製品

eCOA

Delivering high-quality patient data with efficient deployment, simplified logistics, and expert consulting

Simplify

eCOA implementation

Streamline

quality data collection

Focus

on your patients

製品

eCOA

eCOAとIRTを統合し、試験開始から終了までのすべての被験者体験を向上させます。
製品

eCOA

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

eCOA

複雑な被験者のランダム化と治験薬供給管理。臨床試験のコマンド、およびコントロールセンターとして機能します。
Suvodaが導入された試験数
900+

その内、75%がオンコロジー、中枢神経系、希少疾患

Suvodaがサポートしている国
65

数千ヶ所にもおよぶ治験実施施設

顧客満足度
9/10

年次顧客満足度調査

Solving today’s eCOA challenges

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. 

POWERFUL AND EASY TO USE

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. その結果が、High-quality data that studies need for regulatory submission.

Efficient Implementation

Proprietary questionnaire design tool:

  • expedites questionnaire design and deployment
  • empowers study teams to seamlessly implement a single questionnaire across multiple studies 

eCOA Manager:

  • decouples questionnaire management from the system build, allowing mid-study changes if necessary
  • simplifies localization and translation implementation
  • collaborative, efficient, and agile translation management in electronic, compliant workflows

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:

  • 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 and site compliance across eCOA and IRT
シームレスなアーキテクチャ

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. これにより、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.
直感的なインターフェース

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

試験および治験実施施設チームのユーザー体験が、親しみやすく、集中できるようになることを実感できるはずです。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.

POWERFUL REPORTING

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

eCOA要件の準拠に悩みを抱える国、治験実施施設、被験者を確認する必要がありますか？治験実施施設内または自宅のすべてのeCOAデバイスの起動、バッテリーレベル、同期ステータスを確認する必要がありますか？すべてのeCOAデータの変更を監査したいですか？しかし、問題はありません。これらすべては、IRTシステムの標準レポートとしてあらかじめ設定されています。

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.

最初の発表会でシステムを見たとき、とても美しいと感じたのは不思議なことでしょうか？そして、とても使いやすい。操作の流れが、とても理にかなっていますし、ユーザーはその流れを理解することができます。特にレポート機能が素晴らしく、見たいものを自分でコントロールできます。"
Niv Alon, Head of PMO, Galmed Pharmaceuticals
関連するインサイト

IRT: 被験者とのコミュニケーションを効率的に管理し、ビジネスを成功に導く

Andrés Escallón
Vice President, eCOA Practice
 +
Jill V. Platko, PhD
Vice President, Scientific Services
 +
Emily Potz
Director, Licensing & Localization
 +
単一の臨床試験テクノロジープラットフォーム

生命の維持を目的とした臨床試験における被験者のデジタルジャーニーを強化します。

SuvodaのeConsent、IRTおよびeCOAは、臨床試験テクノロジープラットフォームの一部となっています。
クライアントサービス

広い視野、鋭い洞察力、適切なアドバイスでお客様をサポート

クライアントサービス

広い視野、鋭い洞察力、適切なアドバイスでお客様をサポート

インテグレーション

複雑な臨床試験のエコシステムにおけるシームレスなテクノロジー

インテグレーション

複雑な臨床試験のエコシステムにおけるシームレスなテクノロジー

デモはこちら

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