Colombia INVIMA Medical Device Registration: Technical Files, CFS, and Apostille Requirements

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Colombia INVIMA Medical Device Registration: Technical Files, CFS, and Apostille Requirements

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This episode provides a detailed guide on the essential documents required for medical device registration in Colombia through the regulatory body, INVIMA. We cover the critical importance of the Certificate of Free Sale (CFS), the specific requirements for legalization and apostilles, the necessity of a local legal representative, and the comprehensive components of the technical file, including the mandatory Spanish language requirement. - What is the role of INVIMA in Colombia's medical device approval process? - Why is a Certificate of Free Sale (CFS) a mandatory document for registration? - What is an apostille, and when is it required for your submission documents? - Do foreign manufacturers need a local representative in Colombia? - What key information must be included in the technical file for INVIMA? - Is it possible to submit documents in English, or is Spanish mandatory? - What are the requirements for device labeling and Instructions for Use (IFU)? - How long is a medical device registration valid in Colombia? Pure Global offers expert regulatory consulting to streamline your MedTech or IVD company's entry into complex markets like Colombia. Our team acts as your local representative, leveraging in-country expertise and advanced AI tools to manage technical dossier submissions and ensure compliance with INVIMA's stringent requirements. We handle everything from regulatory strategy to post-market surveillance, allowing you to access over 30 global markets with a single, efficient process. Contact us at info@pureglobal.com, visit our website at https://pureglobal.com, or explore our free AI tools and database at https://pureglobal.ai to accelerate your global expansion.

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