Staged consulting
Consulting fees agreed by stage, with a defined scope, deliverables and decision points for each phase.
For consumer electronics & wearable companies
AI and a clinically proven algorithm, for sensing technology toward medical use.
Your hardware already senses. We assess whether our proprietary database and clinically proven algorithm fit your signal and intended use, then plan integration, validation and clinical evidence with your team. AI-assisted analysis can support defined tasks under specialist review. We provide support toward medical and clinical status and approval, with clinical studies conducted by clinical partners.
Stage 01
Medical readiness assessment
When
You have a sensor, wearable or consumer device and want to know whether it can support a medical or clinical use.
Outputs
- Fit against our database and algorithm
- candidate medical use cases and claims
- gap map across hardware, data, software and evidence
- target markets and pathway options
- go / no-go recommendation
Stage 02
Algorithm integration and validation
When
Your sensing hardware is compatible with our technology and needs integration and performance evaluation for its intended medical use.
Outputs
- Data collection protocol
- licensed algorithm integration or an agreed co-development scope
- bench and analytical validation plan
- product-specific performance targets
- technical documentation to support the target-market pathway
Stage 03
Clinical validation and evidence
When
The product needs clinical evidence and a regulatory route in one or more markets.
Outputs
- Expert-led clinical evidence plan and study design support
- clinical partners to conduct clinical studies
- hospital and key opinion leader engagement
- publication strategy
- target-market pathway and submission planning with specialist partners
Stage 04
Medical launch and scale
When
The product is moving toward medical and clinical channels.
Outputs
- Medical go-to-market plan
- channel and partner options
- pricing and reimbursement assumptions
- post-market data and surveillance plan
- lifecycle and next-indication roadmap
Engagement models
Three ways to work with us
Algorithm licence
License our clinically proven algorithm for an agreed product, intended use and markets, with integration and validation responsibilities defined in the terms.
Co-development
Develop a product with us under an agreed scope, with profit share, IP ownership and decision rights defined before work begins.
Clinical-grade describes a product-specific performance goal, not a status conferred by Vie Nova. Evidence and validation must support each intended use; regulatory decisions rest with the relevant authority.
Terms are agreed before work begins: scope, stages and fees; licence field of use and territory; background and new IP; data responsibilities; confidentiality; and, for co-development, the profit-share basis and decision rights. Models can be combined, for example a staged assessment that leads to a licence or co-development.
Contact
Discuss your product
[email protected]
Singapore · China · Australia