Medical

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EAEU Changes Requirements to Quality Management System Assessment for Medical Devices

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EU Implements Regulations Related to Electronic Instructions  for Medical Devices

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European Union Issues Regulation Concerning Eudamed Database

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MDCG Publishes Application of MDR Requirements to Legacy Devices and Old Devices

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Saudi Arabia Updates RoHS Requirements for Electrical and Electronic Equipment

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EU Cancels Conformity Assessment Exemption Procedure for Medical Devices and Personal Protective Equipment within COVID-19 Pandemic

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Medical Device Coordination Group Introduces New Guidance for Notified Bodies, Distributors and Importers within MDR Requirements

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European Union Publishes Brochure with Frequently Asked Questions about European Medical Device Nomenclature

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European Union Establishes Clinical Investigation Application/Notification Document MDCG 2021-08

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European Commission Сreates Unique Device Identification Helpdesk

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