MDCG 2020-3 Rev.1: Clarifying Transitional Provisions under MDR Article 120 for Legacy Medical Devices
August 22, 2023
MDCG 2020-3 Rev.1: Clarifying Transitional Provisions under MDR Article 120 for Legacy Medical Devices
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August 22, 2023
MDCG 2020-3 Rev.1: Clarifying Transitional Provisions under MDR Article 120 for Legacy Medical Devices
August 22, 2023
Commission Guidance on the Content and Structure of the Summary of the Clinical Investigation Report
August 22, 2023
Ensuring Biocompatibility Compliance for Medical Device Instruments in the UK: A Guide to MHRA Requirements
August 17, 2023
Cybersecurity for Medical Devices in the UK
August 15, 2023
The appointment of an EU Authorized Representative (EU AR) is a significant challenge for manufacturers outside the European Union (EU) seeking to enter the EU market.