Who we are
Our mission
At Giesse Diagnostics, our mission is to enhance global healthcare by delivering innovative and reliable diagnostic solutions. Our rigorous quality control system guarantees that all products undergo thorough analytical testing in our in-house laboratories.
Our expertise
With 45 years of continuous dedication to the diagnostic medical devices industry, Giesse Diagnostics has built unmatched expertise through ongoing innovation and commitment.
Our Skills
Expertise
With 45 years of unwavering dedication to the diagnostic medical devices industry, Giesse Diagnostics has developed unparalleled expertise through continuous innovation and commitment.
Reliability
Giesse Diagnostics' commitment to quality and reliability is reflected in their compliance with UNI EN ISO 13485:2016 and UNI EN ISO 9001:2015 standards, as well as their conformity with European Union Directive 98/79/EC
Innovation
Giesse Diagnostics is committed to innovation, constantly enhancing its products through advancements in production processes and the adoption of cutting-edge technologies.
Sustainability
Giesse Diagnostics shows a strong commitment to sustainability by integrating environmentally responsible practices throughout its operations
About us
Giesse Diagnostics is a family-owned company specializing in the production of in vitro diagnostic medical devices. Founded in Rome, Italy, in 1978, it is an independent enterprise with a long history of innovation.
Initially, Giesse Diagnostics focused on producing general chemistry reagents, introducing several innovative products. This was later expanded to include immunoturbidimetry, serology, and coagulation reagents.
The quality of Giesse Diagnostics products is continually enhanced through innovations in production processes, analysis, documentation, and services.
Over the years, significant investments have been made to improve our quality management systems, which now comply with the following standards: UNI EN ISO 13485:2015 and UNI EN ISO 9001:2016. Additionally, our in vitro diagnostic medical devices comply with European Union Directive 98/79/EC.
GIESSE in the World
We embrace international challenges with confidence, addressing them through our exceptional service and expertise. Giesse Diagnostics is a market leader in quality across multiple countries and complies with European Union Regulation No. 98/79/EC
Giesse Diagnostics S.r.l.
Via Enrico Fermi, 3 - Z.I. Via Tiburtina km.18,300 00012
GUIDONIA MONTECELIO (RM)