INSTALLED MORE THAN 800 UNITS EVERY YEAR
ISO 13485 is designed to be used by organizations involved in the design, production, installation and servicing of medical devices and related services. ISO 13485:2016 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 and applicable regulatory requirements
Good Manufacturing Practice (GMP) is a term that is recognized worldwide for the control and management of manufacturing, testing and overall quality control of food and pharmaceutical products. GMP takes quality assurance approach, which ensures that products are consistently produced and controlled to the quality standards.
A CE Mark is a symbol that must be affixed to many products before they can be sold on the European market. The mark indicates that a product:
ISO 14001 is the international standard that specifies requirements for an effective environmental management system (EMS).