Clinical Trials

Increasing the effectiveness of R&D

Accelerate time to market, strengthen compliance and identify complications quicker. Gather empirical clinical evidence, measure adverse events and record personalised insights where symptoms matter most – in the real world.

  • Real-time, clinically approved patient monitoring
  • Symptom reporting – Phase 1 to Post-Market
  • Automatic data capture through the use of connected wearables – vital signs, movement, cognition
  • Questionnaires for large scale insights
  • Rapid, cost-effective deployment when starting a new trial
  • Auditable, regulatory complaint consent gathering