EU: Notified Body designation renewal process to be eased temporarily
EU: Guidelines on the adoption of Union-wide derogations for medical devices
EU: Guidance documents from the MDCG
EU: Continued use of mercury in electric rotating connectors used in intravascular ultrasound imaging systems likely to be permitted until June 2026
EU: Help provided on adapting IT systems to implement new MIR form; enforcement dates for use of IMDRF codes and terms
EU: CEN/CENELEC reject Commission’s standardisation request for the MDR and IVDR
Spain: Return to usual procedure for importing medical devices
Spain: AEMPS launches CERTPS application system for Certificates of Free Sale
Spain: Deadline extension for Brexit labelling changes
UK: Updated information on when apps are considered medical devices
UK: New guidance published on writing and distributing effective FSNs
UK: Latest regulatory guidance issued in relation to COVID-19
UK: Independent review of device safety recommends reforms to MHRA and establishment of a registry like the Australian ARTG
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