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How efficient is your product process?
In the event of a product recall it is essential that manufacturers, suppliers and NHS providers are able to identify and locate the product as quickly as possible, in order to limit potential harm to patients.
Using Unique Device Identifiers (UDIs) for medical devices means that these products can be easily be tracked and traced, and removed from circulation efficiently.
Join us at this joint MHRA and GS1 UK Webinar and find out how you can improve your processes. There is also the opportunity for you to pose your questions.
Webinar: UDIs in Field Safety Notifications and MHRA Medical Device Alerts Date: Wednesday 3 December 2019 Time: 11:00-11:45
We look forward to having you join us.
The Medicines and Healthcare products Regulatory Agency
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