Here at Trident, our work is based on consistency, experience and discipline. We work as a team to achieve an objective: to make progress, together. Our aim is for each individual to be able to give his or her very best on the job, and for this to be reflected in the quality of the products developed. Only in this way can we guarantee our customers the best possible service as a business, offering solutions as well as products. We are ready to invest every drop of our potential, knowledge and human qualities in complying with this mission.
Here at Trident, our administrative and manufacturing processes are endorsed and certified by the competent bodies in charge of continually monitoring the company’s conduct, so customers can rest assured that all our manufacturing and customer service departments are continually being assessed and are improving all the time. Each of our products undergoes stringent quality controls throughout the manufacturing process, and is exhaustively tested before it leaves the factory. This is the only way to ensure our customers receive the quality they deserve.
IMQ, Istituto Italiano del Marchio di Qualità, an Italian certification body and a European leader in conformity assessments and laboratory tests for the electrical, electronic, gas and energy industries, has verified and accredited the Administrative Processes and Procedures in Trident.
ISO 13485. This standard adopted by CEN as EN ISO 13485:2003/AC:2007 is harmonized with respect to the European medical device directives 93/42/EEC, 90/385/EEC and 98/79/EC. ISO 13485:2003 specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer requirements and regulatory requirements applicable to medical devices and related services.