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mdcg guidance legacy devices ivdr

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

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


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


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


IVDR update: IVD classification rules and performance evaluation

IVDR update: IVD classification rules and performance evaluation


Navigating the In Vitro Diagnostic Regulation (IVDR) Rollout for Legacy & New Devices - Webinar

Navigating the In Vitro Diagnostic Regulation (IVDR) Rollout for Legacy & New Devices - Webinar


Everything you need to know about the IVDR

Everything you need to know about the IVDR


TÜV SÜD IVDR Interpretation | Marta Carnielli | Introduction to guidance MDCG2020-16

TÜV SÜD IVDR Interpretation | Marta Carnielli | Introduction to guidance MDCG2020-16


MDCG issued  guidance for classifying medical devices

MDCG issued guidance for classifying medical devices


Understanding the IN VITRO DIAGNOSTIC REGULATION (IVDR) Everything You Need to Know

Understanding the IN VITRO DIAGNOSTIC REGULATION (IVDR) Everything You Need to Know


MDR vs MDD : 13 Key Changes

MDR vs MDD : 13 Key Changes


IVDR tutorial for diagnostic labs 7: Guidance, concerns, recommendations

IVDR tutorial for diagnostic labs 7: Guidance, concerns, recommendations


MDCG Releases Two Guidance Documents

MDCG Releases Two Guidance Documents


How to write your Performance Evaluation [IVDR 2017/746]

How to write your Performance Evaluation [IVDR 2017/746]


Critical Concepts: Deep Dive into MDR and IVDR Device Classification and Data Collection Strategies

Critical Concepts: Deep Dive into MDR and IVDR Device Classification and Data Collection Strategies



Ask the Expert: A Deep Dive into MDR and IVDR Device Classification and Data Collection Strategies

Ask the Expert: A Deep Dive into MDR and IVDR Device Classification and Data Collection Strategies


Changing Requirements for Manufacturers Under IVDR

Changing Requirements for Manufacturers Under IVDR


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

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


What was the MDCG 2023-4 guidance for and why this came out ?

What was the MDCG 2023-4 guidance for and why this came out ?