Improve your sales and increase customer satisfaction with medical devices that bear the CE Mark, allowing them to be legally sold within the European Union (EU). Get a clear understanding of the European directives to ensure that your products meet designated minimum safety standards and quality levels, while minimizing liability risks associated with noncompliance. Ensure your product can move freely throughout the European Single Market.
Intended for medical device manufacturers who want to export to Europe, this two-day course provides an overview of the following EU directives: Active Implantable Medical Device Directive (AIMDD), Medical Device Directive (MDD), and the In Vitro Diagnostic Device Directive (IVDD). Also covered are the requirements for safety, health, environment, and consumer protection set forth by the European medical device directives.