Knowledge Series-What You Need to Know About MDR
Knowledge Series-What You Need to Know About MDR
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Knowledge Series-What You Need to Know About MDR

Knowledge Series-What You Need to Know About MDR

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Medical Device Regulation codes

Medical Device Regulation codes

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The Step-by-step method to get MDR - IVDR Certified

The Step-by-step method to get MDR - IVDR Certified

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What can we learn from 100 days of audits (EU MDR 2017/745)

What can we learn from 100 days of audits (EU MDR 2017/745)

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What can we learn from the first MDR audits with Martin Witte (TÜV SÜD)

What can we learn from the first MDR audits with Martin Witte (TÜV SÜD)

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The best tips to build an MDR / IVDR Project? (Medical Device Regulation)

The best tips to build an MDR / IVDR Project? (Medical Device Regulation)

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What are Cybersecurity requirements under EU MDR?

What are Cybersecurity requirements under EU MDR?

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What are Common Specifications within MDR & IVDR? [Stefan Bolleininger]

What are Common Specifications within MDR & IVDR? [Stefan Bolleininger]

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Pokémon Sleep: Cresselia vs Darkrai Event Day 10 & Analyzing My Team Members

Pokémon Sleep: Cresselia vs Darkrai Event Day 10 & Analyzing My Team Members

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Multidrug-Resistant Tuberculosis (MDR-TB): Mycobacterium tuberculosis

Multidrug-Resistant Tuberculosis (MDR-TB): Mycobacterium tuberculosis

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Medical Device Regulation Transition Timeline (MDR 2017/745)

Medical Device Regulation Transition Timeline (MDR 2017/745)

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UDR, MDR, XDR, and DTR - AMR Slides

UDR, MDR, XDR, and DTR - AMR Slides

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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

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Distributor role within MDR and IVDR with Nicolaj Nitzsch

Distributor role within MDR and IVDR with Nicolaj Nitzsch

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MDR/IVDR — Economic operator obligations, Eudamed and national registration requirements

MDR/IVDR — Economic operator obligations, Eudamed and national registration requirements

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Webinar: Clinical Investigations - Transitioning from MDD to MDR

Webinar: Clinical Investigations - Transitioning from MDD to MDR

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MedTech Intelligence: Now that the EU MDR deadline is passed, how do you sell your device abroad?

MedTech Intelligence: Now that the EU MDR deadline is passed, how do you sell your device abroad?

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What you should know about Vigilance Reporting for Medical Devices?

What you should know about Vigilance Reporting for Medical Devices?

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Tuberculosis - causes, symptoms, diagnosis, treatment, pathology

Tuberculosis - causes, symptoms, diagnosis, treatment, pathology

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Implant Card Requirements for Article 18 of EU MDR

Implant Card Requirements for Article 18 of EU MDR

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