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Clinical trials
Working with clinical trials?
Mevia’s implementation method is simple, straightforward and is easily customised to your existing process.
Before study
Adaption to protocol
Mevias solutions are customised according to protocol, what data is needed and to best support the participants and investigators.
Integration of package solution
Mevia's packages solution are adapted and integrated to your existing package designs and sent for production at your selected Clinical manufacturing organisation (CMO).
Distribution of package solutions
The devices are sent direct to the sites or your CMO that provides starter kit of the package solutions to participants.
During study
Introduction to patient
Mevia sends out an SMS with instructions to participants after getting a trigger through the Interactive Web Response System (IWRS) or Mevia’s dashboard.
Follow real-time data
The data is sent to Mevia’s dashboard where it can be accessed from different administrations roles to make sure the right data is accessed by the right person.
Maintenance of devices
The devices are monitored and updated through Mevia’s system to make sure they work well and are used correctly.
After study
Collection of devices
The devices are collected by the sites and either reused or sent back to Mevia for reuse or proper recycling.
Safe data transfer
The data gets sent to the sites and stored in your choice of IWRS.
Research validation
The data enables high statistical power with a smaller patient sample size, makes it easier to set dose regimen and show competitive advantages.
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