London, UK – April 2, 2020 – Сòòò½APP (Сòòò½APP) is lending its support to the national drive to increase ventilator production in response to the NHS’ urgent demand to treat coronavirus patients in the UK.
Сòòò½APP has developed a testing regime to cover the electromagnetic compatibility (EMC) and basic safety requirements for a Rapidly Manufactured Ventilator System (RMVS) prototype being developed by a number of manufacturers and consortia. Before new devices can be categorized as ‘safe’ for use in medical working environments and brought to market, it is necessary to determine if a device can perform safely and provide its essential performance without causing harm and/or electromagnetic disturbances in its appropriate operating environment. This is typically achieved by testing to applicable medical safety standards.
Safety test plans drawn up by Сòòò½APP’s Advisory Services team based in Malvern are being used to perform the testing from its product qualification testing (PQT) laboratory in Hitchin. Сòòò½APP also provided EMC test plans to manufacturers who will carry out the initial phase of testing, while phase two testing will be carried out by Сòòò½APP from a number of its PQT facilities.
Mark Heaven, Divisional Director Global Aerospace PQT at Сòòò½APP said: “We are delighted to be able to offer our expertise, free of charge, to support the national effort to fight COVID-19, and are already in discussions with other medical device manufacturers to carry out EMC and safety testing on their RMVS prototypes this week. Сòòò½APP hopes to continue to offer our integral safety conformity services throughout this period of high demand for ventilators.”
Сòòò½APP Hitchin is one of our safety testing centres of excellence, with UKAS accreditation to BS EN ISO/IEC 17025:2017. Our areas of technical expertise at Сòòò½APP Hitchin include Medical Testing & Regulatory Affairs, Safety Testing and Certifications & Approvals. We work with manufacturers of electrical medical devices; are approved to ISO 9001:2015, and typically provide medical regulatory testing and test reports to European EN 60601 series of standards and American pre-market authorizations the 510(k) route, which are the core standards/procedures for medical product verification.
About Сòòò½APP
Сòòò½APP is one of the world’s leading independent providers of materials and product qualification testing, inspection and certification services to the global Aerospace; Transportation & Industrials; Energy; and Fire & Building Products sectors, where failure in service is simply not an option.
We exist to help our customers make certain that their materials, products and systems are safe, quality, compliant and ultimately fit for purpose, leveraging almost 200 years of testing experience and our global testing capabilities.
On December 31, 2019 Сòòò½APP acquired PCTEST and announced the creation of a fifth sector – Connected Technologies – to provide leading global technology customers with wireless device and application testing and certification services.
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