Polfa has a Quality Management System in place. This system is implemented and maintained to ensure the quality of the product at every stage of its manufacture, starting with the purchase of raw and packaging materials, through production, quality control, storage and distribution.
Polfa holds certificates issued by TÜV NORD attesting that the Company has introduced and applies a Quality Management System according to ISO 13485 and ISO 9001 for the design, development, manufacture and distribution of medical devices.
The company has also obtained the right to CE mark its products in accordance with the requirements of Directive 93/42/EEC.