Judi orchestrates workflows across sponsors, CROs, AROs, core labs and sites in one governed environment, closing the operational gaps that stall clinical trials. By reducing manual effort and eliminating fragmented handoffs, teams optimize performance, cut friction and pick up speed. Trials deliver on time, with quality results, built-in compliance and continual audit readiness.
Ultimate accountability rests on your shoulders, to your board, regulators and patients. But bringing a therapy or device to market requires managing an extensive network of partners and outside vendors, and you remain responsible for the trial execution even when the work is delegated. Without centralized visibility, every cross-organizational handoff introduces operational risk. Judi eliminates blind spots by unifying your entire trial ecosystem under one governed workflow layer:
Growth is the goal and the problem. Your team is resource-constrained, tasked with doing more under tighter budgets. Every new trial adds another set of systems, logins and SOPs to juggle. The more you win, the harder it gets to deliver.
Judi allows you to scale operations successfully. Automations and AI-assisted tools build efficiency into the work, and every workflow for every trial runs on one unified platform. Your teams gain consistency and structure, and your sponsors see the work without having to ask. That is how you delight your clients and win more business.
Your independent reviewers should be assessing images, not waiting on them. Too much of what arrives is incomplete, mislabeled, late or not analyzable. Fixing it falls back on the study team, so images stall, then land on your reviewers all at once and there is yet another review crunch before a major milestone.
Judi helps the study team do real-time, high-quality image processing. Identifiers are stripped from DICOM tags and masked in the pixels, while automatic quality checks flag findings so they get actioned before delivery. Your reviewers open complete, analyzable images and get to work straightaway.
Judi is a clinical trial optimization platform for every organization involved in a clinical trial. That includes sponsors across pharma, biotech and medical device, plus CROs, AROs, sites, imaging core labs and other vendors. Judi brings the handoffs between them into one governed workflow, so work keeps moving and every decision stays traceable.
Yes, Judi works for trial sponsors, CROs and AROs. Some sponsors outsource operational work to CROs and AROs, and with view access, they use Judi to oversee the whole trial and keep every action and decision provable. Others use Judi directly to perform operational work in-house.
CROs and AROs use Judi to deliver trials across many sponsors from one platform, so each new trial adds capacity, consistency and scalability instead of complexity and cost.
Yes. Judi supports medical device trials. That includes capturing device attributes against each patient and timepoint, adjusting the workflow when the device or trial changes mid-study and offering right-sized, affordable solutions to fit trial size.
Judi collects images, automatically de-identifies them on two levels (within DICOM tags and pixels) and automatically performs QC to confirm modality and data acquisition compliance. Judi then automatically transfers the images to the core lab. Every step Judi handles is captured on a verifiable audit trail.
Core lab reviewers receive complete and analyzable images and can get to work without delay.
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.
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.
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, and 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.
Regulators ask the same questions of AI that they ask of people: who authorized the action, whether that authorization was in place at the time, and where the decision trail is afterward. Judi answers all three.