Our Quality System

We establish & implement a quality policy that makes our basic goal; satisfaction of its customers. We have a fully documented system & every aspect of the process, activities, and operations involved with medical device and its safety and effectiveness is monitored.

We are running through a quality system & a totality of management which ensures that products are consistently produced and controlled to the quality standards appropriate to their intended use and as required by the Marketing Authorization & product specification, through:

• • Continuous monitoring of the quality management system

• • Maintaining the qualified and validated status

• • Implementation of a review system in the form of self-inspections

• • Involvement of the suppliers and service providers in the system, specific requirements monitoring Inspections and tests that were carried out through the whole life cycle of the product including raw material, in process control, and final product inspections against international guidance and standards, ensure the integrity of the product quality, safety, efficacy.

Continuous research and development retain ‘state of art’ to all of the products introduced to the market. We have been following many different techniques and concepts to improve product quality including GMP, Zero Defects, TQM, Quality Management Systems (EN ISO 13485), and various international regulatory requirements.