At Transpact MedTech we believe that “Quality is not an act. It is a habit” and that Safety and quality are non-negotiables especially in medical devices industry.
Thus, by keeping all phases of production – design, manufacture and customer service – in-house, we ensure clients receive quality equipment that meets their specific needs at a reasonable cost.
Our Product meets the following quality assurance and regulation standards.
ISO 13485:2016
Our successful procurement of ISO 13485: 2016 certification is the result of our high intention, sincere effort, intelligent direction and skillful execution of stringent regulatory requirements throughout every step of a product’s life cycle, including service and delivery.
ISO 9001:2015
It is rightly said “We cannot have islands of excellence in a sea of slovenly indifference to standards.” Our pursuit for the excellent quality is reflected in the ISO 9001:2015 certification for quality management system.
CE
Our products comply with the essential requirements relevant of health, safety & environment protection legislations i.e. CE marking.