• Comprehensive Understanding: Gain insights into the technical documentation requirements of the In Vitro Medical Device Regulation (IVDR) EU 2017/746, covering the entire product life cycle.

  • Key Learning Objectives: Learn to differentiate between IVDD and IVDR in technical documentation. Understand the essential elements of technical documentation, including its structure, critical areas, and reports necessary for compliance.

  • Notified Body Assessment: Familiarize yourself with how notified bodies evaluate technical documentation, ensuring you are prepared for assessments.

  • Interactive Training: Prepare to create live documents that align with IVDR requirements. Understand the nuances of critical areas and the significance of up-to-date, comprehensive documentation.

Elevate your understanding of IVDR requirements and enhance your technical documentation skills. Fill in the form to excel in IVDR compliance.

IVDR Technical Documentation Training Course 

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