Production of medical devices and hygienic products involves responsibility for safety of their users and of the environment.
Being fully aware of it, we implement actions that ensure safety of our products and meet legal and normative requirements at each stage of manufacturing, starting with the design, selection of materials and packaging, up to all production stages and storage.
At our production sites we have implemented international quality and safety standards: ISO 9001, ISO 13485 and ISO 14001, therefore, we undergo regular audits performed by renowned certification bodies.
The design process takes into account legal requirements, including MDR and REACH, environmental requirements and safety parameters throughout the entire product life cycle. Each product undergoes a detailed risk analysis and quality assessment.
Raw materials, auxiliary materials and technological equipment used meet the highest quality requirements. Each production process is controlled, and quality of the product is verified at each manufacturing stage. For each process, we identify hazards in terms of product and environmental safety, which allows us to implement effective measures to prevent their negative effects.
Being aware of importance of the process hygiene for safety of the product, our products are manufactured in plants with cleanliness controlled at production rooms. As we have a microbiological laboratory at our disposal, we can quickly verify quality and cleanness of raw materials used and of manufactured products, as well as their production environment. Furthermore, we continuously improve knowledge and awareness of our employees on how the hygiene of the process and personnel translates into product safety.
Polimery
