Preparing high-quality Performance Evaluation Reports (PER) and robust Post-Market Surveillance (PMS) documentation is essential for successful IVDR compliance, but getting it right the first time remains a common challenge. In this webinar, DNV’s IVDR experts will share practical best practices and highlight frequent pitfalls observed during assessments, helping you understand the various approaches to creating compliant documentation.

Join us to gain a clearer understanding of IVDR requirements and expectations, and learn how to effectively connect clinical evidence, performance evaluation, and post-market activities into a coherent, compliant framework. The session will provide actionable insights to support the development of documentation that is consistent, defensible, and aligned across the product lifecycle, enabling an overall smoother and more efficient conformity assessment process.