Client Success Stories: Proven Regulatory Solutions for MedTech & IVDs
Real Results. Trusted Partnerships. Audit-Ready Outcomes.
Navigating Regulatory Classification with Confidence
See how C the Signs established a clear, defensible regulatory pathway for UKCA and CE marking without hiring internal regulatory staff. By partnering with SciMed, they secured dual-market classification rationales, reduced in-house burden, and accelerated compliance timelines; freeing their team to focus on innovation, not interpretation.
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.