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