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The new EU Medical Device Regulation (MDR) marks a significant shift from the previous directives. This course at will cover the updated requirements of the EU MDR, focusing on essential topics such as quality systems, product classification rules, technical documentation, clinical evaluations, Unique Device Identification (UDI), and post-market surveillance. Participants will also gain insights into planning an efficient implementation of the new regulations.
By the end of the course, participants will be able to:
The This course offers this course for medical device professionals involved in quality and regulatory affairs, design, risk management, post-market activities, R&D, and manufacturing, particularly those working for manufacturers that market devices.
Upon completing the program, participants will be equipped to:
The new EU Medical Device Regulation (MDR) marks a significant shift from the previous directives. This course at will cover the updated requirements of the EU MDR, focusing on essential topics such as quality systems, product classification rules, technical documentation, clinical evaluations, Unique Device Identification (UDI), and post-market surveillance. Participants will also gain insights into planning an efficient implementation of the new regulations.
By the end of the course, participants will be able to:
The This course offers this course for medical device professionals involved in quality and regulatory affairs, design, risk management, post-market activities, R&D, and manufacturing, particularly those working for manufacturers that market devices.
Upon completing the program, participants will be equipped to:
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