Costa Rica
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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.

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

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.

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