Quality System
Medical Products Research focuses on the design and the production of reliable products for its clients.
Through its implementation of the Quality System at company level, according to the UNI EN ISO 13485:2016 norms, MPR undertakes to fully satisfy clients’ expectations - in particular to guarantee the excellence of each single product to the final users.
Thanks to an effective business management system, the quality of our products is constantly controlled and certified.
We respect the needs expressed by our clients and by those who work in connection with our activity, and we pay great attention to try and develop new methodologies, researching new potential clinical applications for the products, and providing staff training on new devices and techniques.
Moreover, MPR is committed to improving its own methods and work procedures in order to achieve flawless products.
We respect the needs expressed by our clients and by those who work in connection with our activity, and we pay great attention to try and develop new methodologies, researching new potential clinical applications for the products, and providing staff training on new devices and techniques.
Moreover, MPR is committed to improving its own methods and work procedures in order to achieve flawless products.
The company direction believes that it is possible to achieve a high quality of products only if all who work in and for the firm are committed to obtaining an improved work organisation and reducing the non-quality costs. Furthermore, we consider the promotion of work safety and health an essential part of our task as company directors. MPR is also aware that the success of the company is linked to the achievement and continuous improvement of a high standard of Environmental and Health protection regarding the local community where the company operates.
Adherence to the UNI EN ISO 13485:2016 standard is voluntary, but it represents a quality requirement for medical device manufacturers whose responsibility it is to systematically provide effective and safe products.
Adherence to the UNI EN ISO 13485:2016 standard is voluntary, but it represents a quality requirement for medical device manufacturers whose responsibility it is to systematically provide effective and safe products.
