Clinical research-use and monitoring boundary statement
The operating boundaries that keep PatientTwin Bio clinically responsible and scientifically accurate.
Current authorised use
PatientTwin Bio supports clinical research operations, patient and participant digital twins, physiological studies, digital endpoint exploration, hospital-led remote monitoring and evidence review under authorised clinical and research governance.
Capabilities outside the platform boundary
- Autonomous diagnosis, prescribing or clinical decision-making
- Replacement of professional judgement or emergency-care systems
- Unapproved treatment recommendations
- Clinical claims without protocol, evidence and regulatory support
- Use of public illustrative data as real patient information
Clinical oversight
Alerts, derived indicators and digital-twin findings require review by authorised clinical or research teams. PatientTwin Bio organises evidence and workflow; it does not independently deliver care.
Near-space research accuracy
Stratospheric studies are treated as near-space physiology and environmental qualification under approximately terrestrial gravity. They are not represented as sustained microgravity studies.
Version: patienttwin-research-use-2026-07
Last updated: July 2026