
Our mission is to accelerate the development and market access of innovative medical technologies by providing high-quality clinical, regulatory and scientific support. We aim to make complex MedTech development and regulatory pathways clearer and more manageable, helping companies generate the evidence they need, meet regulatory requirements and ultimately bring safe and effective medical technologies to patients.
1 des employés de chez MDx CRO ont examiné MDx CRO dans diverses dimensions culturelles, en donnant leur avis sur des sujets allant des évaluations des dirigeants au rythme de travail. La dernière évaluation date d'il y a 15 journées.
MDx CRO is a MedTech contract research organization and regulatory consultancy supporting medical device, IVD, digital health and precision medicine companies across clinical research, regulatory affairs, quality, usability, SaMD, and market access. Based in Spain, Portugal, UK, and operating internationally, MDx CRO brings together experienced clinical research professionals, regulatory specialists and former notified body experts to help MedTech companies navigate complex regulatory requirements and bring safe, effective technologies to patients. Our expertise spans medical device clinical investigations, IVD analytical and clinical performance studies, companion diagnostics, MDR and IVDR compliance, technical documentation, software and AI-enabled medical devices, usability engineering and post-market activities. MDx CRO works with innovative companies worldwide, combining scientific and regulatory expertise with a collaborative, agile and practical approach.
It was natural easy going, the team was very supportive.

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