Judi is the clinical trial optimization platform built for the AI era. It’s where the work of your trial gets done – faster and better – across sponsors, CROs, AROs, core labs and sites. Judi orchestrates the execution of your workflows and governs AI models, so every output is traceable and every decision defensible.
Every trial depends on decisions made across sponsors, CROs, AROs, sites and committees. When those handoffs happen in email, spreadsheets and shared drives, decisions sit and wait and work gets lost. The risk lands on your data, timelines, budget and your ability to prove it all at inspection.
Work stalls between teams. Reviews back up, queries go unanswered and database lock slips.
Rework, manual tasks, duplicate effort and disconnected systems compound across the trial. Every inefficiency lands on the budget.
The protocol gets applied differently across the trial. Inconsistent data undermines every decision that depends on it.
Decisions, evidence and ownership scatter. The full record of what, when and why no longer exists.
Every trial runs on decisions made across sponsors, CROs, sites and committees. When those handoffs happen in email, spreadsheets and shared drives, decisions sit and wait, work gets lost, and the risk lands where it matters most: on your patients, your data, your timelines, your budget and your ability to prove it all at inspection.
Work stalls between teams. Reviews back up, queries go unanswered, and database lock slips.
Rework, manual tasks, duplicate effort and disconnected systems compound across the trial. Every inefficiency lands on the budget.
The protocol gets applied differently across the trial. Inconsistent data undermines every decision that depends on it.
Decisions, evidence and ownership scatter. The full record of what, when and why no longer exists.
From study startup to database lock, every workflow in your trial runs in Judi, configured to your protocol and operational plans. Every action, decision and handoff is captured as the work happens, across teams and organizations, in one audit-ready system. When an AI application takes a step in that process, it takes it under the same permissions and leaves the same record as anyone else.
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.
Reach defensible endpoint decisions faster. Expedite case processing and deliver high quality dossiers to adjudicators.
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.
Document user training activities in one place. Training status captured as it happens.
Running a clinical trial is hard. Fast, chaotic and one bad bounce from losing control. Judi gives you guardrails. Every decision, every document, every data point stays in play, moving in the right order and at the pace you set.
Judi provides a dual approach to intelligent clinical trial operations. We deliver native AI tools built directly into the platform—like AI-assisted PHI redaction—and we provide a single governance framework that oversees both our own native tools and any external, proprietary or third-party models you bring to your trial.
Judi governs all AI the same way: the models built into Judi and the models you bring. Each one is treated exactly like a human team member. Every model is assigned to specific duties with defined steps, managed under the same permissions and tracked in the same audit trail. Judi builds in AI guardrails and human-in-the-loop oversight. The technology handles the heavy lifting; humans own the decision.
Regulators hold the sponsor accountable for the entire trial, even work delegated to other parties. Without centralized visibility, tracking compliance across CROs, AROs, sites, labs and vendors is nearly impossible. Judi centralizes oversight, so the work you are accountable for is work you can see.
FDA and EMA both expect validation and audit trails behind AI-assisted decisions. Governance has to exist before AI is deployed, or outcomes are not defensible. Judi treats every AI model, ours, proprietary or third-party, like a team member: defined duties, set permissions and a person on every automated step.
Judi unifies disparate systems and stakeholders into configurable workflows. Sitting at the center of your trial, the platform provides real-time, trial-wide visibility. By unifying team workflows, Judi delivers both comprehensive oversight capabilities and AI governance to keep your trial compliant and audit-ready.
Legacy trial processes are manual, siloed and prone to costly delays. With Judi, work in progress stays visible, cycle times stay short and bottlenecks never get the chance to form. As you centralize more workflows within the platform, the benefits multiply across your portfolio, turning daily execution into the long-term intelligence behind better decisions.
Judi unlocks the value of your existing data by connecting systems like EDC, CTMS and ePRO to orchestrate the complex workflows they weren’t built to manage. Where other systems capture data, Judi connects data to people, actions and decisions. Judi is a value multiplier that turns fragmented data capture into real-time coordination. You’ve invested heavily in data capture. Now, make it perform.
Judi is the clinical trial optimization platform built for the AI era. It is where the work of your trial gets done, faster and better, across sponsors, CROs, AROs, core labs and sites. Every action is permissioned and recorded against the person, system or AI application that took it, so the AI you deploy runs inside the same controls as everything else. From study startup to database lock, every workflow in your trial runs in Judi, configured to your protocol, with every action, decision and handoff captured as the work happens in one audit-ready system.
Judi does the work an EDC or CTMS was never built to do. Those systems capture and store trial data. Judi coordinates the people, handoffs and decisions that move the trial forward across organizations.
Judi does not replace them, it works with them; essential data comes in from systems like EDC, CTMS and ePRO, and Judi orchestrates the cross-organizational workflows around it. That is why sponsors and CROs run Judi alongside the platforms they already own rather than in place of them.
Judi can run any workflow your trial needs. As of fall 2026, these are in production: user qualification, IRB submission, screening coordination, document development, eligibility, imaging, DSMB, 24/7 medical monitoring, clinical safety, remote source data verification, protocol deviations, adjudication and steering committee. More are being configured as clients bring them. Each workflow is configured to your protocol and operational plan rather than fitted to a template, which is why a workflow that is not on this list can still be built.
Judi is used by sponsors, CROs, AROs and core labs. More than 900 clients run trials on Judi, supporting 2,500+ trials in 120+ countries and 70,000+ sites, including 350+ Phase III studies across 20+ therapeutic areas. Sponsors use Judi for trial-wide oversight of work delegated across partners. CROs and AROs use it to deliver more trials without adding headcount. Core labs use it to receive complete, analyzable images. Organizations building their own AI capabilities for clinical trials use Judi as the governed environment those models run inside.
Judi uses AI in two ways. Native AI-assisted capabilities are built into the platform, starting with AI-assisted PHI redaction. Client AI models can also be embedded in Judi and run under the same controls.
Every AI action in Judi is governed the way a person’s is. AI is assigned to specific steps, given explicit permissions, held to review and approval gates where a human signs off, and written into the same audit trail as every other action. A person makes the call.
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.