Performance Evaluation and Clinical Evidence for IVDs On-demand

Level Specialist Duration 3.5 hours

Available to book: On-demand elearning £570 + VAT Book your place

If you are involved in planning, conducting or documenting performance evaluation and clinical performance studies for IVD devices in Europe, this intensive one-day course will enable a greater understanding of performance evaluation for In Vitro Diagnostic devices under the IVD Regulation, how performance fits into the product development lifecycle and IVD Regulation (IVDR) requirements for clinical evidence.

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 I benefit?

This course will help you:

Learn what an In Vitro Diagnostic is and what is required to demonstrate performance according to the IVD Regulation
Appreciate what the design and development stages are during IVD product development
Understand the definitions of performance evaluation that incorporate clinical evidence under the In Vitro Diagnostic Regulation
Identify the analytical performance studies required
Explore clinical performance studies including the legal and regulatory requirements and practical considerations
Document clinical evidence and maintain the documentation throughout the life cycle of the product

Upon completion of this course, learners will be able to:
- Appreciate the need for performance evaluation and how it fits into product development under the IVD Regulation
- Learn key definitions of performance evaluation and clinical evidence under the IVD Regulation
- Gain awareness of the scope of the European regulatory requirements for IVD clinical performance studies under the IVD Regulation
- Distinguish between non-invasive and interventional clinical studies and understand requirements for vulnerable and protected study subjects
- Apply practical considerations for study design and protocols
QA/Regulatory and R and D scientists involved in planning, conducting or documenting performance evaluation and clinical performance studies for IVD devices in Europe.
On completion, you’ll be awarded an internationally recognized BSI Training Academy certificate.

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