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IVDR: Questions and answers


Questions and answers relating to the Transitional Provisions of EU REGULATION 2017/746 (IVDR) on in vitro diagnostic medical devices

Version: 01 November 2022

You are welcome to request our FAQ catalog on the IVDR topic from us. In it, we provide detailed answers to relevant questions.

Please contact us at immunhistochemie@zytomed-systems.de.

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