OUR QUALITY POLICY
Our general policy takes into account market data as well as regulatory aspects and our commitment is therefore to :
Implement and maintain the efficiency of a quality management system that conforms to the EN ISO 13 485 : 2016 norm.
Meet the requirements of the CE 93/42 directive dd June 14, 1993 covering the CE mark of our products and maintain the surveillance of incidents and incident's risks that may result from the use of the sterile medical devices after their launch on the market.
Since our quality policy must be adapted to our organization, we regularly carry out reviews in order to verify its adequacy to our needs
At JCM MED, we manufacture our sterile devices in different parts of the world. We regularly carry out audits of the Quality Management system and of the manufacturing premises, so that to ensure that the products are best manufactured in those locations. The QM System is certified against the ISO 13485 standard and all our sterile devices are CE marked. The products are manufactured in ISO-7 and ISO-8 class clean rooms.
JCM MED is based in France and its sister company, JCM MED Limited is located in Hong Kong.
OUR QUALITY POLICY IS THEREFORE TO MAINTAIN AND IMPROVE:
The safety of our products
The quality of our products and services
The quality of our suppliers
Our customer’s satisfaction
Our international recognition