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Webinar Gallery

RAQA Deep Dives #6: Adverse Events: Learning from Others' Mistakes with Karolina Nożewska

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Empower yourself to transform adverse events into valuable lessons with our upcoming RAQA Deep Dives session led by expert Karolina Nożewska. Click Here to Register

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. Click here for all resources

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. Click here for all resources

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. Click here for all resources

RAQA Deep Dives #2: Collaboration is Key: Leveraging Teamwork for Surveillance with Tobias Winstel

Learn how teamwork enhances literature searches and safety surveillance with Tobias Winstel in this RAQA Deep Dives session. Click here for all resources.

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. Click here for all resources

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. Click here for all resources

Tough Questions by MedTech Leading Voice: Featuring an Expert Panel

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. Click here for all resources

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