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Within UL Solutions we provide a broad portfolio of offerings to all the medical device industries. This includes certification, Approved/Notified Body and consultancy services. In order to protect and prevent any conflict of interest, perception of conflict of interest and protection of both our brand and our customers brand, we have processes in place to identify and manage any potential conflicts of interest and maintain impartiality. UL Solutions is unable to provide consultancy services to EU MDD, MDR or IVDD Notified Body, UKCA MD Approved Body or MDSAP Customers.
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Factory Retooling

Solutions to help you adapt your processes and factory to meet the global demand for masks, ventilators and other key products.

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As the demand for ventilators and other life-saving medical equipment grows in the current COVID-19 environment, manufacturers need to pivot to help meet the global demand.

Factory retooling in times of crisis is not a new concept. Just as automotive manufacturers transitioned from creating cars to aircrafts in the 1940s, in 2020 manufacturers are tasked with retooling their factories to create ventilators and other medical devices.

At UL Solutions, we provide a complete suite of services to support manufacturers who are adapting their processes and factories to meet this extraordinary need. Our Field Evaluations assist manufacturers with factory retooling plan reviews and on-site evaluations to verify compliance and check for critical safety issues as machinery is retooled and manipulated. We also offer medical equipment and device audits to ISO 13485, the internationally recognized quality indicator that demonstrates the ability to provide medical devices and related services.

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