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Regulatory Affairs solutions in Colombia for medical devices and IVDs
We can help you with any step of your regulatory strategy.
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Veraque Consulting is a regulatory affairs consultancy supporting medical device and in vitro diagnostic (IVD) manufacturers seeking market access in Colombia. We assist international companies throughout the INVIMA regulatory process, from product classification and regulatory strategy to dossier preparation, submission support, Sanitary Registration Holding services, and post-approval regulatory maintenance.
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Regulatory Affairs in Colombia guide
Let’s talk about regulatory affairs in Colombia. Check our comments and hints to have a better picture of this process.

Classification and Grouping guide
First things first. Classify your medical devices and decide how to group them is not an easy task. Read more about the latest rules and concepts you should keep in mind for this endeavor.