Act Now to be Ready on Time – Guide to New Classification Rules for In Vitro Diagnostic Medical Devices
Continuing our series of publications, we outline the key changes to the classification of in vit...
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Continuing our series of publications, we outline the key changes to the classification of in vit...
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The Protected Disclosures (Amendment) Act 2022 has now been signed into law and will significantl...
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The EU has proposed amendments to the Benchmarks Regulation to address issues arising from the co...
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On 6 January 2020, ESMA published its Level 3 Guidelines for compliance with the obligation to re...