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ITR proudly welcomed representatives from Nordic Semiconductor and Avnet Asia for a courtesy visit, marking a milestone in collaborative innovation for low-power, medical-grade, and miniaturized wearable products.

Achieving sub-10µA sleep mode current is a crucial engineering challenge that demands a combination of hardware, firmware, and power management optimizations.

Many startups and even established companies recognize that partnering with an Independent Design House (IDH) can accelerate product development, reduce risks, and ensure regulatory compliance. However, not all companies are ready to engage with an IDH.

Effortless UI Testing with AI: How Applitools is Transforming Visual Validation

When engaging with an Independent Design House (IDH) for medical device development, companies must prepare a set of essential documents, materials, and resources to ensure a smooth collaboration.

The success of a device depends on how well it integrates into existing clinical workflows and meets the practical needs of healthcare providers and patients.

Our approach is designed to mitigate risk, enhance collaboration, and accelerate time-to-market while maintaining strict compliance with medical regulations like ISO 13485, IEC 60601, and FDA guidelines.

Industry leaders in medical devices—whether large OEMs or established MedTech firms—expect Independent Design Houses (IDHs) to meet high standards in engineering expertise, regulatory compliance, risk management, and operational reliability. These companies are not just looking for a vendor but a long-term, strategic partner who can help bring innovative, market-ready devices to life efficiently and compliantly.

A Design for Cost (DfC) approach ensures that a product meets performance, safety, and compliance standards while remaining cost-effective from development to mass production.