qtec CE-Med
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đŹđźđđż đđżđđđđ˛đą đđ¨ đđ˛đ´đŽđš đ đŽđťđđłđŽđ°đđđżđ˛đż đłđźđż đ đ˛đąđśđ°đŽđš đđ˛đđśđ°đ˛đ Outsource regulatory responsibility and fast-track your devices to the European market with CE-Med â ISO 13485 certified, MDR-compliant, and ready to scale with you. đ˘đťđ˛-đŚđđźđ˝ đŚđźđšđđđśđźđť: Complete services or modular support - Flexibly tailored to your needs. đŁđ˛đżđđźđťđŽđš & đđźđťđťđ˛đ°đđ˛đą: Your dedicated contact backed by 100+ experts. đđŽđđđ˛đż đ đŽđżđ¸đ˛đ đđ°đ°đ˛đđ: With ISO 13485 certification & full-scope notified body support. đđśđłđ˛đ°đđ°đšđ˛ đŁđŽđżđđťđ˛đżđđľđśđ˝: From market entry to long-term success - reliable and sustainable. đŞđľđź đśđ đđľđśđ đżđ˛đšđ˛đđŽđťđ đłđźđż? đš International manufacturers without an EU entity seeking fast market access đš Companies within the EU looking to outsource regulatory responsibilities đš Start-ups focusing on product development Contact us at any time â we will find a pragmatic solution for your needs. đ +49 451 808 503 60 đ§ [email protected]
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