Medical Devices and In Vitro Diagnostics

DDR has extensive experience in contributing to the development of Medical Devices (MD), In Vitro Diagnostics (IVD), Companion Diagnostics and Combination Products.
Our deep understanding of the MD and IVD Regulations enable us to provide customized recommendations for optimal product development to successfully obtain the CE mark. DDR also contributes to the elaboration of the documents needed to support the certification.


DDR’s strategic services positively contribute to the success of devices development, avoiding common pitfalls and identifying fast and cost-effective ways to successfully certify your device.


DDR offers high-quality operational services, which are essential for the development of your devices, to successfully attain certification and implement the correct maintenance processes, while ensuring compliance with Regulation requirements.

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