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StudyOS guided demo

See StudyOS in action

Design and run a study programme: protocol development, feasibility, budget and sponsor oversight.

Illustrative screens with sample data — no sign-up, nothing to install, and no real customer records. Share this link with anyone.

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Step 1 of 4

Sponsor oversight

Programme-level view across studies: milestones, spend, risk and the decisions waiting on the sponsor.

StudyOS / Oversight

Programme oversight

Active studies

4

2 enrolling

Milestones at risk

2

site activation

Budget used

58%

on plan

Open decisions

3

sponsor action

What makes StudyOS different

The parts a generic document system or spreadsheet cannot do

Sponsor oversight in real time

Enrolment, query ageing, deviation rates and site performance update as sites work, instead of arriving in a monthly status deck.

eTMF with completeness scoring

The trial master file scores itself against the expected artefact list, so inspection gaps are visible while they are still cheap to fix.

Priced for device studies

Packaging is built around device trials — per-study and per-site tiers, not per-patient CRO pricing — with an ROI estimator that shows the comparison in writing.

Shared spine with ClinicalOS

Sites, subjects and safety events are the same records the clinical team already uses; sponsor oversight is a view, not an integration project.

Answers, not a sales call

The ten questions everyone asks about StudyOS

Answered here in full. Anything else, ask below and you get an immediate answer.

Sponsors and study teams running device studies: protocols, feasibility, site oversight, milestones and budget in one operational view.

Answered automatically from Qevatrix product documentation. No email required.

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