Divolvi automates end-of-trial device recovery — AI outreach to your sites, prepaid labels on your own carrier account, device valuation, and FDA/NIST compliance certificates. One pipeline, zero spreadsheets.
Six moving parts of device recovery, unified into one automated pipeline.
AI email campaigns reach your site contacts at trial end, chase every device, and read the replies straight back into the pipeline. No rep time, no spreadsheets.
Prepaid FedEx labels on your own carrier account, with pickup scheduling and tracking. Shipping cost stays yours. UPS coming soon.
Every returned unit is graded and valued on arrival. AI market valuation backed by live web data.
FDA / NIST PHI-wipe attestation generated per device, audit-ready by default.
A monthly subscription metered per active site, plus a per-recovered-device fee. All reconciled and invoiced automatically.
Outreach, transit, receipt, valuation and compliance. Every trial, site and device in one real-time view.
One automated pipeline moves every device from the site back to your warehouse, and documents each step.
At trial end, the AI Coordinator emails each site contact and works every reply until the devices are ready to ship.
A prepaid FedEx label is generated per box on your own account, and carrier pickup is scheduled.
Every box is tracked door to door, with status flowing into one live pipeline.
Operations confirms each returned device in hand at your warehouse.
Each unit is graded and valued on arrival with AI market valuation.
An FDA / NIST PHI-wipe certificate is generated per device — audit-ready.
Divolvi fits both sides of Clinical Trial logistics: The strategic portfolio view and the daily action queue.
Trials, sites, recovery status, device valuations and compliance across every study — the strategic weekly view, with reports and financials.
A tactical action queue: which sites to chase, which boxes to label, what's in transit, everything scoped to the sites you own.
Every recovered device leaves a documented chain of custody from the site contact's first reply to the final PHI-wipe certificate.
Every recovered device gets an FDA / NIST 800-88 PHI-wipe certificate, generated per device.
Every site edit, deployment, shipment and receipt is captured in an immutable audit trail.
Each organization's trials, sites and devices are fully partitioned — data never crosses tenants.
Run the full recovery pipeline on your own trials and sites — free for 90 days. Book a demo and we'll get you set up.