Dive into the intricate world of regulatory classifications with Veronika Valdova as she shares real-world examples of medical devices that challenge traditional classification boundaries, creating regulatory conundrums across global markets.
On Thursday's Webinar 'Drug in the US, device in the EU: Navigating the Treacherous Waters of Combined Registrations,' we will step into the shoes of an RAQA professional grappling with products that intersect the drug-device domains in varying regions and discover the obstacles and nuances faced in this complex regulatory arena.
🎙️ Speaker: Veronika Valdova
📌 Where: Zoom Webinar
🗓️ When: May 2, 4pm CET / 11am EST
⏱️ Duration: 30 minutes
📚 Theme: Drug in the US, device in the EU: Navigating the Treacherous Waters of Combined Registrations
Gain expert insights from Veronika Valdova on strategies for navigating classification challenges and discover the key considerations essential for RAQA professionals dealing with dual-classified products. Delve into compelling case studies where Veronika Valdova has successfully guided companies through drug-device classification hurdles.
Join us for a captivating RAQA Deep Dive Session with Veronika Valdova as we delve into the intricate world of regulatory classifications for medical devices straddling the drug-device line across diverse regions. In this upcoming webinar, titled "Drug in the US, device in the EU: Navigating Combined Registrations," we will journey through the challenges and solutions in this dynamic landscape.
Don't miss out on this Webinar! Register here to access the live event, recordings, and valuable resources.
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