Precision diagnostic monitoring, real-time and in real life
Advances at the medical frontier demand more capable electronics. Better bio‑electrical insight means earlier clinical decisions, safer care and stronger evidence.
Our medical skin patches provide reliable interfaces for ExG diagnostic monitoring, including ECG, EEG, EMG, EOG and GSR applications. Electrode layouts and placement are tuned to each application; adhesives and carriers match wear time and body zone; and packaging is validated to preserve performance throughout shelf life.
Monitoring applications
Monitoring applications place different demands on electrode design, materials and skin interaction. Signal amplitude, impedance stability, motion sensitivity and wear time vary significantly between cardiac, neurological and muscle monitoring use cases.
Quad designs and manufactures adhesive electrode patches tailored to each signal type — aligning electrode chemistry, geometry, adhesives and interconnects with your device architecture and intended use.
While ECG, EEG and EMG are the most common applications, the same technology platform supports a broader range of ExG measurements, including EOG (electrooculography), EDA/GSR (electrodermal activity) and other bio-potential sensing modalities.
What we build
For monitoring applications, patch architecture is driven by signal type, body zone and intended wear time. Quad’s ExG platform supports multiple electrode configurations and system architectures, allowing wearable patches to be tailored to the specific requirements of ExG monitoring systems, including ECG, EEG, EMG, EOG and GSR.
Prototype to volume
To get started, just share a sketch, a proposed stack, or your recorder specs. Together we select materials, design the printed electrodes, agree the connectivity strategy, and validate packaging and shelf life.
Designs are scaled to production with consistent quality and reliable lead times, supported by automated manufacturing and validated process control.
Skin lab and packaging
We evaluate material stacks on real skin, assess reliability and use accelerated ageing to align device performance with packaging and logistics requirements. Adhesive performance and removal comfort are validated under realistic use conditions.
Validated barrier pouches protect hydrogel performance during storage and handling.
Standards & Quality
Quality and regulatory compliance are embedded at every stage of Quad’s operations — from early material validation to automated high-volume production.
Quad operates under a certified ISO 13485 quality management system, ensuring full alignment with medical device regulatory requirements throughout development and manufacturing.
Our manufacturing facilities are FDA registered for medical device production. Processes, documentation and traceability are structured to support OEM partners supplying regulated markets in the US and globally.
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