Life After Certification: Thrive In The Era Of IVDR Compliance

This webinar focuses on establishing sustainable regulatory processes that support continued compliance throughout the product lifecycle.

Understand your ongoing obligations after IVDR certification

IVDR compliance goes beyond certification, requiring ongoing vigilance, post-market activities and effective change management.

Speakers

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Regulatory Lead Notified Body IVDR, BSI

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Senior Technical Specialist & Scheme Manager, BSI - AM Session

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Technical Specialist & Scheme Manager, BSI - PM Session

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Business Development Manager – IVD - AM Session

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Senior BDM - IVDR Lead, BSI - PM Session

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BDM, APAC China, BSI - AM Session

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Senior BDM, APAC Korea, BSI - AM Session

Connect directly with our experts and build your understanding of key regulatory requirements and the conformity journey.

Engaging a Notified Body under the In Vitro Diagnostic Medical Devices Regulation (IVDR) for the first time raises a lot of questions. This session explains the conformity assessment process step by step and the role of the Notified Body in your IVDR conformity assessment, giving you a greater understanding of where to start with your IVDR certification journey.

8 October 2026 - 09:00 BST or 16:00 BST

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Learn what Notified Bodies expect from IVDR technical documentation during an assessment; including how to align clinical evidence and quality management processes, and how to strengthen your documentation to avoid delays in your conformity assessment.

22 October 2026 - 09:00 BST or 16:00 BST

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Why Join This Series

Talk with our regulatory specialists and dedicated technical experts, who bring deep scientific knowledge of the industry.

An open fireside discussion and live Q&A in every session. Submit your questions when you register.

Understand regulatory requirements and the deficiencies most often raised during assessment, before they cost you time.

Certification is just the beginning. Prepare for ongoing compliance across the full product lifecycle.

Who Should Attend

Regulatory Affairs Managers And Specialists.

Regulatory Affairs Directors.

Quality And Regulatory Professionals.

SME Leadership, Including Managing Directors.