Our Mission and Expertise
At MediB, we are dedicated to guiding medtech innovators through the complex landscape of European market regulations. With our in-depth knowledge of development, CE certification, and regulatory strategy, we help turn innovative ideas into fully compliant and market-ready products.
CE Certification Simplified
Navigating the intricacies of CE certification can be daunting. At MediB, we simplify the process, ensuring that your products meet the necessary standards for market entry, giving you a competitive edge.
Regulatory Strategy Tailored to You
Every medtech innovator has unique needs. Our tailored regulatory strategies are designed to align with your specific product and market goals, providing you with a clear pathway to success.
Market-Ready Product Development
Bringing a product to market involves numerous challenges. With MediB as your partner, we streamline the development process, ensuring that your product meets regulatory requirements and is ready for market launch.
Focused on Your Growth
At MediB, we are committed to simplifying EU regulations so that you can concentrate on the growth and expansion of your medtech innovations, confident in the compliance and market readiness of your products.
Strategic Support for MedTech Innovators
Experience and Facts
20
Years of Experience
50+
Medtech Partners
30+
Market-Ready Products
€2.1B
In 2023 European Startups secured signifecant funding
500K
Medical Devices in the EU Market
Our Collaborative Network
