When reading the whitepaper, you will learn:

  • How MDR, CRA, and NIS2 affect medical technology suppliers directly and indirectly.
  • Why even non-medical components must meet strict regulatory requirements.
  • What documentation and technical information OEMs expect from their suppliers.
  • How cybersecurity regulations like the CRA change product development and support.
  • Why NIS2 shifts responsibility for security across the entire supply chain.
  • Why regulatory readiness strengthens your market position and customer relationships.

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