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This intensive course enables greater understanding of the key requirements for technical documentation for IVDs, in line with the European IVD Regulation (IVDR) requirements in Europe.
A required part of conformity assessment and CE Marking is the need for Technical Documentation which includes the collation of supporting information about your IVD Device. Technical documentation is maintained throughout the product lifecycle. Learn how to assemble this and other types of required information so you can CE Mark your device in Europe.
This course will help you learn:
Expectations of Notified Bodies for technical file content during reviews, both at launch and during the product lifecycle
Upon completion of this training, you will be able to:
Recognize the documentation requirements during the product lifecycle and the post market updates needed
QA/Regulatory personnel involved in compiling technical documentation and design dossiers. Product design personnel and those in Research & Development for IVDs intended for the European market.
On completion, you'll be awarded an internationally recognized BSI Training Academy certificate
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