3-hr Virtual Seminar: Medical Device Regulations and Law in the US, EU and Canada

7 February 2012, Palo Alto, United States

Introduction

This 3-hr training will discuss medical device regulations and law in the US, Europe and Canada. It is designed to help the audience with their global compliance and regulatory intelligence, which is necessary to streamline the regulatory process in an organization to achieve sustainability and to remain sustainable and competitive in global markets.