Client Success Stories: Proven Regulatory Solutions for MedTech & IVDs
Real Results. Trusted Partnerships. Audit-Ready Outcomes.
Achieving EU MDR Compliance at Scale
Discover how Caristo Diagnostics have been achieving seamless EU MDR compliance since 2019 without hiring internal clinical staff. By partnering with SciMed, they secured 100% CER approval rates, streamlined updates, and reliable audit readiness—while focusing their resources on innovation, not regulation.
Explore how leading medical device and IVD companies have achieved compliance, scaled regulatory activities, and navigated complex EU and UK requirements with SciMed's expert support.
These case studies highlight:
Practical solutions for MDR and IVDR compliance challenges
Scalable strategies that support growth without expanding internal teams
Evidence of long-term value through post-market support and clinical evaluations
Whether you're preparing a Clinical Evaluation Report or building a Post-Market Surveillance strategy, see how others have made it work; with SciMed by their side.