Description:
Designed to introduce participants to the CE Marking process and the EU Directives. This course provides an overview of the requirements of the standard, including required documentation and processes.

Background & Concepts

• What does the CE Mark mean?
• What is the origin of the EU Directives?
• The third-party audit concept
• Process Approach to a Quality Management System

Understanding the Requirements

• The requirements and sections of the EU Directive(s) affecting your product
• How to address those requirements at your organization
• How to document the requirements

Notified Bodies and Testing Laboratories

• How to choose a Notified Body
• The costs associated with testing and certification
• Time and resource allocation
• Next steps

Who Should Attend?
Executive officers of your organization, managers, process owners, supervisors, and quality assurance personnel who want to understand the requirements of the EU Directives, what is needed to comply with those requirements, and how to prepare for product testing and certification.

Prerequisites:
No prior knowledge of the EU Directives or CE Marking is required.

Duration: 4 - 6 hours

Type: On-Site Training

Price: $2500 (for up to 15 people)