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EU medical devices regulation
Solicitors Journal

EU medical devices regulation

The EU’s proposed orphan and breakthrough device designations would formalise accelerated regulatory pathways for high-need medical technologies, with significant implications for conformity assessment, clinical evidence thresholds and notified body obligations under the MDR and IVDR
IAA shines light on first report
Solicitors Journal

IAA shines light on first report

The Immigration Advice Authority (IAA) has published its first Annual Report, marking a significant milestone as the organisation enters a new chapter under fresh leadership
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