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

(14:55)

Introduction to the European Medical Devices Regulation MDR EU 2017 745

(32:47)

What Is a Medical Device? (New Medical Device Regulation MDR 2017/745)

(15:58)

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

(8:23)

What is Post Marketing Surveillance for Medical Devices? (MDR 2017/745)

(39:56)

Medical Device Regulation Transition Timeline (MDR 2017/745)

(10:53)

How to make labelling regulatory compliant for EU-MDR (2017/745)

(34:22)

Medical Device Rules, 2017: Implications on medical devices

(1:20:46)

Bloopers: Recording Introduction to the Medical Device Regulation (EU) 2017/745

(39)

How much does Cost the new Medical Device Regulation [2017/745]

(25:51)

The ABCs of Medical Device Software Compliance under EU Regulations 2017/745 and 2017/746 - Webinar

(1:1:39)

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

(38:8)

How to market a custom-made medical device? (EU MDR 2017/745)

(7:22)

How to choose your PRRC ? (EU MDR 2017/745 - IVDR 2017/746)

(48:15)

How to evaluate your Medical Device in 3 Steps (EU MDR 2017/745)

(38:45)

What is European Medical Device Regulation (EU MDR)?

(7:21)

Is my Software a Class I Medical device? [EU MDR 2017/745]

(1:5:21)

The new EU Medical Device Regulation EU MDR 2017/745 with Monir El Azzouzi

(28:53)