Costa Rica

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Regulatory Affairs solutions in Costa Rica 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 Costa Rica. We assist international companies throughout the Ministry of Health regulatory process, from product classification and regulatory strategy to dossier preparation, submission support, Costa Rica Registration Holder (CRH) services, and post-approval regulatory maintenance.

Our top articles

Articles

Costa Rica Holding services guide

A Holder plays an important role as your legal representative. Learn about its key roles and responsibilities to get the best from this partnership.

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.

Regulatory Affairs in Costa Rica guide

Let’s talk about regulatory affairs in Costa Rica. Check our comments and hints to have a better picture of this process.

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