Our Products

eCOA for confident clinical trials

Suvoda eCOA supports ePRO and eClinRO in one purpose-built system designed for trial complexity. Improve data accuracy, support patients and sites, and maintain operational control from trial planning through study close.
Reduce operational risk
< 10

data clarification forms per trial on average

Keep your trial on track
100%

on-time eCOA deployment

Improve usability
100%

of testers had an easy time navigating Suvoda eCOA 

Our Products

eCOA

Unify eCOA and IRT systems and elevate your experience from trial start to study completion, with Suvoda
Our Products

eCOA

Suvoda launches eCOA-specific design toolkit as solution moves to second phase of early adopter program

 

Suvoda's patented eCOA supports sponsors and CROs

Deploy eCOA with confidence

Reduce clinical trial operational headaches

Capture reliable patient data

Let sites focus on care

Backed by expert teams and accelerated questionnaire delivery.

Flexible technology architecture that adapts to protocol needs.

 

Accurate, audit-ready outcomes that support high-quality submissions.

Site teams spend more time with patients instead of managing technology.
OUR PRODUCTS

eCOA

Our advanced patient randomization and trial supply management system. Your clinical trial command and control center.
Trials conducted
900+

with 75% in oncology, rare disease, and CNS

Countries supported
65

with trial sites in thousands of locations

Client satisfaction
9/10

year after year, in our annual company survey

Solving today’s eCOA challenges

Purpose-built to deliver quality patient outcomes data, more efficiently. 

Collecting quality data on patient outcomes is critical, but traditional eCOA solutions complicate data collection, lack questionnaire reusability, slow set up, and are difficult to use. Suvoda eCOA solves these problems so teams and implementations are more efficient, especially in the most urgent moments.

Sponsors get guidance from Suvoda’s scientific and licensing experts, while site teams can effortlessly manage questionnaire delivery with the same precision as drug supply in our IRT system. Supported by an intuitive interface, flexible reporting, and dedicated customer service, Suvoda eCOA makes complex operations simple and reliable.

Suvoda eCOA was incredibly easy for our patients to use; we had an increase in patient compliance in completing PRO questionnaires, as compared to previous studies with other eCOA providers.”
Catherine Munera, Vice President of Biometrics, Cara Therapeutics
Related Insights

eCOA Buyer's eBook

Choosing an eCOA partner you can trust: How Suvoda addresses 5 common industry challenges

eCOA FAQs

View the full eCOA FAQ list →

POWERFUL AND EASY TO USE

Robust functionality that drives data integrity, streamlined questionnaire licensing and localization, and efficient implementation.

With exceptional functionality to solve common and unique challenges of eCOA implementations, Suvoda eCOA and our expert scientific, licensing and localization, and operations services teams can do exactly what your study needs, efficiently. The result? High-quality data that studies need for regulatory submission.

“Suvoda was an eCOA thought partner, helped us understand what the system was doing and could be doing—and what we should be doing."
- Senior Director, Clinical Operations 

 
 

Efficient implementation

Patented questionnaire design tool, Suvoda Questionnaire Design Language: 

  • Expedites questionnaire creation, translation, layout, and deployment 

  • Empowers study teams to seamlessly implement a single questionnaire across multiple studies

Suvoda’s Questionnaire XD:

  • Decouples questionnaire management from the system build, so localization can start earlier and allowing mid-study changes if necessary

  • Simplifies localization and translation implementation

  • Enables collaborative, efficient, and agile translation management in electronic, compliant workflows

  • Patients complete eCOA in the Suvoda patient app - a single intuitive app where patients can schedule visits, submit receipts and receive payments, answer questionnaires, view travel details, and receive reminders.

     

Support for BYOD (bring your own device), provisioned device, and hybrid models

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. Translation vendors work directly in the system to streamline localization

  • Established partnerships with license holders and translations vendors to simplify reusability and validation

Drive data integrity

Single platform and database:

  • Enables seamless flow of information between IRT and eCOA

  • Reduces duplicate data entry

  • Supports clean data transfers to EDC

  • Allows control over patient eligibility, randomization, stratification, and dose management, based on questionnaire inputs

  • Allows mid-study analysis

  • Delivers an inspection-ready and submission-friendly archive

A suite of standard, pre-set, and ad hoc reports:

  • Provide real-time visibility to patient data across eCOA and IRT

Real-time data workflow support:

  • Collect data seamlessly from connected medical devices like glucometers
  • Gate access to ClinRO assessments based on rater training and certification
PATENTED ARCHITECTURE

Built on our single clinical trial technology platform, Suvoda eCOA and IRT 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 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.  

“The process was almost seamless! Better than other vendors I have previously worked with. The team is consistently responsive, knowledgeable, and dedicated to our study success."  

 Senior Clinical Trial Manager 

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. 

INTUITIVE INTERFACE

Digital experience that makes eCOA equally simple for clinical trial professionals and their patients.

Study and site teams, as well as their patients, will find the user experience to be intuitive, easy to navigate, and well-designed, as validated through usability testing conducted by RWS Life Sciences.1 That’s because we based it on the minimalist look and feel, straightforward navigation, and patient-centric processes of our proven IRT system.

“…With [the RWS usability] certification, sponsors can feel confident that Suvoda eCOA is easy to use for study participants while ensuring the integrity of the data captured.”  

Chryso Hadjidemetriou, PhD, Survey Research Analyst, RWS Life Sciences 

The collection of clinical outcomes data is an activity increasingly in the hands of patients, often at home, to complement outcomes data reported by observers and clinicians. So, we put the system user at the center of our eCOA design process to ensure that patients, observers, and clinicians find their interactions with eCOA questionnaires and diaries to be simple. Even the initial setup of the 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.

1. Source: Hadjidemetriou, C., Poepsel, T. (2023). "Solidifying Usability Testing Guidelines for ECOAs From the Patient Perspective". Value in Health: Volume 26, Issue 12.https://www.valueinhealthjournal.com/article/S1098-3015(23)05591-2/fulltext.
POWERFUL REPORTING

Real-time eCOA status at your fingertips through Suvoda IRT’s pre-set and ad-hoc reports.

Do you need to see how specific countries, sites, or patients are complying 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. 

“I would recommend Suvoda because they are honest about capabilities and timelines, always deliver and maintain a quality product, and provide consistent, high-performing project management and technical support.” 

Suvoda Customer Satisfaction Survey 2023 

At the very first presentation when we saw the system, is it strange to say that it seemed very beautiful? And very easy to use. The flow makes a lot of sense. Users can figure it out. The reports in particular are great, and I can control what I want to see.”
Niv Alon, Head of PMO, Galmed Pharmaceuticals

Peter Bennett
Vice President, Specialty Sales
+
Andrés Escallón
Vice President, eCOA Practice
 +
Emily Potz
Director, Licensing & Localization
 +
Roger Vaillancourt
Director, eCOA Operations
+
A UNIFIED CLINICAL TRIAL PLATFORM

Powering the patient's digital journey in life-changing clinical trials

Embrace today’s clinical trial complexities with a market-leading, real-time software platform to drive confident decisions and calm action.
PATIENT APP

Simplify patient participation

A convenient app where patients can answer their questionnaires and fill out daily diaries.
Client Services

Broad perspective, keen insight, and calm guidance

Client Services

Broad perspective, keen insight, and calm guidance

Integration

Seamless technology in complex trial ecosystems

Integration

Seamless technology in complex trial ecosystems

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