
Claudia Ramos
SR. DIRECTOR, CLINICAL OPERATIONS
“Data simplified!”
“Medrio provides a system that is versatile and simplifies the complexities of data collection and management for administrators and data managers.”
Anonymous
OUR INTEGRATED SUITE OF SOLUTIONS
Maximize trial efficiency and operational excellence with intuitive clinical data management technology.
Improve data quality, engagement, and retention with a flexible, patient-centric solution.
Efficiently manage informed consent, enhancing compliance and participant experiences.
Drive success by partnering with an effective and strategic project management team.
Proudly Serving Life Science Innovators
Our commitment extends beyond providing solutions; it’s about being a part of a collective effort to drive positive change and innovation in critical sectors of the life science industry.
Frequently Asked Questions
What are Clinical Data Services, and how do they support study teams?
Clinical Data Services provide expert-led support to help sponsors and CROs optimize clinical trial data management. Our team assists with study builds, data strategy, and process optimization, acting as a scalable resource for organizations that need to move quickly without increasing internal headcount.
What are the three phases of Clinical Data Management?
- Data Collection: Gathering participant information via EDC, eCOA, or eConsent.
- Data Processing: Cleaning and validating data to ensure accuracy and protocol compliance.
- Data Analysis: Locking the database and transferring validated data for statistical reporting and regulatory submission.
How do Medrio’s Clinical Data Services specifically benefit pharmaceutical and biopharmaceutical companies?
Medrio helps biopharma companies accelerate speed-to-market by providing data management solutions that align with GxP and CDISC standards. We provide the technical expertise to handle complex Phase I-III protocol designs, ensuring that clinical data infrastructure is inspection-ready for global regulatory submissions.
What is the Functional Service Provider (FSP) model, and how does Medrio implement it?
Our FSP model allows sponsors to outsource specific functions—like data management or clinical reporting—to Medrio experts. This “plug-and-play” expertise scales with your study needs, providing a flexible alternative to full-service outsourcing or permanent internal hiring.
How does Medrio assist with study builds and eCRF design?
Medrio’s Professional Services team specializes in rapid, compliant study builds. We translate complex protocols into optimized eCRFs and databases, ensuring that edit checks and validations are robust from the start to minimize mid-study corrections and accelerate the path to database lock.
Can Medrio help with data migration from legacy systems?
Yes, Medrio provides expert support for migrating data from legacy EDC systems or disparate sources. We manage the mapping and integration process to ensure data integrity is maintained, allowing sponsors to modernize their technology stack without losing historical study insights.
How do these services help ensure regulatory compliance and inspection readiness?
Our services follow validated processes aligned with FDA 21 CFR Part 11, ICH E6(R2) GCP, and GDPR. We provide “audit-ready” workflows, including data governance guidance and audit trail reviews, giving sponsors confidence during regulatory inspections or internal audits.
Do Medrio’s clinical data experts provide training and enablement for internal teams?
Yes. Through our Enablement services, we empower sponsor and CRO teams to become self-sufficient on the Medrio platform. We provide tailored training and best-practice workshops so your internal team can eventually manage studies, design forms, and pull reports independently.
Why should a company choose Medrio over a traditional CRO for clinical data services?
Unlike traditional CROs, Medrio offers deep, specialized expertise specifically within the Medrio unified platform. This results in faster configurations, more efficient troubleshooting, and a technology-first approach that emphasizes agility and a direct partnership with your software provider.
Upholding the Highest Compliance Standards
Ready to see Medrio in action? Let’s get started.
