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Electronic Development

Global Experts in Electronic Development

With huge experience working with ISO 13485 Quality Management Systems, and a track record of successfully manufacturing dozens of FDA-registered and CE-marked medical devices, we ensure the compliance of your products to international standards (IEC62304, ISO 14971, 93/42/EEC, and IEC 60601.
Our team helps you in the whole product development process or in independent stages of your product.
  • Requirements specification (User, cost and sector requirements)
  • Hardware components development
  • Verification and Validation (V&V plan development, systems integration tests, regulatory testing, static and dynamic unit testing, etc.)
  • Prototyping​
  • Maintenance (Updating Hardware, Obsolescence management, FW and verification test adaptation)​

We provide the following electronic development services

analog and digital circuit

Analog and digital Circuit diagram creation

layout

Layout (from two-level to multilayer electronic devices)

emc compliant

Complete EMC-compliant design

In-circuit tests

conformity

Conformity (CE, UL, ROHS)

Prototype electronic devices

recognition of vulnerabilities

Inspector software

technical analysis

Technical assessment of existing hardware to identify potential improvements

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