AI-ready data2025-10-07T13:29:52+00:00

Design Your Device
to Deliver AI-Ready Data

The success of AI applications depends on the data feeding the algorithms. More data isn’t always better—what matters is high-quality, clinically relevant signals collected efficiently and securely.

To accelerate time to market and reduce risk, tap into proven expertise for your AI data pipeline—so your team can focus on your algorithms and your competitive edge.

With our pre-certified biosensors, proven hardware and software building blocks, and milestone-based pricing, you can get to market faster, at lower risk, and with capital preserved for growth.

TAP INTO PROVEN EXPERTISE IN AI-READY DATA

Building the data pipeline that feeds your algorithms is a massive undertaking. From signal acquisition and power management to secure data transmission and compliant cloud storage, every piece of the pipeline demands specialized expertise, acquired over years of continuous iterations and optimization.

High-fidelity signals depend on selecting the right sensors, optimizing placement and calibration, and implementing proper signal conditioning hardware and software to minimize noise and drift.

Efficient devices rely on low-current analog hardware, optimized firmware, and event-based collection strategies, with smart sleep cycles to balance energy use and continuous performance.

Raw signals should be cleaned, filtered, and compressed at the edge, then refined through feature extraction and machine learning models to generate real-time clinical insights.

Robust pipelines follow ISO 13485, HIPAA, and FDA cybersecurity guidance, using encrypted transmission, controlled access, and lifecycle risk management to keep data secure.

FAQ

What are the requirements for making biosensor data AI-ready in low-power devices?2025-09-03T19:31:36+00:00

In low-power wearables and implants, AI-ready data must be clean, structured, and lightweight. Devices should preprocess signals to reduce noise and compress features before transmission. This minimizes power use while ensuring the data is usable for model training and real-time inference.

How do low-power constraints impact your medical device AI strategy?2025-09-03T19:31:56+00:00

Power limits may require preprocessing or signal classification to happen on-device, using lightweight models or thresholds. Full AI processing may be deferred to the cloud, so the device sends only essential features, reducing energy use while still enabling intelligent insights.

What are the tradeoffs between edge and cloud processing in low-power medical devices?2025-09-03T19:32:14+00:00

Cloud processing reduces on-device power use but increases wireless transmission needs, which can drain batteries quickly. Edge processing saves data transmission power by analyzing data locally, but requires more capable (and slightly more power-hungry) processors or more awake time. The decision where to process data is often driven by other factors as well, such as the likely frequency of updating the associated algorithms. The best approach often involves a balance of the two approaches, based on the specific application.

What are the tradeoffs between biosensor data quality and power usage?2025-09-03T19:32:33+00:00

Higher data quality often requires faster sampling, higher resolution, lower noise, and more frequent transmissions—all of which consume more power. To conserve energy, the first step is determining what the quality requirements truly are. The data must be good enough to enable the product to accomplish its current and future clinical goals, but superfluous quality only consumes power for no end benefit.

How do you optimize biosensor data collection for ultra-low power?2025-09-03T19:32:42+00:00

Optimization involves selecting the right sampling rate, minimizing sensor activation time, and balancing analog and signal processing to achieve the necessary signal quality—not the maximum possible signal quality. For wearable or implantable sensors, the goal is to capture meaningful data while keeping energy consumption minimal.

Result-based business model

Cash efficiency is a “do or die” proposition for any early stage company, and hourly-priced projects can quickly lead to cost and time overruns.

Our pricing is based on results, giving you the predictability you need to plan your budget and meet your funding milestones with confidence.

And with direct access to our project management system, you have real-time visibility into our progress so you always know where you are.

You pay for: Milestones completed

You don’t pay for: Our time

design for success

From napkin sketch to commercially-viable product, we take a holistic approach to product development, addressing all the required aspects for your device to be successful:

Technical
Ensuring the device can perform as required to deliver the intended clinical results

Usability
Ensuring the device can be operated in the intended clinical setting

Standards
Ensuring the design and development process is documented in compliance with ISO 13485:2016 and that the design meets the requirements imposed by relevant regulatory standards

Manufacturability
Ensuring manufacturing is feasible within your business case assumptions and identifying qualified suppliers and manufacturing partners

Financial
Optimizing device cost of goods sold (COGS)

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“In just one year, Nocturnal took our implantable cardiac monitor from a concept to a fully functional device.”
Jaeson Bang, Founder & CEO, Future Cardia

Our top team
is now
your team.

We are a small firm where everyone is an expert in their field, everyone is working hands-on with a client, and everyone is invested in your success.

Turn your sketch into reality.

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