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mdcg mdr change

MDR vs MDD : 13 Key Changes

MDR vs MDD : 13 Key Changes


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

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


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

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


BSI Compliance Navigator | MDR and IVDR – Key changes

BSI Compliance Navigator | MDR and IVDR – Key changes


Medical Device Regulation codes

Medical Device Regulation codes


The 5 most relevant changes the Medical Device Regulation MDR introduces, that  you must know

The 5 most relevant changes the Medical Device Regulation MDR introduces, that you must know


MDCG issued  guidance for classifying medical devices

MDCG issued guidance for classifying medical devices


What is a Significant Change for your Medical Devices?

What is a Significant Change for your Medical Devices?


MDD to MDR Transition Timeline

MDD to MDR Transition Timeline



Maven Masterclass: Training on Key Changes: EU MDD to EU MDR

Maven Masterclass: Training on Key Changes: EU MDD to 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


BSI Compliance Navigator | MDCG documents

BSI Compliance Navigator | MDCG documents


EU MDR and IVDR consolidated versions

EU MDR and IVDR consolidated versions


Medical Device Directive (MDD) to Medical Device Regulation (MDR)

Medical Device Directive (MDD) to Medical Device Regulation (MDR)


Hear about the changes to the  EU MDR and IVDR and the future of the medical device industry

Hear about the changes to the EU MDR and IVDR and the future of the medical device industry


MDCG 2022-11 Rev 1 Position Pape

MDCG 2022-11 Rev 1 Position Pape


When should you apply the MDR in Europe ? [Medical Device Regulation]

When should you apply the MDR in Europe ? [Medical Device Regulation]


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