Visual principal de GenomIT Healthtech

Evidentia

Real World Evidence from clinical question to actionable knowledge

Evidentia combines a flexible data capture and analytics platform with full-service support for Real World Evidence projects.

RWE service & end-to-end guidance

We offer more than a platform

A Real World Evidence project does not start with a form and does not end when a database is completed. Our team can support every stage, combining technology, medical expertise, and analytical capability.

END-TO-END METHODOLOGY

7 Guidance phases
  1. Objective and protocol definition

  2. Form and variable design

  3. Platform setup

  4. Hosting and operations

Data continuity
  1. Data capture and control

  2. Visualization and analysis

  3. Results interpretation

Dynamic forms & CRF

Much more than forms

Adaptable logic & complex variables

Evidentia enables dynamic CRFs tailored to each study logic, supporting field types, validations, conditional rules, and workflows beyond generic form tools.

Workflow & advanced validation

Modeling complex information structures and clinical approval flows beyond generic survey tools.

CRF builder interface with dynamic logic and validation rules
Profiles & permissions

Each person accesses exactly what they need

Granular access by responsibility

The platform supports profile-based permissions for each responsibility:

Physicians and researchers

Data analysts

Pharmacovigilance specialists

Administrators

Custom roles per project

Roles and permissions panel for clinical and data teams
AI-assisted structuring

Less time entering data. More time analyzing.

Less manual load, more clinical analysis

Evidentia uses AI to transform unstructured information into structured data from PDFs, Excel files, text reports, and clinical documents.

Automated extraction from PDFs and spreadsheets

Configurable quality rules per variable

AI-assisted data structuring and validation workflow
Conversational analytics

Ask your data directly

Ask your data in natural language

Users can query project information in natural language instead of navigating multiple tables and filters.

What was the response rate in patients older than 65?

How many grade 3 adverse events were recorded in the last six months?

Compare outcomes between groups A and B.

Chat interface for clinical data questions
Operational dashboards

From data to decisions

Decision-ready visibility

Evidentia enables interactive and customizable dashboards to visualize indicators, apply filters, and explore project dimensions.

Cross-study KPI tracking

Segmented filters by cohort and period

Clinical dashboard with key indicators and filters
Security & compliance

Sensitive data requires robust infrastructure

Clinical-grade controls by default

Two-factor authentication (2FA)

Role-based access control

Daily backups

Auditability and access traceability

Protection of sensitive information

Secure infrastructure

Regulatory framework

Architecture aligned with GDPR and HIPAA requirements as needed by each project

Operational support

Support throughout the entire project

Companion team throughout the project

Users have access to a help desk for operational support. Behind Evidentia there is a team that understands both technology and medical-scientific requirements.

Follow-up on field incidents and data quality

Functional and technical support for all profiles

Operational support and monitoring panel for RWE projects
Clients & social proof

Clients and social proof

Frequently asked questions

How long does implementation take?

It depends on the scope of the project. Timelines are shaped by the number of forms, the complexity of validations and conditional rules, integrations with other sources, and how far the support goes: platform only, or also protocol, operations, and analysis. A study with CRFs already defined goes live sooner than an end-to-end project with its own roles, approval flows, and dashboards. The schedule is set with the team at the start, once the study design is clear.

Can it be customized per study and role?

Yes. Each study can have its own CRFs, with field types, validations, conditional rules, and workflows adapted to its logic. Permissions are defined by responsibility — physicians and researchers, data analysts, pharmacovigilance specialists, administrators, or other project roles — so each person can see and edit only what they need. Dashboards and natural-language queries are also tailored to that study's indicators and questions.

How do you handle security and compliance?

Evidentia includes two-factor authentication, role-based access control, daily backups, and access traceability. The infrastructure is built for sensitive clinical information. When a project requires it, the architecture is aligned with international data-protection standards such as GDPR and HIPAA. A help desk also supports day-to-day operations and understands both the platform and the medical and scientific context.

Planning a Real World Evidence project?

We can help from protocol definition to analysis and interpretation.

Let's discuss your RWE project