Over the years, Creanova’s team has grown to be a dynamic and international team of professionals united in the technical excellence and healthcare experience.
With the pleasure of being one team and sharing positive energy, hand in hand we are assuring that projects move seamlessly through all phases of medical devices’ development and striving for being excellent and trustable partners for our clients.
We focus on manufacturing in Europe, sourcing as many components as possible from our trusted European supply chain.
Our plant in Como, Italy is fully integrated with our Design Development Team—an added value that ensures agility, seamless communication, and efficiency. This site is ideal for prototypes, small batches, and startups as they move from concept to production.
Our plant in Stara Pazova, Serbia specializes in mid- to high-volume production (+10.000 devices per year).
Here, you benefit from competitive labor costs while keeping manufacturing within Europe—avoiding the need to source in Asia. This facility is also perfectly suited for startups scaling up production reliably and sustainably.
Low volume: up to few thousands
Full integration with R&D team
High flexibility, ideal for Startups & pilot runs
Mid/high volume: +10.000 – ca. +/-100.000 devices/ disposables yearly
Continuous production capacity
Cost-efficient European manufacturing vs Asia Clean Room
With Creanova, certifications translate into real value for you.
From fully validated processes that simplify compliance to certified infrastructure that accelerates time-to-market, we give you the tools to move faster and safer. Add the reassurance of a reliable partner and the strength of globally recognized certifications, and you gain a true competitive edge in international markets.
Our certification ensures that every contract manufacturing process complies with rigorous quality management systems for medical devices.
This translates into fully compliant products, smooth audits, and a safe path to market.
We guarantee that the devices we design and produce are safe, reliable, and compliant with global standards required by FDA and MDR, reducing non-compliance risks and accelerating regulatory approval.
Our certified cleanrooms ensure maximum control of particulate contamination, a critical requirement for complex medical devices and patient protection.