EUROLAB laboratory provides testing and compliance services within the scope of ISO 14937 standard. This standard specifies general requirements for the characterization of a sterilizing agent and the development, verification and routine monitoring and control of a sterilization process for medical devices.
It is applied to sterilization processes where microorganisms are inactivated by physical and/or chemical means and is intended to be applied by process developers, sterilization equipment manufacturers, medical device manufacturers to be sterilized, and organizations responsible for sterilizing medical devices.
ISO 14937 specifies the elements of a Quality Management System necessary to ensure proper characterization of the sterilizing agent, the development, validation and routine monitoring and control of a sterilization process.
EUROLAB assists manufacturers with ISO 14937 test compliance. Our test experts, with their professional working mission and principles, provide you, our manufacturers and suppliers, the best service and controlled testing process in our laboratories. Thanks to these services, businesses receive more effective, high-performance and quality testing services and provide safe, fast and uninterrupted service to their customers.
To get an appointment, to get more detailed information or to request an evaluation, you can ask us to fill in our form and reach you.
EUROLABreporting and certification activities, United Accreditation Foundation (UAF), Turkish Accreditation Agency (TÜRKAK) ve Enterprise Accreditation Foundation (EAF) based on the accreditation provided by the accreditation body. The Enterprise Accreditation Foundation (EAF) accreditation body is also a signatory of the United Nations (UN GLOBAL COMPACT) organization.
