Whitepaper
Medical Devices

A Roadmap for SMEs and Startups

Key Steps Towards EU Regulatory Compliance for Medical Devices and In Vitro Diagnostic Medical Devices Manufacturers.

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Achieving compliance and market access

This whitepaper outlines key steps to navigate the conformity assessment, main challenges and regulatory expectations at every stage of your journey.

How approaching a NB earlier in the conformity journey can impact your regulatory strategy.
How to overcome most common challenges to achieve EU regulatory compliance.
Align regulatory requirements for each stage of your device lifecycle.
Organizations and guidance supporting SMEs and Startups in early stages.

TT&Truyền thông

Learn from global experts in healthcare standards

TT&Truyền thông

BSI

Sắp đến ngày 26/9/2024 – Hạn chót theo quy định (EU) 2023/607

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BSI

Sắp đến ngày 26/5/2024 – hạn chót theo quy định (EU) 2023/607

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