Who we are
Restech Srl is a spin-off company from Milan Politecnico University, established in 2010 by the Department of Bioengineering. For several years, the department has been focusing its research effort on developing new technologies to investigate the pathophysiology of the respiratory system and respiratory medicine more generally.
Restech, starting from the academic know-how, experience and patented IP, has become a leader in developing, engineering and manufacturing innovative medical devices. RESTECH technologies allow the measurement of respiratory function in an easy and intuitive way, resulting in a patient-friendly management and monitoring of the disease.
Restech’s mission: “Highly innovative medical devices from research to new advanced and smart solutions in the respiratory sector”.
MEET OUR TEAM
Alessandro Gobbi, Phd
Founder, COO, Director of QARA, Member of the Scientific Steering Committee
Pasquale Pio Pompilio, PhD
Founder, CCO Business development director, Member of the Scientific Steering Committee
Raffaele Dellacà, PhD
Founder, Chair of the Scientific Steering Committee
Lead software engineer
Medical device internal auditor
WO2012014024 – “System and method for measuring the mechanical impedance of the respiratory system”
WO2012032402 – “System for the automatic detection of respiratory diseases and for the prediction of future acute airway instabilities”
WO03103493 – “System and method for the automatic detection of the expiratory flow limitation”
Quality and Safety
Restech wants to assure a total satisfaction of its Customers. Our Quality system is certified according to the ISO 9001 standard and aims at improving continuously the quality of its medical devices.
Our Quality system is also certified according to the ISO 13485 standard: the safety and effectiveness of the products are guaranteed by a continuous and organized monitoring of all the stages that constitute the product’s life cycle, from the design to the marketing of the finished item.
All products manufactured by Restech are compliant with the 93/42/EEC Directive on medical devices and are CE marked.