
mili platform
Configurable, validated,
built for scale
Mili is ki:elements’ end-to-end platform for running speech-based assessments in clinical trials. Designed to navigate the complexity of multi-site research.

mili platform
Configurable, validated,
built for scale
Mili is ki:elements’ end-to-end platform for running speech-based assessments in clinical trials. Designed to navigate the complexity of multi-site research.
mili platform
Configurable, validated,
built for scale
Mili is ki:elements’ end-to-end platform for running speech-based assessments in clinical trials. Designed to navigate the complexity of multi-site research.
No device logistics.
Maximum reach.
Participants complete assessments via telephone, smartphone, tablet, or browser — whatever they already have. No devices to ship, no setup burden.
Mili Phone
VOICE AGENT
Participants answer a voice agent guided call, sheduled for a time of their choice. Zero setup burden.
Mili App
smart Devices
Mili Web
Browser

No device logistics.
Maximum reach.
Participants complete assessments via telephone, smartphone, tablet, or browser — whatever they already have. No devices to ship, no setup burden.
Mili Phone
VOICE AGENT
Participants answer a voice agent guided call, sheduled for a time of their choice. Zero setup burden.
Mili App
smart Devices
Mili Web
Browser

No device logistics.
Maximum reach.
Participants complete assessments via telephone, smartphone, tablet, or browser — whatever they already have. No devices to ship, no setup burden.
Mili Phone
VOICE AGENT
Participants answer a voice agent guided call, sheduled for a time of their choice. Zero setup burden.

Mili App
smart Devices
Mili Web
Browser
One system, from protocol to output
One system, from protocol to output
One system, from protocol to output
Design protocols, manage sites, monitor participant progress, and trigger or schedule assessments through a single interface built for the demands of multi-center clinical trials.
Design protocols, manage sites, monitor participant progress, and trigger or schedule assessments through a single interface built for the demands of multi-center clinical trials.
Integrated analytics
Integrated analytics
Speech data feeds directly into ki:elements’ biomarker pipeline. Measures are returned automatically, without the need for a separate export or processing step.
Speech data feeds directly into ki:elements’ biomarker pipeline. Measures are returned automatically, without the need for a separate export or processing step.
Real-time and remote collection
Real-time and remote collection
Trigger in-clinic assessments on demand or schedule at-home sessions with automated notifications or phone calls. Your team stays in control of the cadence, whether participants are on-site or remote.
Trigger in-clinic assessments on demand or schedule at-home sessions with automated notifications or phone calls. Your team stays in control of the cadence, whether participants are on-site or remote.
Scales with your study
Scales with your study
From a 50-person pilot to a large Phase III study. Configurable workflows, role-based access, and multi-site architecture mean the platform grows with your protocol.
From a 50-person pilot to a large Phase III study. Configurable workflows, role-based access, and multi-site architecture mean the platform grows with your protocol.
Built for regulated environments
Built for regulated environments
Mili is developed and validated to operate in clinical trials. Every component is built under our internal quality management system and continuously maintained to meet evolving regulatory standards. Documentation can be provided for regulatory submissions.
Mili is developed and validated to operate in clinical trials. Every component is built under our internal quality management system and continuously maintained to meet evolving regulatory standards. Documentation can be provided for regulatory submissions.
✓ Developed under Computer System Validation (CSV)
✓ Compliant with FDA 21 CFR Part 11 & Part 820.70
✓ Follows Good Clinical Practice (GCP) guidelines
✓ Follows FAIR Principles for scientific data management
✓ GDPR compliant throughout
✓ Data hosted in ISO/IEC 27001, ISO 50001, ISO 22301 certified centres
✓ Developed under Computer System Validation (CSV)
✓ Compliant with FDA 21 CFR Part 11 & Part 820.70
✓ Follows Good Clinical Practice (GCP) guidelines
✓ Follows FAIR Principles for scientific data management
✓ GDPR compliant throughout
✓ Data hosted in ISO/IEC 27001, ISO 50001, ISO 22301 certified centres
© ki:elements GmbH 2026 · Saarbrücken, Germany
© ki:elements GmbH 2026 · Saarbrücken, Germany
© ki:elements GmbH 2026 · Saarbrücken, Germany

