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This intensive course enables manufacturers to learn about the key requirements, concepts and the overall process for post-market surveillance and vigilance under the MDR and IVDR.
BSI’s on-demand courses are market-leading and available 24/7
Developed by top subject matter experts, they contain the same high-quality content you will find in our tutor-led training, but with the added benefit of being able to learn at your own pace and at any time.
The course will help you:
Please note: The eLearning training lasts approximately 4-5 hours and is in English.
Benefits of On-Demand for the individual
Convenient - courses are available 24/7 and you can learn at any time and from any place that suits you – you just need an internet connection
Learning pace - You can learn as fast or as slowly as you want to. You can also take breaks at any time in the course and pick up where you left off when you are ready to continue
Information retention - During the access period, you can go back and repeat parts or all the course to refresh and reinforce what you have learned
High-quality materials - Developed by top subject matter experts, course content is both detailed and engaging, with explanations, activities, and knowledge checks to enhance your learning
On completion of this training, you’ll be able to:
This course is ideal for you if you’re in a quality assurance/quality control/regulatory/patient safety/customer facing role involved in continuous improvement and customer advocacy.
Delegates should have a basic understanding of European Medical Device and In-vitro Diagnostic Regulations (MDR).
On completion, you’ll be awarded an internationally recognized BSI Training Academy certificate.
Participants:
Sprechen Sie uns an und erfahren Sie, wie wir Sie auf Ihrem Weg zu nachhaltigem betrieblichen Erfolg unterstützen können.