quality data collection
on your patients
with 75% in oncology, rare disease, and CNS
with trial sites in thousands of locations
year after year, in our annual company survey
Purpose-built to make it easier and more efficient to get quality patient outcomes data for submissions and approvals
Collecting quality data on patient outcomes is often one of the most important parts of a clinical trial. It is also challenging, and many eCOA solutions make it feel even more difficult with complicated processes, slow set up, and difficult to use tech.
Suvoda eCOA solves those problems so teams and implementations are more efficient, especially in the most urgent moments. Suvoda eCOA supports sponsors and CROs to:
- Minimize the many stresses that plague traditional eCOA solutions and delivery.
- Streamline the collection of accurate patient data for high-quality study submissions.
- Empower sites to focus more time on patients.
Sponsors can partner with Suvoda’s expert scientific consulting to guide eCOA implementation. Site teams will find the complex logistics of getting the right questionnaires to the right patient at the right time are easily and securely managed—just like the drug supply in our IRT system. And just like IRT and eConsent, Suvoda eCOA is supported by our intuitive user experience, standard and ad-hoc reporting, and customer support.
Robust functionality that drives data integrity, translation and localization, and efficient implementation.
With exceptional functionality to solve common and unique challenges of eCOA implementations, Suvoda’s eCOA tool and expert services team can do exactly what your study needs, efficiently. The result? High-quality data that studies need for regulatory submission.
Proprietary questionnaire design tool:
Centrally Managed Licensing & Localization
Repository of translated and validated questionnaires that can be used across modalities, devices, and studies
Suvoda’s in-house experts manage questionnaire licensing, translation, and localization
Established partnerships with license holders and translations vendors to simplify reusability and validation
Drive Data Integrity
Single platform and database:
A suite of standard, pre-set, and ad hoc reports:
A single eConsent, IRT, and eCOA platform to simplify outcomes data collection and submission.
To your study and site users, Suvoda eCOA and IRT administration activities will appear in a single unified interface. Why? To simplify your day to day. You can be more efficient with data that is seamlessly shared, streamlined workflows, and a process that is completely controlled. Suvoda eCOA device allocation and account set up is done easily when the IRT functionality is used during a patient’s first study visit. Our shared application logic across eCOA and IRT will enable accurate and complete data collection. And site users can proactively monitor patient compliance in real-time.Added benefits to a seamless eCOA and IRT architecture? Accuracy, integrity, accessibility. With eCOA built on the same platform as IRT, sponsors reduce manual data entry at sites, creating an always-on, single source of truth. This reduces errors, increases accuracy, increases data integrity, and delivers real-time visibility to patient data that can inform drug supply.
Digital experience that makes eCOA equally simple for clinical trial professionals and their patients.
Study and site teams will find the user experience to be calming, familiar, and focusing. That’s because we based it on the minimalist look and feel, intuitive navigation, and patient-centric processes of our proven IRT system, implemented in over 1,000 trials worldwide.
The collection of clinical outcomes data is an activity increasingly in the hands of patients, often at home, without supervision, rather than by trained clinical trial professionals. So, we’ve taken added steps to ensure that patients find their interactions with eCOA questionnaires and diaries to be simple. Even the initial setup of their eCOA device at the site through a shared workflow with our IRT system is managed through a simple, secure, QR code download. It’s an elegant way to give patients a better clinical trial experience—and produce higher quality outcomes data.
Real-time eCOA status at your fingertips through Suvoda IRT’s pre-set and ad-hoc reports.
Do you need to see what countries, sites, or patients are struggling to comply with eCOA requirements? Are you looking to determine the activation, battery level, and sync status of all in-clinic or at-home eCOA devices? Will you want to perform an audit of all eCOA data changes? No problem. They—and others—are all standard, pre-set reports in our IRT system.
Even better, our much-loved IRT ad-hoc reporting function is available for eCOA as well, so you can build your own analyses, on the fly. Though it’s our software, it’s your data. Our goal is to give you what you need to make informed decisions, quickly.
Vice President, eCOA Practice
Jill V. Platko, PhD
Vice President, Scientific Services
Director, Licensing & Localization
Director, eCOA Operations
Director, eCOA Services Delivery