CLININFO EPRO
Patient-Friendly Experience

Simple, intuitive ePRO designed to maximize patient engagement and adherence.

Built-in PROs & Scoring

Licensed PROs with built-in scoring, ready to use and compliant by design.

eConsent Made Easy

Flexible, fully digital eConsent adapted to decentralized and hybrid study models.

Seamless eCRF Integration

Real-time data synchronization and centralized control.

Our aim

Increase patient engagement by providing a simple, intuitive, and accessible ePRO solution that encourages consistent participation throughout the study.

Our offer

Quick Login

Fast access via QR code or unique credentials for immediate use.

Multi-Device

Accessible on mobile, tablet and desktop for ultimate flexibility.

Simplified Interface

User-friendly, multilingual design to make participation easy and intuitive.

Advanced Profiles

Support for different user roles, including caregivers, parents, or child participants.

Timely Data Capture

Control over questionnaire display, entry time windows, and response visibility.

Smart Reminders

Customizable notifications and alerts to boost adherence and engagement.

Our aim

Offer a wide range of pre-configured licensed PROs, with scoring and calculations, to ensure compliance with license requirements and rapid deployment.

Our offer

Licensed PROs

Access a large library of validated PROs, ready to use and fully compliant.

Study-specific PROs

Simple and fast implementation of custom PROs tailored to your study.

Dynamic Layouts

Customizable pages and fields to make questionnaires simple and engaging.

Automatic Scoring

Built-in scores and calculations instantly computed.

Controlled Entry

Manage whether participants can complete questionnaires in multiple sessions.

Flexible Requirements

Set optional or mandatory questions to maximize participant comfort.

Our aim

Enable easy, fully digital consent that can be implemented quickly and adapted to any study content, supporting decentralized study models.

Our offer

Fully Digital and Customizable

Interactive consent forms with customizable content and embedded images.

Flexible Workflows

Multiple documents, optional choices, PI signature, caregiver approvals.

Seamless Integration

Automatically connected with ePRO and eCRF, reducing errors and rework.

Version Control

Amendments, re-consent processes and fully compliant audit trails.

Paper Alternative

Paper alternative option, allowing patient-level or site-level choice.

Country-Specific Consent

Multilingual support and country-specific documents for a smooth implementation.

Our aim

Integrate ePRO into the global study ecosystem, with real-time data access, scheduling tied to study visits, and controlled alternative entry options.

Our offer

Real-Time Access

Instant view of ePRO data, enabling proactive decisions and monitoring.

Controlled Roles

Define who can view or enter PRO data, ensuring security and data integrity.

Smart Scheduling

ePRO questionnaires aligned with study timelines, adapting to any date change.

Alternative Entry Processes

Flexible data capture on paper or other methods to maximize data collection.

Data Merged

ePRO data merged seamlessly with the eCRF for centralized analysis and reporting.

Centralized Patient Management

Simple management of patient accounts, with personalized emails by sites.

Reliable and Flexible ePRO

Flexible, secure, and patient-friendly solutions that adapt to any study design.

Customizable Experience

Quickly adapt questionnaires and workflows to any study design and participant condition.

Our aim
Deliver a fully flexible ePRO solution that can be rapidly implemented, tailored to any study type, and accommodate multiple participation modes.
Key Capabilities
  • Quick study deployment using ready-to-use configurations and templates.
  • Easy adaptation of workflows, time points and questionnaires without technical complexity.
  • Multiple participation modes supported: digital, paper, or assisted entry.
  • Customized site tools enabling teams to support patients efficiently and consistently.

Data Privacy

Designed to meet the highest data protection standards, ensuring privacy, security, and regulatory compliance.

Our aim
Provide a secure and compliant environment that protects patient data, enforces strict access control, and fully respects regulatory requirements.
Key Capabilities
  • Two operating modes: with or without collection of identifiable patient data. including QR-code access.
  • Data encrypted both in transit and at rest.
  • Technical isolation ensuring unauthorized access is structurally prevented.
  • Full compliance with GDPR, HIPAA, and industry standards.

Everyday Patient Experience

A patient-first experience designed to reduce burden, improve adherence, and fit real-world use.

Our aim
Integrate ePRO into participants' daily routines with timely reminders, device compatibility, and flexible entry windows to maximize adherence and data completeness.
Key Capabilities
  • Customizable SMS and email reminders sent before or after due dates to support adherence.
  • Instant access on any device, no installation required, with native compatibility for connected tools.
  • Clean interface highlights only relevant tasks, avoiding unnecessary prompts and showing upcoming deadline.
  • Expert-designed interfaces to simplify completion, reduce burden, and prevent patient confusion or errors.

Advanced ePRO Tools

A comprehensive set of flexible, built-in capabilities to enhance patient engagement, support complex study designs, and ensure operational reliability.

Operational Reliability

A robust platform designed to ensure stability, performance, and continuity throughout the entire study lifecycle.

Advanced Study Designs

Support complex study designs including cohort-based PROs, basket or umbrella studies.

Interoperability & API Flexibility

Seamlessly integrate third-party ePRO solutions or replace modules via APIs to fit your existing ecosystem.

Eligibility-Driven ePRO

Use ePRO responses to dynamically determine patient eligibility and drive hybrid study designs combining eCRF and ePRO logic.

Sponsor & CRO Control

Provide full visibility and control over study progress, PRO completion, and data quality across sites and cohorts.

Long-Term Study Support

Built to support long-duration studies with evolving protocols, amendments, and ongoing operational needs.

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Complete Clinical Software Ecosystem

A wide range of seamlessly connected solutions to cover every aspect of your clinical study.

eCRF

Rapidly deploy and customize your study data capture.

ePRO

Capture patient-reported outcomes efficiently and remotely.

IWRS

Simplify randomization and study drug management.

CDMS

Centralize and clean study data in real time.

eTMF

Manage essential documents securely and compliantly.

CTMS

Track study progress and monitoring easily.

Regulatory Compliance

Our solution ensures full regulatory compliance, with secure, auditable, and reliable clinical data management.

FDA GCP GDPR HIPAA
ISO HDS SOC

See Your Study Come to Life

Discuss with our experts about your study, test a custom sandbox, and see how our solution can be tailored to your needs.

Request a Demo