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Current Health Trial Pharmacovigilance and Real-World Evidence

by Current Health

Applies configurable study and safety pathways, supports continuous pharmacovigilance.

Current Health
Industry
HealthcareRemote Patient Monitoring
Use cases
Condition MonitoringRegulatory ReportingQuality Compliance
Deployment
Public SaaSEdge/Local
Services
InstallationManaged ServiceSystem IntegrationSupport & MaintenanceData AnalyticsSoftware Platform
Available in
United StatesUnited Kingdom
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The challenge

What operators are up against

Operators responsible for clinical-trial and commercial-therapy patients, investigational and approved therapies, wearable and connected devices, adverse events, symptoms, protocols, sites, sponsors, safety teams, and evidence programs cannot continuously inspect every operating condition or developing fault. Periodic checks leave gaps between readings, while isolated local indicators provide limited history and context. A late response can cause downtime, safety exposure, equipment damage, or incomplete compliance evidence. Teams need timely measurements, clear exceptions, and a defined operating response.

The solution

How Current Health Trial Pharmacovigilance and Real-World Evidence addresses it

Current Health Trial Pharmacovigilance and Real-World Evidence combines connected field data with application software. Connected devices and patient applications capture vital signs, symptoms, adherence, adverse-event, treatment, protocol, communication, and supported clinical or real-world records. The platform applies configurable study and safety pathways, supports continuous pharmacovigilance, detects deterioration. Sponsors and sites monitor safety, contact participants, escalate adverse events, support decentralized visits, adapt programs, prepare analyses.

How it works

Teams configure the monitored assets, users, and operating rules. Connected devices and patient applications capture vital signs, symptoms, adherence, adverse-event, treatment, protocol, communication, and supported clinical or real-world records. Current Health wearable and connected devices send measurements through the supplied tablet or supported home path to the clinical platform and integrated EHR. The platform applies configurable study and safety pathways, supports continuous pharmacovigilance, detects deterioration. Sponsors and sites monitor safety, contact participants, escalate adverse events, support decentralized visits, adapt programs, prepare analyses.

SenseConnected devices and patient applications capture vital signs, symptoms, adherence, adverse-event, treatment, protocol, communication, and supported clinical or real-world records.
ConnectCurrent Health wearable and connected devices send measurements through the supplied tablet or supported home path to the clinical platform and integrated EHR.
AnalyzeThe platform applies configurable study and safety pathways, supports continuous pharmacovigilance, detects deterioration.
ActSponsors and sites monitor safety, contact participants, escalate adverse events, support decentralized visits, adapt programs, prepare analyses.

Vendor documentation: vendor website

Evidence level: L1 · Vendor-stated: how evidence levels work

Uses this hardware

REQUIREDCurrent Health FDA-Cleared Wearable

Current Health FDA-Cleared Wearable

Current Health
Current Health Wearable
SensorBluetooth
REQUIREDCurrent Health Home Hub

Current Health Home Hub

Current Health
Home Hub
GatewayCellular
RECOMMENDEDCurrent Health Axillary Temperature Patch

Current Health Axillary Temperature Patch

Current Health
Axillary Temperature Patch
SensorBluetooth

Why teams choose it

Field data capture

Connected devices and patient applications capture vital signs, symptoms, adherence, adverse-event, treatment, protocol, communication, and supported clinical or real-world records

Bluetooth connectivity

Current Health wearable and connected devices send measurements through the supplied tablet or supported home path to the clinical platform and integrated EHR

Operational analytics

The platform applies configurable study and safety pathways, supports continuous pharmacovigilance, detects deterioration

Operational response

Sponsors and sites monitor safety, contact participants, escalate adverse events, support decentralized visits, adapt programs, prepare analyses

Deployment context

Designed for pharmaceutical and biotechnology sponsors, clinical-development teams, research sites, pharmacovigilance groups, medical affairs, providers, patients, and Phase I-IV evidence programs

Role-based visibility

Authorized users can review current status, history, and operating exceptions

What’s different

Attributes fewer than 20% of comparable Healthcare listings share:

Regulatory Reporting

Prerequisites

Limitations / not covered

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