The bigger picture
Looking at Mili, its protagonists, and the flow of data.
Through several frontends, the Mili technology platform facilitates the collecting of voice data from participants in clinical studies and trials. It integrates existing speech biomarkers as well as machine learning models which can be automatically deployed on the collected speech data. Mili’s web-based interface allows study teams, sponsors and clinicians to plan, manage, and monitor studies.
Mili App
Patients undertake the assessment at home using the Mili app on their mobile devices.
ki:elements
speech biomarkers
Hosted by Mili to be
plugged-in to Mili
studies.
Mili Kokpit
Study team, sponsors and clinicians plan their studies or check the status of an ongoing study on the web-based platform.
Mili's frontends
Meeting patients where they are
Mili Phone
Mili phone is a patient-facing frontend that does not require any setup or installation from the participant. It is no device, no app, no tool – it’s a simple phone call.
Mili will reach out to study participants by calling them & guiding them fully automatically through a phone call while collecting their speech.
Listen to an example phone call for a MCI screening in a fully integrated setting (Mili integrated into study registration frontend) by clicking on the video.
Mili App
Mili App is the App frontend that can be used in in-clinic settings or by patients on their own mobile devices at home. It is design with participants in mind keeping it as intuitive and easy to use as possible.
View an example Mili App assessment for a MCI screening and get an idea about the app.
Integrating validated speech biomarkers
Plug & play speech biomarkers into your study
Validated speech biomarkers and predictive models can be integrated into Mili to enable a number of different use cases in one single platform, e.g. to (pre-)screen for MCI or to measure cognition with biomarker as an endpoint.
Compliance & data security
Ensuring secure handling of all data
Mili and all integrated ki:elements components are developed under our internal quality management system, following strict guidelines and principles, such as GDPR, ISO 13485:2016, FDA 21 CFR part 11 & part 820.70 and computer system validation (CSV).
Mili is fit for purpose to be used in highly regulated environments, like clinical drug trials.