OUTCOMES
- Optimize Patient/Site Experience
- Increase Diversity/Access to Clinical Trials
- Predictive Safety Monitoring
- Pharmacovigilance Paradigm Shift
- Improve Benefit/Risk Profile
- Optimize Path to Commercialization
- Accelerate Path to Effectiveness
Intrepid Partner Program
IntrepidTM
Partner Program
Accelerating the optimization of patient safety and health measurements in both clinical research and post market clinical care
INTREPID
PARTNER PROGRAM
Accelerating the optimization of patient safety and health measurements in both clinical research and post market clinical care
Bringing Continuous Patient Data to Contract Research Organizations, Academic Research Organizations, and other Technology Solution Companies
The IntrepidTM Partner Program enables the Life Sciences solutions ecosystem to deliver next generation near real time patient insights powered by high-fidelity medical grade biosensor data streams.
Digital Biomarkers
industry-leading portfolio of AI-based digital biomarkers
Regulatory Knowledge
Deep experience working with regulatory bodies
Technical Expertise
Proven ability to integrate advanced digital technologies into clinical operations
TECHNOLOGY
- SaMD Class 1 Platform
- 510K FDA Cleared dBMs
- dBM Development Pipeline
- Integration As A Core Design Principle
- Time Series Scalability & Performance
- Data Agnostic
- Unified Clinical Continuum
COMPANY
- Deep Industry Experience
- Data Science
- Digital Clinical Application
- Clinical Operations
- Regulatory Submission
- Clinical Continuum Execution
- Enterprise Sponsor Adoption
- 19 Global Patents Issued
- 20+ yrs of AI/ML Experience
True Real-World Data
Wearable biosensors can bring unprecedented insights to your clinical trial. With accelerateIQ, your organization can generate more data with greater patient insight, faster.
Decentralized Clinical Trials
Decentralized trials have the potential to expand patient pools and obtain more data to make better decisions. accelerateIQ unlocks this potential by providing continuous remote data collection which increases available information while reducing site visits.
Remote Monitoring
The physIQ platform makes monitoring patients in clinical trials an ongoing, continuous process whereby trial monitors can have access to near real-time data and reduce the need for face-to-face interactions.
Risk-Based Monitoring
Risk-based monitoring focuses activities to the evolving areas of greatest need which have the most potential to impact patient safety and data quality. With continuous data from accelerateIQ, you can uncover patient concerns and trial problems in near real time.
Patient Safety & Compliance
By collecting and analyzing physiological data and feeding that into a predictive analytics platform, accelerateIQ can help you anticipate safety concerns rather than react to them.
Study Setup and Initiation
Everything necessary to bring digital monitoring into your clinical trial
Study Design
Protocol Development
IRB Support
Logistics and Management
physiq handles all the logistics of your digital trial
Device Procurement and Provisioning
Kitting and Shipping
Inventory Management
Patient and Site Support
PHYSIQ PROVIDES ONGOING SUPPORT TO PATIENTS AND SITES
Site and patient training and ongoing support
Patient compliance monitoring
it's time to take action.
Contact physIQ Today.
