Proven, powerful and scalable clinical trial EDC solutions from do-it-yourself to do-it-all

It can be daunting to collect and manage data — whether for single studies, complex development portfolios or entire development programs. At Clario, we’ve been facing and overcoming EDC challenges for more than 20 years. We’ve learned a few things along the way. And we’re excited to share them with you.

One insight we’ve gained is that some of our clients wish to build a clinical trial EDC solution themselves. Without big up-front costs or long-term commitments. Others seek a more full-featured solution with a higher level of service and no day-to-day hassles.

Clario’s EDC suite of solutions — delivered through a single, powerful, flexible platform — enables you to:

  • Eliminate obstacles
  • Operate more efficiently
  • Manage data for one study or a global portfolio of clinical trials

You can trust Clario to help you find the right approach and scale it appropriately. We have deployed trials in over 120 countries and operate from 30 facilities in 8 countries.

You also can trust the security of our system. Our recent CyberVadis score of 925 demonstrates our commitment to data privacy and GDPR, data protection, third-party management and business continuity.

Our trial oversight solutions — including EDC — provide analytics and insights that identify issues and help maintain the reliability of your data.

Another observation we’ve made is that some organizations desire a full-service partner — someone to build and manage their clinical trial EDC solution and maybe even add on fully integrated data management services.

Here’s the complete range of Clario’s EDC solutions you can choose from to meet your needs:

EDC Solo: The power of simplicity.

Clario EDC License + Study Builder + Library Services

EDC Control: Strength in numbers. Ease in implementation.

Clario EDC License + Project Management + Build Services

EDC Command: Harness the power. Eliminate the obstacles.

Clario EDC License + Project Management + Build Services + Data Management & Statistics

Learn how Trennic Data Services LLC uses EDC Solo to build studies for their clients

With Clario EDC for clinical trials you get more, so you can do more

You can see deeper into each study. Streamline processes across an entire development pipeline. And not just capture data, but effectively manage it and make the most of it. Because everything you need is built in.

This is why Clario is the partner of choice for many leading research programs worldwide.

  • eSource made simple with easy-to-use tools for quick and efficient data collection right at the source
  • Integrated Clario IRT for randomization, dosing and kit assignments that won’t compromising power or performance
  • Value for all stakeholders with tools tailored for data managers, site investigators, monitors and member of operations groups

Watch our Clario EDC Solo demo video

Our three EDC options in detail

The power of simplicity.

Why go Solo?

Your task is to collect and manage the data for one or more studies. But you don’t want to spend a lot of money on it — or make a big, up-front commitment.

So, you turn to the easy, affordable solution with enough flexibility and firepower to take care of the trials in front of you and support your long-term success.

Solo: a simple, powerful tool.

  • Proven real-world functionality
  • Based on Clario’s extensive EDC know-how
  • Scalable — so it can support single or multiple studies and trials of any size
  • Supported by our experienced data management and study build teams

Strength in numbers. Ease in implementation.

Why take control?

You’re running multiple studies and need easy access to your data. But you don’t need the overhead and maintenance hassles of building it yourself — and you don’t want to waste your time or money.

So, you take advantage of the powerful, efficient, integrated system that puts everything you need at your fingertips.

When you’re in Control, we build it, you manage it.

  • Full-service support from EDC experts with 20+ years of experience
  • An easy way to get data in from sites and out for management and analysis
  • An efficient, cost-effective, all-in-one solution
  • A dedicated project manager to support you at every step

Harness the power. Eliminate the obstacles.

Why gain command?

You need it all, for studies of all shapes and sizes. And you need it all to work.

But you certainly don’t need the hassle of dealing with solutions cobbled together from multiple vendors. You don’t want to access multiple systems for different studies. And the last thing you need is to waste your time or money.

Your best option is to go full speed ahead with this powerful, efficient, integrated system. It’ll do everything you could wish for, made to order.

With you in Command, you have everything you need — integrated and optimized.

  • Full-service support from EDC and Data Management experts with 20+ years of experience
  • An easy way to get data in from sites and out for management and analysis
  • A reliable way to maintain consistency across all studies, of all sizes and complexities
  • A full-featured and fully staffed data management team and complete ecosystem
  • An efficient, cost-effective, all-in-one solution
  • A dedicated project manager and data manager to support you at every step

Our eConsent technology gives you the power to improve the entire process

Some tackle the eConsent challenge by simply turning complicated paper forms into complicated digital forms. Not Clario.

We chose to rethink the entire process and come up with an answer that meets essential needs, enhances interactions and improves the process for everyone.

Clario’s eConsent process ensures that:

  • Patients understand what they’re signing
  • Sites save time while increasing retention
  • Sponsors and CROs gain efficiency-boosting capabilities
  • IRBs base evaluations on the exact same interactions that patients have

Sound good? Read more here:

Agile, scalable and full-service management of clinical data

Clinical trials are growing more complex, and all parties are juggling complex tasks. But consider offloading the clinical data management (CDM) tasks. You might just free up valuable time for your team to focus on the important things requiring their expertise. We'll create an entire data management ecosystem for you. We've done it all before: SOPs, automated listings, coding tools, dictionaries, macros and more.

Be confident that your data is efficiently and appropriately managed by our experienced data managers. We handle the details for you — from protocol review and specification documents to electronic case report form (eCRF) creation, page review, medical coding, through tables, listings and figures (TLFs).

Whether it's helping with one component of data management or providing end-to-end data management services, we work with you to determine how best to meet your needs. And, you always have full access to your data.

We pride ourselves on our agile services. Take advantage of rapid start-up times for Clario EDC and CDM — as short as eight weeks. We plan for study milestones, conduct QC checks and work with the Study Data Tabulation Model (SDTM) structure throughout the study. This means database lock occurs earlier. And we can deliver validated SDTM datasets within 48 hours after database lock.

Combine Clario IRT, CTMS, EDC and CDM for true end-to-end support of your study and you won't have to reach out to multiple vendors and project managers for project resolution. A Clario project manager serves as your single point of contact for all software services.

Your project teams shouldn't be mired in the minutiae of data management. Our CDM services will scale across your development portfolio and are delivered by experienced industry experts — at a fixed fee — to make it easier for your budgeting.

Power. Performance. Scalability.

Built for the demands of the most complex clinical and medical research studies, Clario’s software best-in-class EDC makes no compromise on tools, capability or performance — while bringing speed, quality and efficiency to clinical study data.

Through an easy-to-use interface that earns high marks from site users, you'll quickly access:

  • A robust system that meets all regulatory guidelines and conventions, including 21 CFR Part 11 and ICH-GCP
  • World-class hosting for high-speed access to study data within a fully compliant environment
  • On-demand study data in SAS and CDISC ODM formats with self-serve exports
  • Automatic alerts — for anything ranging from SAEs to signature removals — that ensure timely, study-team response on clinical and operational issues
  • Embedded data management and review tools (for query workflows, record linking, and bookmarking, tagging and custom review status) that facilitate sponsor and CRO data review and process management

Today, more than 300 clinical trial sponsors — including all of the top 20 pharmaceutical manufacturers — depend on Clario

We'd love to discuss your EDC challenges with you