DDR has extensive experience in contributing to the development of Medical Devices (MD), In Vitro Diagnostics and Combination Products.
Our deep understanding of the Medical Device and In Vitro Diagnostics 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 a Medical Device 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 Medical Device, to successfully attain certification and implement the correct maintenance processes; while ensuring compliance with Regulation requirements.