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mdcg medical device coordination group

Understanding the MDCG 2021-24: Navigating the Complex World of Medical Device Classification

Understanding the MDCG 2021-24: Navigating the Complex World of Medical Device Classification


MDCG issued  guidance for classifying medical devices

MDCG issued guidance for classifying medical devices


Medical Device Regulation

Medical Device Regulation


Short course on the Medical Device Regulation (EU) 2017/745

Short course on the Medical Device Regulation (EU) 2017/745


Understanding Key Components of a Medical Device Clinical Evaluation

Understanding Key Components of a Medical Device Clinical Evaluation


Webinar | Safer medical devices: Implementation of the EU MDR and EUDAMED database

Webinar | Safer medical devices: Implementation of the EU MDR and EUDAMED database


The Road to Market Authorization for Sterile Medical Devices within the EU

The Road to Market Authorization for Sterile Medical Devices within the EU


Medical Device Regulation codes

Medical Device Regulation codes



TÜV SÜD: The new IVDR Classification guidance MDCG 2020-16

TÜV SÜD: The new IVDR Classification guidance MDCG 2020-16


How to CE mark an Accessory for a Medical Device?

How to CE mark an Accessory for a Medical Device?


Information and updates regarding the EU MDR implementation

Information and updates regarding the EU MDR implementation


How to deal with Significant Changes for your Medical Devices (EU MDR)

How to deal with Significant Changes for your Medical Devices (EU MDR)


Clinical/Performance evaluation for Medical Device Software (MDR IVDR)

Clinical/Performance evaluation for Medical Device Software (MDR IVDR)


The European Medical Device New Regulation 2017/745

The European Medical Device New Regulation 2017/745


MDR/IVDR: Sufficient clinical data, equivalency for legacy devices and the CIE 2021 work programme

MDR/IVDR: Sufficient clinical data, equivalency for legacy devices and the CIE 2021 work programme


MDR and IVDR update: Overview and status of EU and national implementation

MDR and IVDR update: Overview and status of EU and national implementation


Introduction to the European Medical Devices Regulation   MDR EU 2017 745

Introduction to the European Medical Devices Regulation MDR EU 2017 745


MDR KILAVUZ BELGELER - MDR GUIDANCE DOCUMENTS- 23.12.2022

MDR KILAVUZ BELGELER - MDR GUIDANCE DOCUMENTS- 23.12.2022


Vigilance MD PSURs for Medical Device

Vigilance MD PSURs for Medical Device