Webinar
Medical Devices

How to Use Risk Mapping to Set Up Your Project for Success

La gestione del rischio non è solo un requisito normativo: è una guida strategica per uno sviluppo dei dispositivi più intelligente ed efficiente

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Per startup e SME che si preparano a presentare domande MDR o IVDR.

Presentazione di approcci pratici alla mappatura dei rischi che siano in linea con le aspettative MDR e IVDR, restando al tempo stesso realistici per organizzazioni con risorse limitate.

Effective risk mapping can mean the difference between costly delays and a smooth path to market.
How to identify risks early, link them to design and development activities.
Use your risk map to guide smarter decisions throughout the product lifecycle.
How startups and small manufacturers can accelerate growth.
Prioritizing quality management and achieving device certification in the EU.

Register for our BSI Insight Series: Startup Edition Webinars

Join us for this webinar series tailored for regulatory, R&D, and quality professionals, as well as founders of startups and small manufacturers.

This webinar series is designed for regulatory, R&D, quality professionals, and founders of startups and small manufacturers.

Team members from larger manufacturers seeking a broader understanding of quality and EU regulatory requirements will also benefit from this series.

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This webinar will break down the essentials of MDR and IVDR classification rules and show you how to properly define indications for use in a way that aligns with regulatory expectations.

Through clear explanations and practical examples, you’ll gain confidence in navigating this complex but fundamental part of the conformity assessment process.

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This webinar will break down design controls and clinical planning into clear, actionable steps tailored for resource-limited organizations.

You’ll learn how to connect design activities with risk management, plan clinical evidence in line with regulatory expectations, and document your process effectively to support MDR and IVDR submissions.

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This webinar will introduce startups and small companies to the fundamentals of human factors and usability engineering in the context of MDR and IVDR compliance.

You’ll learn how to integrate usability considerations early in development, reduce use-related risks, and strengthen your technical documentation for regulatory submissions.

10 March 2026 - 16:00 GMT

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This webinar will provide clear guidance on evaluating manufacturing pathways, including insourcing versus outsourcing, supplier considerations, and how to align your production strategy with MDR/IVDR requirements.

You’ll learn how to make informed decisions that balance quality, cost, timelines, and regulatory obligations—helping you bridge the gap between early development and successful market launch.

14 April 2026 - 16:00 GMT

Register for the webinar

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