MDRG 15/04/2024 MDRG 15/04/2024 Medical Device Lifetime Overview Read More MDRG 12/04/2024 MDRG 12/04/2024 IVDR Implementation Plan Summary Read More MDRG 10/04/2024 MDRG 10/04/2024 Navigating Language Requirements for Medical Device Manufacturers Read More MDRG 08/04/2024 MDRG 08/04/2024 Enhanced Vigilance Reporting Guidelines for Breast Implants: MDCG 2024-1-4 Overview Read More MDRG 05/04/2024 MDRG 05/04/2024 Guidance for Reporting Incidents with Cardiac Implantable Electronic Devices (CIEDs) Read More MDRG 03/04/2024 MDRG 03/04/2024 Guidance for Vigilance Reporting on Coronary Stents and Delivery Systems Read More MDRG 01/04/2024 MDRG 01/04/2024 Guidance on Vigilance for Cardiac Ablation Devices: Key Insights Read More MDRG 29/03/2024 MDRG 29/03/2024 Guidance on Vigilance Reporting for CE-Marked Devices: An Overview Read More MDRG 27/03/2024 MDRG 27/03/2024 EUDAMED Update v2.14.0 Highlights Read More MDRG 25/03/2024 MDRG 25/03/2024 Clarifying "Significant Change" in Medical Devices: Health Canada's Updated Guidance Read More MDRG 22/03/2024 MDRG 22/03/2024 Streamlining European Medical Device Nomenclature: MDCG 2024-2 Read More MDRG 20/03/2024 MDRG 20/03/2024 MDCG 2024-3: A New Benchmark for Clinical Investigation Plans Read More MDRG 19/03/2024 MDRG 19/03/2024 Insights from the 6th Notified Bodies Survey on MDR/IVDR Certifications and Applications Read More MDRG 18/03/2024 MDRG 18/03/2024 EU Artificial Intelligence Act Adopted Read More MDRG 04/12/2023 MDRG 04/12/2023 MDSAP Quality Management System Manual Updated (6th Edition) Read More MDRG 01/12/2023 MDRG 01/12/2023 New IVDR Notified Body – Sertio Oy Read More MDRG 30/11/2023 MDRG 30/11/2023 Congratulations to Notice Belgelendirme, Muayene ve Denetim Hizmetleri Anonim Şirketi on their recent notification as a Notified Body under the MDR! Read More MDRG 29/11/2023 MDRG 29/11/2023 Read More MDRG 27/11/2023 MDRG 27/11/2023 New MDCG 2023-4: MDSW Read More MDRG 25/11/2023 MDRG 25/11/2023 Black Friday Sale Now On! Read More Older Posts
MDRG 10/04/2024 MDRG 10/04/2024 Navigating Language Requirements for Medical Device Manufacturers Read More
MDRG 08/04/2024 MDRG 08/04/2024 Enhanced Vigilance Reporting Guidelines for Breast Implants: MDCG 2024-1-4 Overview Read More
MDRG 05/04/2024 MDRG 05/04/2024 Guidance for Reporting Incidents with Cardiac Implantable Electronic Devices (CIEDs) Read More
MDRG 03/04/2024 MDRG 03/04/2024 Guidance for Vigilance Reporting on Coronary Stents and Delivery Systems Read More
MDRG 01/04/2024 MDRG 01/04/2024 Guidance on Vigilance for Cardiac Ablation Devices: Key Insights Read More
MDRG 29/03/2024 MDRG 29/03/2024 Guidance on Vigilance Reporting for CE-Marked Devices: An Overview Read More
MDRG 25/03/2024 MDRG 25/03/2024 Clarifying "Significant Change" in Medical Devices: Health Canada's Updated Guidance Read More
MDRG 22/03/2024 MDRG 22/03/2024 Streamlining European Medical Device Nomenclature: MDCG 2024-2 Read More
MDRG 20/03/2024 MDRG 20/03/2024 MDCG 2024-3: A New Benchmark for Clinical Investigation Plans Read More
MDRG 19/03/2024 MDRG 19/03/2024 Insights from the 6th Notified Bodies Survey on MDR/IVDR Certifications and Applications Read More
MDRG 04/12/2023 MDRG 04/12/2023 MDSAP Quality Management System Manual Updated (6th Edition) Read More
MDRG 30/11/2023 MDRG 30/11/2023 Congratulations to Notice Belgelendirme, Muayene ve Denetim Hizmetleri Anonim Şirketi on their recent notification as a Notified Body under the MDR! Read More
