#MDR

Urgent Need to Revise the Medical Devices Regulation
by chemsafe|29 Ottobre 2024|Blog, Medical
The resolution on the urgent need to revise the Medical Devices Regulation, presented by several...
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Prorogation for submission and authorisations of DEHP application for MD and IVD
by admin|28 Novembre 2023|Medical
Where we stand with MDR and IVDR European regulations about Medical Devices (Reg. EU 2017/745)...
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MDR avanti adagio: Eudamed vedrà la luce nel 2024
by admin|7 Novembre 2022|Medical
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Borderline products
by admin|24 Maggio 2022|Medical
[vc_acf field_group="1287" field_from_1287="field_5a155fb5628a4"] [vc_acf field_group="1287" show_label="yes" field_from_1287="field_5a1538a612368"][vc_acf field_group="1287" show_label="yes" field_from_1287="field_5a15385612367"][vc_acf field_group="1287" show_label="yes" field_from_1287="field_5a1539cf1236a"] [latest_post type="minimal"...
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