EvidentIQ AI Innovation
We meet your demands across clinical operations, clinical data management and patient centricity with a suite of applications designed and supported by industry veterans.
Coding concomitant medications against the WHODrug Global dictionary is demanding work. Across multi-site studies, the manual workload adds up fast. We are integrating WHODrug Koda, the AI coding engine from Uppsala Monitoring Centre, directly into our EDC so drug verbatims are matched to standardized codes automatically.
Koda reads raw drug names, route, and indication from site-entered data and returns the coded drug name and ATC code. No pre-formatting needed.
Every suggestion goes through a structured approval workflow. Coders accept, override, or reassign each result. Every decision is logged in a full 21 CFR Part 11 compliant audit trail.
Koda is trained and continuously maintained by UMC. Reliable autocoding performance from the start, without the build time or data volume a custom model requires.
Study build is where timelines slip, before a single patient is enrolled. We are developing an AI-assisted form builder for Dacima that reads protocol logic and generates structured, compliant eCRF forms ready to deploy. No configuration code required.
Configuration Code
Faster Study Startup
Protocol to eCRF time
Clinical data comes from sites, devices, patients, and partners. Our platforms connect your entire study ecosystem so data from wearables, patient communities, and recruitment networks lands in one validated, audit-ready environment. No manual reconciliation.
Biosensors, implanted devices, and remote monitoring tools connect directly to the EDC. Measurements enter the study database automatically, without transcription.
Carenity and Future4Patients connect recruitment, enrollment, and patient-reported outcomes directly to your trial environment. 1,200+ disease areas covered, compliantly.
Integrations with third-party EDC systems, FHIR sources, ERP tools, and open API access for custom environments.
Studies slow down when answers are hard to find. A coordinator unsure about a completion rule. A CRA chasing a protocol clarification. A new site team getting up to speed three weeks into screening.
We built tools to close that gap, putting study-specific knowledge within reach of every person on a trial, backed by our clinical experts when it matters.
Site staff and study teams can ask questions and get immediate answers grounded in the actual protocol, CRF guides, and training materials for their trial. Not generic responses. Answers specific to the workflow they are in.
Coordinators, CRAs, and data managers each get relevant onboarding, procedural guidance, and CRF walkthroughs built around their study from the start.
Our clinical and technical team is directly reachable when a question goes beyond what a tool can answer. No escalation chains. No support queues. A person who knows your trial.
