ISO 14971:2019 – Does your Risk Analysis meet this new revision of the Standard?
Start Date: 2021-04-22
End Date: 2021-04-22
Time: 10:00 am to 1:00 pm
This webinar will benefit medical device companies planning to have a CE mark under the European Union Directive 93/42/EEC. We will discuss what is new in ISO 14971:2019 and help you avoid delays in obtaining or maintaining your CE mark for compliance to the Medical device Directive, EU Directive 93/42/EEC on Medical Devices.
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Organized by : Complianceonline