Bringing a medical device to market isn’t just about innovation—it’s about navigating a minefield of regulations, audits, and clinical risks. Whether you’re preparing for your first submission or managing post-marketing surveillance, there’s pressure to meet evolving global standards. You need a partner who can anticipate challenges, bridge knowledge gaps, and keep your product moving safely, swiftly, and successfully through every phase of its lifecycle.

The Eurofins Medical Device Services (MDS) network of laboratories delivers the deep regulatory insight, technical rigour, and collaborative mindset needed to meet those demands. Our consulting teams bring years of hands-on experience across device classifications, helping manufacturers align with regional and international requirements—without losing momentum.

We provide a custom-made service throughout the entire lifecycle of your product. At design validation, we define project plans and manage Verification & Validation (V&V) protocols, execution, and reporting for robust regulatory submissions. For technical documentation, we prepare and maintain comprehensive dossiers and quality systems to meet expectations before and after submission. Usability and risk analysis are integrated into a broader risk management strategy, ensuring risks from design, use error, and ergonomics are well understood and mitigated. In the pre-clinical phase, we advise on optimising your testing strategy, including chemical characterisation, biocompatibility, toxicological assessments, and absorption profiling. Our clinical evaluation support includes tailored Clinical Evaluation Plans & Reports, presenting your evidence and strategy clearly for regulatory authorities. Post-approval, we provide QA/RA support, including system maintenance and audit readiness, keeping your device compliant and competitive.