Канал: Med-Di-Dia

QSR to QMSR - Is ISO 13485 the ultimate champion?

QSR to QMSR - Is ISO 13485 the ultimate champion?

Where are we now EU MDR

Where are we now EU MDR

Regulatory Affairs Support for MedTech

Regulatory Affairs Support for MedTech

Cyber Attack on Digital Health

Cyber Attack on Digital Health

MDD to MDR Transition Timeline

MDD to MDR Transition Timeline

What is a quality management system for Medical Devices?

What is a quality management system for Medical Devices?

Harmonisation and Standardisation for IVD Medical Device

Harmonisation and Standardisation for IVD Medical Device

Med-Di-Dia Turns 3 #MDD3

Med-Di-Dia Turns 3 #MDD3

Up in The World - Med-Di-Dia

Up in The World - Med-Di-Dia

What Are GS1 Standards?

What Are GS1 Standards?

Medical Device Regulations

Medical Device Regulations

IVDR Celebration Week - Closing Ceremony

IVDR Celebration Week - Closing Ceremony

Where to Start in order to launch an IVD Medical Device onto the EU Market

Where to Start in order to launch an IVD Medical Device onto the EU Market

IVDR Celebration Week - What is a clinical performance study, and why do you need it?

IVDR Celebration Week - What is a clinical performance study, and why do you need it?

IVDR Celebration Week - IVD Medical Device - the need for UDI and Barcodes

IVDR Celebration Week - IVD Medical Device - the need for UDI and Barcodes

IVDR Celebration Week - IVDR - Understanding SaMD and Cyber Security Requirements

IVDR Celebration Week - IVDR - Understanding SaMD and Cyber Security Requirements

IVDR Celebration Week - IVDR and the Clinical Requirements for IVD Manufacturers in Europe

IVDR Celebration Week - IVDR and the Clinical Requirements for IVD Manufacturers in Europe

IVDR Celebration Week - Overview of IVDR

IVDR Celebration Week - Overview of IVDR

IVDR Celebration Week - Opening Ceremony

IVDR Celebration Week - Opening Ceremony

IVDR celebration Week

IVDR celebration Week

IVDR MasterClass Med-Di-Di + GRS + EIT Health

IVDR MasterClass Med-Di-Di + GRS + EIT Health

How Regulatory Compliance in Medtech Is a Tool for Success - OnHelix Innovation Workshop

How Regulatory Compliance in Medtech Is a Tool for Success - OnHelix Innovation Workshop

MedTech and the Internet of Medical Things at #GenesisLondon

MedTech and the Internet of Medical Things at #GenesisLondon

8 Challenges of Medical Devices

8 Challenges of Medical Devices

European Union Authorised Representative EU AR

European Union Authorised Representative EU AR

Is your Innovation a Medical Device?

Is your Innovation a Medical Device?

Regulatory Help for Medical Device Start Ups

Regulatory Help for Medical Device Start Ups

Class 3 Medical Device EU MDR

Class 3 Medical Device EU MDR

Class II B medical device EU MDR

Class II B medical device EU MDR

Class II A medical device in EU MDR

Class II A medical device in EU MDR

Greer Deal's Celebration Message on Med-Di-Dia's Second Anniversary

Greer Deal's Celebration Message on Med-Di-Dia's Second Anniversary

Second Anniversary Celebration - Med-Di-Dia Turns 2!

Second Anniversary Celebration - Med-Di-Dia Turns 2!

SaMD - MedTech

SaMD - MedTech

Class 1 Medical Device EU MDR

Class 1 Medical Device EU MDR

Understanding the EU MDR

Understanding the EU MDR

PRRC Roles and Responsibilities

PRRC Roles and Responsibilities

MDD MDR Classes of Medical Device

MDD MDR Classes of Medical Device

Around the World in Medical Technology Regulation

Around the World in Medical Technology Regulation