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ISO 20916 is a new standard addressing requirements for clinical performance studies on IVD medical devices.
Clinical performance studies using specimens from human subjects — Good study practice.
Planning, design, conduct, recording and reporting of clinical performance studies.
Assessing the clinical performance and safety of IVD medical devices for regulatory purposes.
Standard ISO 20916 In vitro diagnostic medical devices.
Information presented within this webinar is based on our current understanding of the IVDR standards.
IVD Training Lead, BSI.
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