With You at Every Step of Your Compliance Journey

Nemedio’s team of Regulatory and Quality experts offers a wide range of services to support you at every step of the device development process.

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Regulatory Analysis & Strategic Planning

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Clinical Testing

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Risk Management

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Software Design & engineering

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Usability & Human Factors

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IEC 60601 Adherence & Collaterals

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Design to Manufacturer Transfer

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Training Curriculum Development

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Post-Market Surveillance

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FDA Q-Submission Meeting Preparation

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Design & Development Planning

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Quality Team Vetting & Placement

Let's Work Together

We want to help bring your mission-critical device to market. Get in touch to learn more.