Expedite cycle times, enhance quality and ensure compliance with a clinical trial optimization platform built for sponsors, CROs, AROs, sites and core labs. Judi connects your stakeholders, data, actions and decisions to build trial momentum while driving cost efficiency. By orchestrating your workflows and governing AI models, Judi ensures every output is traceable and every decision defensible.
Most clinical trial work still runs on email, spreadsheets, shared drives and homegrown solutions.
Each handoff introduces the risk of delay, protocol deviation and an incomplete study record.
Reviews get stuck in inboxes and trackers. You don’t notice the bottleneck until it is already costing you.
Sites and teams interpret protocols differently. This fragmentation creates avoidable deviations.
Decisions, evidence and data are scattered. You are left without a defensible study record.
DEVIATIONS
related to enrollment
decisions.
LOWER COST
per monitoring visit, cut
from $3,500 to $500.
EXPEDITED
cycle time from
report to decision.
ANALYZABLE
images delivered
right the first time.
Unifying your study operations on one platform drives cross-functional efficiencies.
Configuring multiple workflows moves you past individual wins to unlock a new level of clinical trial optimization.
Enroll the right patients from the start. An inaccurate eligibility decision is a protocol deviation you can’t undo.
Verify source data without expensive site visits. Lower your monitoring costs while data review keeps pace with your trial.
Remove manual effort from DSMB coordination. Protect patient safety and keep the blind intact.
Deliver complete, analyzable images on time. Mask all protocol-defined identifiers at the image source.
Systems like your EDC, CTMS and ePRO were built to capture data. Judi does the work they were never built for.
Your systems stay. The workarounds go.
Put your data to work. Judi turns passive, siloed data into real-time operational momentum. Connect your systems to protect timelines, eliminate manual errors and maintain an inspection-ready audit trail.
Weeks, not months. Backed by our experience across 2,000+ clinical trials, we rapidly configure Judi to your specific trial and operational plans.
Sponsors, CROs, AROs, labs and sites in one unified workspace. Judi guides the actions and handoffs between them. Everyone works from the same real-time view, so next steps and deadlines are clear.
SOC 2 Type 2 examined every year since 2021, most recent report with no exceptions.
Four recur across trials: reviews that sit in inboxes with no visible owner, source data verification that waits on a site visit, committee decisions that stall for want of a complete data package, and records assembled after the fact rather than captured as the work is done. Each one adds days to database lock. Judi removes the wait by putting the work, the evidence and the record in one place.
Database lock waits on the slowest review. Sponsors and CROs shorten that path by moving reviews, queries and decisions onto one platform where every step is captured as the work is done, so nothing sits unnoticed and nothing gets reconstructed at the end. On Judi, enrollment decisions have gone from nine days to 2.1 and endpoint cycle times from 113 days to 30.
Start with the systems that already own the data and connect to them rather than re-entering. Judi connects to EDC, CTMS, ePRO, safety databases, identity providers and imaging archives through an open API configured to your trial, so participant and visit data flows in without duplicate entry. Every API call and system change is captured in the audit trail alongside the human actions.
No. Judi and your EDC do different jobs. The EDC is the system of record for structured trial data. Judi runs the work around that data: the handoffs between teams and organizations, the reviews and decisions made on the evidence, and the record of what happened, when, by whom and why. Judi connects to EDC, CTMS and ePRO systems through an open API, configured to your trial, so participant and visit data flows in without re-entry.
Judi can support any and all clinical trial workflows, each configured to the protocol and project plans it serves, on one validated platform. Most trials run eligibility, imaging, DSMB, remote source data verification and adjudication. Also running today: user qualification, IRB, screening coordination, document development, 24/7 medical monitoring, clinical safety, protocol deviations and steering committee. We continually roll out new workflows. Need a workflow that isn’t here? If you can draw it, we can build it.
Judi is designed and validated to support your Part 11 compliance, covering electronic records and signatures, audit trails and access controls. No Part 11 certification exists for any vendor. Judi is SOC 2 Type 2 certified, examined annually since 2021, and validated as a GAMP 5 Category 4 configured product. Judi is hosted on AWS with content encrypted in transit and at rest.
Judi governs every AI model working in your trials, ours, native and third-party. Nothing acts without permission, consequential actions pass through approval gates, and every output and every step lands on the same audit trail as the rest of the trial. Judi records who authorized every action, whether it was permitted, and how the decision was reached.
Judi is the layer where the work gets done and recorded. Sponsors and CROs run their trial processes on it. Organizations building AI capabilities deliver them through it, so every model output is permissioned, reviewed and traceable.
Yes. Judi is SOC 2 Type 2 certified and holds active certification under the EU-U.S. Data Privacy Framework, including the UK Extension and the Swiss-U.S. DPF. The SOC 2 examination is an independent CPA review of the design and operating effectiveness of our security controls, performed every year since 2021, with no exceptions noted in the most recent report. Judi operates as a data processor and business associate on behalf of sponsors and CROs, and is designed and validated to support your 21 CFR Part 11, HIPAA and GDPR obligations, covering electronic records and signatures, audit trails and access controls. Trial data is collected, processed and reviewed in a validated, access-controlled platform, with every action captured in a timestamped audit trail. AG Mednet supports client security questionnaires, vendor assessments and audits as part of standard engagement, and can share evidence on request.