MEDICAL DEVICES


Medical Devices regulation is a modern law capable of modifications and upgrades.


The procedures for obtaining the CE mark change, also, according to the directive apply.

For all this, everyday is becoming more important to perform studies with medical devices, both for obtaining the CE mark as to monitor the safety of such products.

MEDITRIAL offers the opportunity to manage this study, following the law and contributing the most stringent quality standards.

Meditrial Medical Devices