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Qmedify

Qmedify | Simplifying EU Medical Device Certification Qmedify is a digital platform built to streamline the complex process of getting medical devices certified under the EU Medical Device Regulation (MDR). Instant device classification – Identify your device’s MDR class for free, in minutes. Tailored certification pathways – Step-by-step guidance based on your device class. Expert-backed tools – Access templates, documentation, and checklists designed by regulatory experts. Faster time to market – Cut down the cost, confusion, and time it takes to get certified. Whether you’re a startup innovating in medtech, a growing company entering the EU market, or a regulatory pro looking for a smarter tool — Qmedify is built to support your journey.#MedTech #MDR #EUregulations #MedicalDevice #DigitalHealth #Startups #HealthTech

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HeadquartersRiga, LatviaEmployees2(1 to 10)LinkedIn profileLinkedIn

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