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𝗬𝗼𝘂𝗿 𝘁𝗿𝘂𝘀𝘁𝗲𝗱 𝗘𝗨 𝗟𝗲𝗴𝗮𝗹 𝗠𝗮𝗻𝘂𝗳𝗮𝗰𝘁𝘂𝗿𝗲𝗿 𝗳𝗼𝗿 𝗠𝗲𝗱𝗶𝗰𝗮𝗹 𝗗𝗲𝘃𝗶𝗰𝗲𝘀 Outsource regulatory responsibility and fast-track your devices to the European market with CE-Med – ISO 13485 certified, MDR-compliant, and ready to scale with you. 𝗢𝗻𝗲-𝗦𝘁𝗼𝗽 𝗦𝗼𝗹𝘂𝘁𝗶𝗼𝗻: Complete services or modular support - Flexibly tailored to your needs. 𝗣𝗲𝗿𝘀𝗼𝗻𝗮𝗹 & 𝗖𝗼𝗻𝗻𝗲𝗰𝘁𝗲𝗱: Your dedicated contact backed by 100+ experts. 𝗙𝗮𝘀𝘁𝗲𝗿 𝗠𝗮𝗿𝗸𝗲𝘁 𝗔𝗰𝗰𝗲𝘀𝘀: With ISO 13485 certification & full-scope notified body support. 𝗟𝗶𝗳𝗲𝗰𝘆𝗰𝗹𝗲 𝗣𝗮𝗿𝘁𝗻𝗲𝗿𝘀𝗵𝗶𝗽: From market entry to long-term success - reliable and sustainable. 𝗪𝗵𝗼 𝗶𝘀 𝘁𝗵𝗶𝘀 𝗿𝗲𝗹𝗲𝘃𝗮𝗻𝘁 𝗳𝗼𝗿? 🔹 International manufacturers without an EU entity seeking fast market access 🔹 Companies within the EU looking to outsource regulatory responsibilities 🔹 Start-ups focusing on product development Contact us at any time – we will find a pragmatic solution for your needs. 📞 +49 451 808 503 60 📧 info@qtec-group.com

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