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Supporters & Partners
Educational Methodology
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IVDR Medical Device Conformity Assessment Training
On-Site Trainings
MDR / IVDR from the Distributor’s Perspective
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Magyar
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What Are the responsibilities of a Site Auditor, a Product Reviewer and a Clinical Expert?
IVDR: The Transitional Period Has Been Extended!
MDR: The Transitional Period for Legacy Devices Has Been Extended!
The 3 Most Common Reasons for MDR Application Rejection