![]() ![]() Defined on the basic principles of ISO 9001 and specific industry requirements, this standard is an effective tool for manufacturers to implement a quality management system that includes the entire process of design, development, production, installation and supply of medical devices. ISO 13485 is the international standard for the certification of a Quality Management System for the medical device industry. ![]() ISO 13485 certification to ensure safe and quality medical devices for the global market
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