Emergo by UL

1:33

Overcome post-market surveillance challenges with help from Emergo by UL

1:59

Design your products around people, get support to access global markets faster

2:22

Use RAMS to power your medical device regulatory activities worldwide

1:29:08

Medical Device Regulatory Market Access in Times of a National Emergency

2:52

Explore medical device and IVD market access

3:57

Discover Human Factors Research & Design at Emergo by UL

1:45

Discover RAMS - medical device regulatory intelligence software

Emergo by UL Live Stream

4:52

Introduction to the UDI System in the USA

10:44

Introduction to Medical Device Labeling Symbols

6:41

What To Expect From Your Regulatory Representative

4:18

How to Prepare for an FDA Inspection

6:50

Overview of the USA FDA Classification Process

4:34

Introduction to Clinical Evaluation Reports (CER) for Europe

4:13

Malaysia 2015 Overview HB

3:57

United States Medical Device Registration Chapter 2 - Classification

3:25

United States Medical Device Registration Chapter 3 - Quality Management System

3:59

United States Medical Device Registration Chapter 1 - Overview

3:09

United States Medical Device Registration Chapter 4 - Product Testing

2:40

United States Medical Device Registration Chapter 7 - Device Listing

2:08

United States Medical Device Registration Chapter 6 - Representation

5:13

United States Medical Device Registration Chapter 5 - Dossier Preparation

2:59

South Korea Medical Device Registration Chapter 5 - Registration

2:57

South Korea Medical Device Registration Chapter 6 - Final Steps

2:11

South Korea Medical Device Registration Chapter 2 - Classification

2:11

South Korea Medical Device Registration Chapter 1 - Overview

3:01

South Korea Medical Device Registration Chapter 4 - Quality Management System

1:32

South Korea Medical Device Registration Chapter 3 - Key Players

2:53

Mexico Medical Device Registration Chapter 1 - Overview

5:20

Mexico Medical Device Registration Chapter 4 - Registration Routes

2:04

Mexico Medical Device Registration Chapter 3 - Key Players

2:38

Mexico Medical Device Registration Chapter 5 - Post-market

2:39

Mexico Medical Device Registration Chapter 2 - Classification

2:15

Japan Medical Device Registration Chapter 6 - Final steps

2:33

Japan Medical Device Registration Chapter 5 - Applications

2:32

Japan Medical Device Registration Chapter 4 - Quality Management System

3:11

Japan Medical Device Registration Chapter 3 - Key Players

3:35

Japan Medical Device Registration Chapter 1 - Overview

3:25

Japan Medical Device Registration Chapter 2 - Classification

2:59

European Medical Device Registration Chapter 5 - Key Players

4:41

European Medical Device Registration Chapter 1 - Overview

3:11

European Medical Device Registration Chapter 6 - Final Steps

3:37

European Medical Device Registration Chapter 2 - Classification

4:18

European Medical Device Registration Chapter 4 - Technical File

2:19

European Medical Device Registration Chapter 3 - Quality Management System

1:50

Brazil Medical Device Registration Process Chapter 3 - Registration Holder

3:20

Brazil Medical Device Registration Process Chapter 6 - Registration

2:53

Brazil Medical Device Registration Process Chapter 4 - Quality Management System

3:06

Brazil Medical Device Registration Process Chapter 5 - Technical File

3:10

Brazil Medical Device Registration Process Chapter 1 - Overview

3:29

Brazil Medical Device Registration Process Chapter 2 - Classification

3:54

Overview of the Medical Device Market in Mexico

4:53

Overview of the Medical Device Market in Japan

4:23

European Medical Device Market Overview

4:11

Brazil Medical Device Registration Overview