MDx IS YOUR CRO FOR MEDICAL DEVICES AND IVDS
At MDx, we pride ourselves on delivering expert support and guidance for your medical device and in-vitro diagnostic projects.
As a partner in the medical device and IVD innovation landscape, our services include regulatory consulting, clinical research, quality assurance, and a wide range of specialized support tailored to your unique needs.
Our goal is to help you navigate the complex process of bringing medical devices and IVDs to market while ensuring compliance with IVDR and MDR regulations. If you have any questions or would like to discuss how we can assist you, please contact us in the form below.
REQUEST YOUR EXPERT CONSULTATION
MDx offers a free initial consultation to better understand your project, medical device, software as a medical device, or IVD under IVDR and MDR regulations. Our team of experts is ready to help you navigate the regulatory, clinical research (including clinical trials, clinical investigations, and clinical performance studies), and quality strategic planning aspects of your project.
To request your expert consultation, complete the form with your name, email address, and a brief description of your project. We will review your information and reach out to discuss the next steps.
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We appreciate your interest in partnering with MDx for your medical device and IVD innovation needs. Our team looks forward to working with you to help your projects achieve success.
MED IVD HEALTHTECH S.L ha sido beneficiaria de la subvención de contratos de trabajo de la Comunidad de Madrid, cofinanciado por el Fondo Social Europeo dentro de la Ayuda a la Recuperación para la Cohesión y los Territorios de Europa (REACT-UE), a través del Programa Operativo Regional FSE, en el marco del Programa Impulso a la Contratación Estable de Jóvenes para la Recuperación Económica, gestionado por la Dirección General del Servicio Público de empleo de la Consejería de Economía, hacienda y empleo de la Comunidad de Madrid.
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