GOLDWIN has always laid utmost emphasis and efforts into implementation and uplifting the principles of Good Manufacturing Practices (GMP) as well as following Quality Systems in accordance with ISO 9001/EN ISO 13485.  As a manufacturer of medical devices, the company is committed to provisions such as Council Directive 93/42/EEC and products in compliance with this Directive can be identified by the CE mark.  All this is possible due to the commitment of the company personnel as every member understands and accepts the responsibility of producing GMP products that are ‘safe for use and of the highest quality’.