UK | Medical Device Post-Market Surveillance Regulation (in force 16 June 2025)
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SWITZERLAND | swissdamed UDI Module Goes Live — Mandatory Device Registration from July 2026
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BRAZIL | UDI System Goes Live for High-Risk Medical Devices
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AUSTRALIA | TGA Mandates Hospital Reporting & UDI System — Implications for Device-Based Real-World Research
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EU | Implementing Regulation (EU) 2025/1466 Tightens Execution of PV Obligations
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CZECH REPUBLIC | Cybersecurity Act Implements NIS2 — New Compliance Obligations for Health Research
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BRAZIL | Implementation Update – Law 14,874/2024 and SINEP
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UK | MHRA Retains Critical Medical Device Regulations Following Overwhelming Industry Support
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UK | Health Research Authority’s Strategy 2025-28: A New Era for Real-World Evidence and Clinical Research
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