COGS reduction
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Boosting R&D Productivity Amid Complex Regulations
MedTech manufacturers like you face converging operational and strategic pressures demanding bold transformation. The need to comply with a complex set of regulations, such as Europe’s MDR, is slowing development by creating bottlenecks in the validation process. At the same time, tight price targets are squeezing margins.
The shift from standalone devices to connected care adds new layers of complexity, requiring robust capabilities in software validation and data management. Concurrently, R&D productivity is declining. These challenges require more than incremental fixes. We work alongside MedTech leaders to build future-ready systems, streamline global operations, and integrate R&D and manufacturing. We help you accelerate performance and navigate compliance, ultimately turning these operational constraints into a powerful competitive advantage. EFESO stands beside you the entire way, from the boardroom to the factory floor.
Real Results Achieved with our Clients
EFESO helps MedTech leaders accelerate performance. Streamline global operations, integrate R&D and manufacturing and navigate compliance to deliver:
Lead time compression
Productivity gains
A Tailored and Pragmatic Approach that Fits your Reality
Your MedTech transformation begins where complexity meets opportunity. EFESO collaborates with your teams to accelerate approvals, stabilize supply chains, and enable connected care.
We align operational excellence, compliance, and digital development across R&D, QA, and production. From a validation strategy to a smart factory deployment, we embed continuous improvement for scalable, measurable and lasting performance gains.
Our Services to Support your Transformation
Explore how our actionable, high-impact and tailored service offerings help you succeed
The EFESO Touch
MedTech operations demand both unwavering precision and transformative change. EFESO works directly on your production floors, applying our experience from over 200 medical device implementations to navigate complex regulatory landscapes. We embed FDA and MDR requirements into every improvement, consistently achieving 8-12% COGS reductions without compromising quality.
We don’t just design strategies; we implement them with you, transforming compliance into value and driving long-term performance in MedTech manufacturing.
From boosting R&D productivity to enabling mini-factory transformations, we build lasting capabilities within your teams. Our approach combines hands-on execution with digital readiness, ensuring sustainable impact. The results speak for themselves:
Meet Some of our MedTech Team Members
Ready to Revolutionize Patient Care?
- Bring breakthrough devices to market faster
- Balance innovation with regulatory excellence
- See MedTech pioneers cutting development cycles in half