Celegence (www.celegence.com/services/me...) provides the medical device industry with consulting services that are tailored to the evolving needs of manufacturers.
Our suite of services including EU MDR related support allows you to focus on your core responsibilities. With our guidance, bringing your devices to the market and keeping them there will be easier for your regulatory and quality teams.
With the EU MDR following the FDA’s lead in requiring a UDI, regulatory affairs teams must be ready to update many of their processes to be able to register their products in the EUDAMED database. Additionally, certain best practices should be followed for creating structured device registration and Unique Device Identification (UDI) data, as well as for implementing EU MDR compliant product labels in order to comply with the date of application (DoA) requirements.
During our webinar titled “Best Practices for UDI Implementation and EUDAMED Submissions”, Dr. John spoke specifically about how to register products in the EUDAMED database and various modules.
Why should you watch this webinar?
1. To understand the structure of EUDAMED and the availability of various modules
2. To learn about Actor Registration Module
3. Discussion on the process rationale and documentation
For more information on how we can help you with EU MDR reach out to us at info@celegence.com, contact us online or read more about Celegence’s medical device services.
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