You can find our seminar presentation on Clinical Research in Medical Devices, which we organized on January 28, 2021, to inform industry stakeholders, in the rest of this article.
Whether the potential risks of a medical device are at an acceptable level is determined by comparing them with the benefits it provides for its intended use.
Activities Requiring Notification for Medical Devices
In order to meet MDR requirements and demonstrate product conformity, manufacturers must prepare the reports listed below periodically and ensure that they are up-to-date.
By default we only use cookies to remember your settings.
If you allow statistics cookies, you will see non-personalized ads.
If you allow marketing cookies, you will see personalized ads.
For more info see our privacy policy.
