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

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


Medical Device Regulation codes

Medical Device Regulation codes


MDR vs MDD : 13 Key Changes

MDR vs MDD : 13 Key Changes


MDCG issued  guidance for classifying medical devices

MDCG issued guidance for classifying medical devices


TÜV SÜD MDR Interpretation: MDCG 2019-14

TÜV SÜD MDR Interpretation: MDCG 2019-14


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

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


What is the EU Medical Devices Regulation (MDR)?

What is the EU Medical Devices Regulation (MDR)?


MDCG 2021-27 - Placing on the market & relabelling with Erik Vollebregt

MDCG 2021-27 - Placing on the market & relabelling with Erik Vollebregt


MDCG Class 1 Guidance

MDCG Class 1 Guidance



Introduction to the European Medical Devices Regulation   MDR EU 2017 745

Introduction to the European Medical Devices Regulation MDR EU 2017 745


MDCG 2022-11 Rev 1 Position Pape

MDCG 2022-11 Rev 1 Position Pape


Understanding Key Components of a Medical Device Clinical Evaluation

Understanding Key Components of a Medical Device Clinical Evaluation


What Is a Medical Device? (New Medical Device Regulation MDR 2017/745)

What Is a Medical Device? (New Medical Device Regulation MDR 2017/745)


MDR KILAVUZ BELGELER - MDR GUIDANCE DOCUMENTS- 23.12.2022

MDR KILAVUZ BELGELER - MDR GUIDANCE DOCUMENTS- 23.12.2022


Software as a Medical Device Classification Rule 11 (EU MDR 2017/745)

Software as a Medical Device Classification Rule 11 (EU MDR 2017/745)


Classification Medical Device in EU (Medical Device Regulation MDR 2017/745)

Classification Medical Device in EU (Medical Device Regulation MDR 2017/745)


Vigilance MD PSURs for Medical Device

Vigilance MD PSURs for Medical Device


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

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