B2B pharma & life sciences data infrastructure

RWE data capture and patient support beyond the pill.

Capture real-world patient behavior between visits. Optimize clinical trial retention, PSPs, and market access with FHIR-native markers.

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Zero-Friction Deployment: Mential operates strictly at the cohort level—completely outside EU MDR (2017/745) Software as a Medical Device scope.

Across the drug lifecycle

Four products, one behavioral engine

Clinical Operations / CROs / Trial Managers

Trial retention & adherence intelligence

Predict patient dropouts before they happen. Capture real-world behavioral signals between protocol visits to keep trials on schedule.

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Automated dropout risk scoring by patient cohort.

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Between-visit PROs/PROMs and burden tracking.

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Interoperable FHIR R4 metrics for EHR integration.

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Save up to €18,000 per replacement patient and avoid €51,000/day Phase III delays.

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Zero-Friction Deployment: All intelligence is generated strictly at the cohort/segment level—never as individual clinical decision-making. Mential operates completely outside EU MDR (2017/745) Software as a Medical Device scope.

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“Beyond a single average.”

Beyond the four products

Beyond a single average.

Who responds best

distinct subgroups with distinct response trajectories

Value-based pricing

outcomes-based agreements when a subgroup shows superior benefit

Dosing patterns

real-world dosing patterns observed across the cohort

Persistence forecasting

project persistence and volume per profile, not one average

Combination signals

residual-symptom patterns correlated with combination-therapy usage in the cohort

verified_user

Zero-Friction Deployment: Mential operates strictly at the cohort level—completely outside EU MDR (2017/745) Software as a Medical Device scope.

How it works

From methodology to evidence.

01

Design

We apply the methodology to your study population or cohort.

02

Capture

Multimodal behavioral data, structured to FHIR / SNOMED / LOINC.

03

Evidence

Exploratory or secondary endpoints and publication-ready datasets.

Trial participant reporting symptoms and treatment experience in the Mential app
Trial participant's check-in agenda and mood log in the Mential app
Data Governance

Compliant with Industry Standards

Interoperability by Design

Native FHIR R4 mappings with SNOMED CT and LOINC catalogues. Easy integration into EHRs and clinical data lakes.

Enterprise Security & Privacy

GDPR compliant, signed DPIA, with 100% European Union data residency.

Non-SaMD Regulatory Path

Analyzes aggregated behavioral markers at the cohort level, eliminating medical device regulatory friction.

Engagement

Why patients and caregivers stay engaged

Meaningful support in exchange for continuous participation — the same engagement that keeps your trial retention high and your PSP data audit-ready.

Trusted Health Education

Personalized, validated information on disease and treatment — designed to support protocol adherence and reduce early dropout

Low-Burden, High-Fidelity Reporting

Voice, text, images or short questionnaires — cleaner real-world data with less patient burden

Caregiver-Inclusive Design

Proxy reporting and guidance for elderly or paediatric patients — protecting retention in the cohorts hardest to keep engaged

1,700+
FHIR markers
FHIR · SNOMED · LOINC
Submission-ready
EEA
GDPR-compliant
Get started

Accelerate your RWE strategy today

Schedule a meeting with our Life Sciences team to evaluate Mential for your pipeline or PSPs.

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Funded by

This website/project is part of the Recovery, Transformation and Resilience Plan, funded by the European Union – NextGenerationEU.