Pacific Medical Systems Limited receives ISO 13485 certification.

ISO 13485 is to facilitate harmonised medical device regulatory requirements. It is designed to be used by organizations involved in the design, production, installation and servicing of medical devices and related services and it ensures that all medical devices meet the proper regulatory compliance laws and customer needs. While presently not compulsory for a medical devices distributor in Hong Kong, the certification helps in satisfying and aligning our Medical Devices Quality Management System with those of our global suppliers and trading partners.