FREE WEBCAST
Best Practices for Achieving EU MDR Compliance
Let your processes work for you
WHAT IS THIS WEBINAR ABOUT
Although the effective date of the Regulation (EU) 2017/745 has been delayed to 26 May 2021, medical device companies are still facing major changes. However, the regulation represents not only a compliance challenge but also a huge chance for a company-wide approach. If you want to know what companies need to do to become EU MDR compliant, this webcast fits perfectly.
The 45 minutes presentation deals with the main topics of the regulation and the latest updates and developments. The webcast will focus on device registration, Unique Device Identification (UDI) data management, product labeling and the handling of master data. Learn why an integrated, model-driven, and flexible Master Data Management (MDM) platform can provide the functionality needed to meet compliance requirements.
After the presentation you will have the opportunity to raise your questions to the presenter.
Please note that only persons with a company email address can register.
TARGET GROUP
This course will be especially beneficial to employees who are:
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UDI Team Members
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Product Labeling Team Members
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Global Strategy Business Managers
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Regulatory Affairs/Operation Leaders
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Product Managers and Business Analysts
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Manufacturing, Operations, and Supply Chain Leaders
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Quality Leaders
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Medical Device IT Support Personnel
SCHEDULES
The webinar is scheduled on the following dates:
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March 16, 04:30pm CET
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March 25, 10:00am CET
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April 13, 04:30pm CET
WHAT YOU WILL LEARN
Participants will gain insights into:
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Holistic overview of the latest developments of EU MDR
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Compliance challenges of the medical device industry
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Learning for your daily business
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Harmonization of substrate and printer
PRESENTER
Volker Watzke
EU Medical Devices Sector Manager, Domino
Volker has been part of the Domino organisation for over 10 years. He worked in different commercial roles with a strategic focus on Life Sciences in Germany. Since October 2016, Volker is part of the Domino Global Sector Management Team. Due to his long professional experience in this industry, he is an expert in the EU Medical Device Regulation.
