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Non-EU medical device manufacturers, importers, and distributors face the challenge of navigating the new, stricter EU MDR/IVDR regulations. MDIS from MedQAIR streamlines the process by centralizing documentation, automating submissions, and facilitating seamless communication with EU partners. Schedule a Free Demo!

Managing UDIs across multiple markets can be complex and prone to errors. MDIS from MedQAIR centralizes your UDI data, ensuring accuracy, easy tracking, and seamless regulatory submissions. Stay compliant with minimal effort and reduce the risk of mistakes. Schedule a Free Demo!

In post-market incidents, having up-to-date documentation accessible to all partners is crucial. MedQAIR’s MDIS platform ensures Legal Manufacturers' documentation is always available and simplifies vigilance reporting to databases like EUDAMED.

Managing EUDAMED docs, UDI updates, and Authorised Representatives is challenging enough. Add the back-and-forth of tracking documents through endless emails, and productivity takes a severe hit. MedQAIR’s MDIS centralizes communication, file transfers, and EUDAMED submissions in one secure platform. Schedule a free demo to see it in action.

Global medical device manufacturers face complex EU requirements: UDI, Authorised Representatives, and EUDAMED documentation. MedQAIR’s MDIS platform simplifies compliance by centralizing your files, automating EUDAMED submissions, and connecting you with EU partners. See how MDIS streamlines your EU compliance. Book a Free Demo!

Your EU Authorised Representative, fully digital. Upload Basic UDI-DIs and UDI-DIs in a few clicks, get fast reviews and release products onto the European market without the email chasing. Serving the EU, UK and Switzerland. Book a 30-minute demo with a MedQAIR regulatory expert below.