Awareness of The In Vitro Diagnostic Regulation On-Demand Training Course
The In Vitro Diagnostic Regulation (IVDR), is a comprehensive set of European Union (EU) rules that govern the production, sale, and distribution of in vitro diagnostic devices. These devices play a crucial role in analyzing human samples, like blood or tissue, outside the body, providing essential data for medical diagnoses and treatment planning. This short course will focus on how the IVDR prioritizes safety, effectiveness, and the highest standards of public health within the EU.
Having a consistent level of awareness across an organization can support employees to make informed decisions, enabling them to navigate complex situations with clarity and confidence.
On-demand - training that’s even more flexible
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.
How will learners benefit?
This course will help you and your teams to:
- Understand the regulatory framework for In Vitro Diagnostic Devices in Europe
- Recognize the commercial advantages of obtaining the CE Mark as evidence of conformity with the IVD Regulation
- Identify actionable steps you can take to ensure compliance with the IVD Regulation and how it can benefit you
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Upon completion of this course, learners will be able to:
- Explain how In Vitro Diagnostic Devices are regulated in Europe
- Describe the commercial benefits of the CE Mark demonstrating conformity with the IVD Regulation
- Suggest actions you can take to help with compliance to the IVD Regulation
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All staff working in relation to the IVDR.
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On completion, delegates will be awarded an internationally recognized BSI training course certificate.
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Explore our BSI Academy knowledge bundles, giving you great savings across multiple courses and an opportunity to maximize your training budget.
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