Our services

Real-world evidence, at scale

We design and deliver RWE studies that generate robust, meaningful evidence from real-world settings — using validated tools, wearables, and remote data collection to capture outcomes as they happen.

Real-world evidence

Evidence that reflects the real world

Real-world evidence studies demand flexibility, scale, and precision. We support sponsors, academic institutions, and industry partners in generating high-quality RWE through open-label trials, longitudinal observational studies, and technology-enabled data collection — all delivered remotely.

Our remote-first infrastructure means participants can be recruited and followed up from anywhere in the UK, with validated outcome measures, wearable integration, and at-home testing built in from the start.

Study types

Open-label trials, longitudinal observational, patient registries, and pragmatic studies

Data sources

ePRO, wearables, cognitive assessments, at-home biomarker testing, and validated questionnaires

Compliance

GCP-aligned operations, full GDPR compliance, and UK-based data residency

Delivery

End-to-end management — study design through final analysis and reporting

What we handle

From study design to final report, we manage every operational aspect of your RWE study.

Study design & protocol

RWE-specific study design, outcome measure selection, protocol and analysis plan drafting, ethics submission, and study registration.

Remote data collection

ePRO and eDiary capture, validated cognitive and patient-reported outcome measures, wearable device integration, and at-home biomarker testing kits.

Monitoring & oversight

Real-time data quality monitoring via Trialflare, remote participant support, query management, and protocol deviation tracking throughout the study.

Analysis & reporting

Statistical analysis to the pre-agreed SAP, benefit-risk assessment where required, and a comprehensive final study report ready for publication or regulatory review.

How an RWE study comes together

A typical real-world evidence study with Comet Clinical follows four clear phases.

1

Research question & design

We work with you to define the research question, select appropriate outcome measures and data sources, and develop a robust study protocol and analysis plan.

2

Ethics & setup

Ethics submission and approval, EDC build and validation, recruitment strategy activation, and participant onboarding via digital eConsent.

3

Data collection & monitoring

Remote data capture via ePRO, wearables, and at-home testing. Continuous data quality monitoring with real-time query resolution and participant support.

4

Analysis & reporting

Database lock, statistical analysis per the SAP, final report preparation, and archiving — with full audit trail maintained throughout.

Ready to discuss your RWE study?

Tell us about your research question and we'll talk through how Comet Clinical can design and deliver it.

Schedule a consultation