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  • EU – Guidance on Post-Market Surveillance of Medical Devices and In Vitro Diagnostic Medical Devices

EU – Guidance on Post-Market Surveillance of Medical Devices and In Vitro Diagnostic Medical Devices

EU - Guidance on Post-Market Surveillance of Medical Devices and In Vitro Diagnostic Medical Devices

UK – The Medical Devices (Post-Market Surveillance Requirements) (Amendment) (Great Britain) Regulations 2024

UK - The Medical Devices (Post-Market Surveillance Requirements) (Amendment) (Great Britain) Regulations 2024