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Full Version: [F4LT] Build a winning strategy for EU MDR Compliance
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Build a winning strategy for EU MDR Compliance
Our experts will show you how to leverage the benefits of a successful MDR strategy
Free tutorial
Rating: 4.2 out of 5
(18 ratings)
433 students
1hr 2min of on-demand video

Description
Successful MDR compliance is demonstrated by the application of a CE-mark to the device. Class I manufacturers (except for devices that are sterile or have a measuring function) may self-apply a CE-mark after producing a declaration of conformity. For all other classes of medical device, a CE-mark may only be affixed once a Notified Body has issued a certificate of conformity following a regulatory review according to rules in Chapter IV of the MDR.

This modified webinar will allow medical device manufacturers and suppliers to benefit from our unique knowledge and insight of working with the Medical device Regulation. The lecture is aimed at suppliers and manufacturers of medical devices from across the industry, and will give you an empowering perspective on working successfully with the MDR. With our MDR Masterclass you will be able to get beneath the skin of the EU MDR and understand the key requirements for medical device compliance.

https://www.udemy.com/course/build-a-winning-strategy-for-eu-mdr-compliance/

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