Medical Device Directive

The UK vs the EU Medical Device Regulations - What are the key differences?

Patient Guard Limited

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

Operon Strategist

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

Medical Device HQ

MDR Effects on Medical Device Processing

Changes to the Medical Devices Directives

TÜV SÜD Product Service UK

What is a medical device?

Medical Device HQ

What is the EU Medical Devices Regulation (MDR)?

GreenSoft Technology, Inc.

Medical Device Directive (MDD) Webinar | Recorded by BES Chairman Dirk ter Haar

BES Healthcare Ltd

Transitioning from the Medical Device Directives (MDD) to the Medical Device Regulation (MDR)

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

Easy Medical Device

European Medical Device Registration Chapter 1 - Overview

Changes in Europe’s Medical Device Regulations: Consequences for Manufacturers

Eurofins Medical Device Testing

European Medical Device Registration Chapter 3 - Quality Management System

Medical Device Regulation Transition Timeline (MDR 2017/745)

Easy Medical Device

The Recast of the Medical Device Directive in Europe

MDR & IVDR

Industry Learnings

Reclassification of Medical Devices, upcoming revisions of EU regulations

GMED North America

How to classify a Medical Device? (EU MDR Case Studies)

Easy Medical Device

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

Easy Medical Device

EMC for Medical Devices Directive (MDD)

Croydon EMC Solutions