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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UK | New Amendment History Log Template
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EU | Proposed Amendments to Regulation EU/520/2012 Affecting Post-Authorisation Safety Studies
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LUXEMBOURG | New Medicines Agency – Luxembourg Agency for Medicines and Health Products
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EU | Revised PASS Guidance
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PERU | New Regulations of the Personal Data Protection Law
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USA | Study of Sex Differences in the Clinical Evaluation of Medical Products
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