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