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Webinar
Medical Devices
Understanding the QMS requirements under the IVD Regulation
Rigorous regulatory controls.
This webinar:
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Manufacturers of IVD devices selling into Europe.
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Meeting regulatory requirements and maintaining a Quality Management System (QMS) under IVDR.
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Support your preparation for an efficient transition or initial certification.
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Requirements of the Quality Management System.
Contributors
For manufacturers of IVD devices selling into Europe
Key changes for meeting regulatory requirements and maintaining a Quality Management System under the IVDR for transition or initial certification.
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Contributor
Judith Prevoo
Regulatory Lead NL, BSI
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