Clinical trial Management System

Clinical Trials

Medicus Research brings form building, data capture and trial oversight together in one GCP-aligned platform - built for NHS research teams, academic CTUs and small CROs.

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Clinical trials, managed from one place

Managing an investigator‑led trial involves coordinating forms, data, queries, tasks, and teams, often across multiple systems. Medicus Research simplifies this by bringing everything into one platform with one login and one audit trail.

Key Features and Benefits

Drag-and-drop eCRF

Design and preview forms in real time, no technical support needed. Build the data capture you need for your trial.

Version‑locked forms

Every form version is immutable and preserved, with a complete audit trail from first draft through to final submission.

Role-specific dashboards

Nurses, data managers and chief investigators each see what matters to them, tailored to how they actually work rather than a generic view.

Task and query handling

An integrated system so nothing gets lost between teams. Queries are raised, tracked, and resolved without leaving the platform.

End-to-end recruitment

From candidate identification through to enrolment - the full recruitment journey in one place, with clear oversight at every step.

Single audit trail

Everything uses a single login and audit trail, with no need to reconcile data across systems.

Built to fit your workflows

Already using Medicus?

Organisations already running Medicus can extend into clinical trials without adopting a separate system. Existing integrations carry over, reducing manual entry and connecting clinical workflows that are currently siloed.

Using another EDC?

For sponsors or CROs using other EDC platforms, Medicus Research supports standard data export formats, so captured data flows into any central EDC for aggregation and regulatory submission, without any lock in or duplication

NHS or academic setting?

Medicus Research works as a fully standalone product. NHS research teams, academic CTUs, and small CROs get GCP-aligned trial management without enterprise complexity or enterprise pricing.

Benefits

Automate data collection

Minimise manual data collection efforts with integrations to other hospital systems including EPR; PAS or Lab systems via HL7 or FIHR sharing. This improves data accuracy and consistency.

Quality improvement

Easily manage quality improvement initiatives and track performance and outcomes against patient data.

Clinical intelligence

AI powered insights, to unlock the value in your data. From predictive analytics to natural language querying of the data, easily navigate and find actionable insights.