• 21/01/2026 22:07

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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

Canada – Regulations Amending the Medical Devices Regulations (Establishment Licenses)

Canada - Regulations Amending the Medical Devices Regulations (Establishment Licenses)

Japan – Partial Amendment to the Criteria for Vascular Prosthesis and the Criteria for Medical Adhesive, and Abolishment of the Criteria for Vision Corrective Contact Lens

Japan - Partial Amendment to the Criteria for Vascular Prosthesis and the Criteria for Medical Adhesive, and Abolishment of the Criteria for Vision Corrective Contact Lens

South Korea – Partial Amendment to the «Regulations on Medical Device Manufacturing and Quality Management»

South Korea - Partial Amendment to the "Regulations on Medical Device Manufacturing and Quality Management"

South Korea – Proposed Amendment to the “Regulations on the Classification Categories of Digital Medical Products”

South Korea - Proposed Amendment to the “Regulations on the Classification Categories of Digital Medical Products”

South Korea – Proposed Amendments to the “Regulations on In Vitro Diagnostic Medical Device Group and Class by Group”

South Korea - Proposed Amendments to the “Regulations on In Vitro Diagnostic Medical Device Group and Class by Group”