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Upcoming webinars

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Building an Audit-Ready Justification Record

The justification record is one of the most scrutinised elements in technical documentation. Many teams struggle to articulate how each requirement is met, where the supporting evidence sits, and how this aligns with Annex II/III expectations. This session provides a structured, defensible approach to building a justification record that withstands auditor review.

Past webinars

AI Technology: For Regulatory Intelligence and Surveillance

Discover insights from our expert superpanel on AI's role in regulatory affairs. Gain knowledge on AI workflows, key concepts, policy implementation, and practical applications.

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RAQA Deep Dives #7: From Data to Insights: with Nicholas Wells

Join our RAQA Deep Dive session with Nicholas Wells to explore actionable insights and case studies on managing compliance challenges.

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RAQA Deep Dives #5: Catch Me If You Can: The Hide 'n Seek of Biocompatibility with Marina Daineko

Dive into the critical role of biocompatibility in medical device safety with expert Marina Daineko as she unpacks essential strategies and insights in our latest deep dive session.

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RAQA Deep Dives #4: AI and Smart Tools for Enhanced Surveillance​ with Veronika Valdova & Martin King  

Join us for a special edition webinar featuring experts Veronika Valdova and Martin King as they explore the latest advancements in AI automation and smart surveillance tools.

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RAQA Deep Dives #3: Drug in the US, device in the EU with Veronika Valdova

Discover the complexities of products classified as drugs in the US and devices in the EU with Veronika Valdova in this RAQA Deep Dives session.

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AI Technology: For Regulatory Intelligence and Surveillance

Learn how teamwork enhances literature searches and safety surveillance with Tobias Winstel in this RAQA Deep Dives session.

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RAQA Deep Dives #1: Demystifying the Regulatory Landscape with Martin King

Build a solid foundation in global regulatory landscapes and learn effective navigation strategies with Martin King in this RAQA Deep Dives session.

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EU MDR & IVDR Vigilance Expert Masterclass with Veronika Valdova

Master EU MDR & IVDR vigilance complexities with Veronika Valdova in this expert masterclass, covering post-market surveillance, submission processes, and compliance.

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Master EU MDR & IVDR vigilance complexities with Veronika Valdova

Get insights into regulatory obligations, risk management, and postmarket surveillance with our expert panelists on key topics for device companies in the EU and US. In this expert masterclass, covering post-market surveillance, submission processes, and compliance.

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Webinar Gallery

Explore our webinar gallery featuring expert-led discussions on MedTech and regulatory affairs — from AI-powered regulatory intelligence to deep dives into MDR/IVDR, vigilance, biocompatibility, and global compliance challenges.

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