Our Team
Our international team brings together expertise in medical device design, engineering and manufacturing, combining technical knowledge with a shared commitment to improving healthcare.
Through close collaboration across disciplines, we support our clients throughout medical device development, from the initial concept to production. A collaborative approach, clear communication and attention to detail help us build lasting partnerships and keep projects moving forward.
Leadership Team
Design & Development Team
Caetano Lobo
Head of Design & Development
Michele Broggio
Lead Product Engineer
Sara Galfrascoli
Lead Product Designer
Davide Quagliani
Senior Product Designer
Giulia Orazia Cicciarella
Product & UX/UI Designer
Samuele Montorfano
Senior Product Designer
Enrico Zatti
Lead Product Engineer
Virginia Doria
Product Engineer
Rohit Rana
Product Engineer
Giovan Battista Basile
Senior Product Engineer
Tatiana Palombi
Senior Product Engineer
Giovanni Ghiggi Perone
Senior Product Engineer
Production Team
Miloš Maričić
Production Plant Director
Alessandro Capella
Production Manager
Simon Pernettaz
Product Engineer
Roselie Brussen
Manufacturing Lead
Tijana Erac
Manufacturing Process Engineer
Nikola Karačov
Manufacturing Process Engineer
Matteo Albertolli
Quality Control & Assembly Specialist
Nikolina Tomić
Quality Control Responsible
Vukašin Knežević
Assembly Manager
Assembly Team
Logistics & Purchasing Team
Miloš Prodanović
Logistics Specialist
Martina Redaelli
Purchasing Specialist
Tamara Krsmanovic
Purchasing Specialist
Milana Borovac
Administration Specialist
Our Innovation Hub
We combine medical device design, development and manufacturing in Europe, supported by a trusted European supply chain. Our facilities in Italy and Serbia support projects from prototyping and small batches to larger-scale production.
Our facility in Como, Italy, works closely with our Design & Development Team, enabling direct collaboration between engineering and manufacturing. It supports medical device prototyping, pilot runs, and small-batch production, helping startups and established companies move from concept to production.
Our facility in Stara Pazova, Serbia, focuses on medium- to high-volume medical device manufacturing, with production volumes exceeding 10,000 devices per year. Competitive production costs and a European location support companies looking to scale production while keeping development and manufacturing closely connected.
Manufacturing Plant in Italy
Via Antonio Magni 54 – Como, Italy
– Low-volume production: up to a few thousand units
– Full integration with our R&D team
– Flexible manufacturing for startups, prototypes and pilot runs
Manufacturing Plant in Serbia
Kamenjareva 34 – Stara Pazova, Serbia
– Medium- to high-volume production: 10,000–100,000 medical devices or disposables per year
– Capacity for ongoing production
– Cost-efficient medical device manufacturing in Europe
– Cleanroom assembly
Quality Certifications
Regulatory Compliance
& Certification
Creanova’s certified quality management systems support our medical device design, development and manufacturing activities. Through documented processes, quality controls and traceability, we help clients manage applicable regulatory requirements throughout their projects.
Our approach connects engineering, manufacturing and quality assurance, supporting consistent results from development to production.
ISO 13485
Our ISO 13485-certified quality management systems support medical device manufacturing through documented procedures, traceability and quality controls.
Working within the scope of our certifications, we help clients meet applicable quality requirements and prepare for audits, supporting consistent production and regulatory documentation.
Guaranteed
Quality
in Medical Device
Manufacturing
ISO 9001
Our ISO 9001-certified quality management systems support consistent processes across design, development and manufacturing. Through documented procedures, continuous improvement and a focus on customer requirements, we help deliver reliable results throughout each medical device project.
Safety &
Effectiveness
of Electromedical
Devices
ISO 14644
Our cleanrooms, classified in accordance with ISO 14644, provide controlled environments for medical device assembly and packaging. By controlling airborne particulate contamination, we help protect product integrity and support the cleanliness requirements of each manufacturing process.
Controlled
Environment
Production
European Innovation Council (EIC)
As a provider listed in the EIC Service Catalogue, Creanova supports MedTech startups with integrated medical device design, development and contract manufacturing services.
Eligible companies can explore EIC funding and support programmes, including EIC Accelerator and EIC Access+, subject to each programme’s requirements.
Explore our EIC Services and support programmes: