An Introduction to the Medical Devices Directive 2015

An Introduction to the Medical Devices Directive 2015 provides a detailed introduction to the European medical device legislation.

Topics

• Know what a Competent Authority expects
• Learn the role of a Notified Body
• Comply with Manufacturing Responsibilities
• Better under Conformity Assessment Procedures, Classification, Medical Device legislation
• Plan your Clinical Evaltuions
• Consider the requirements for Quality Systems

Who should Attend

• Pharmacovigilance
• Regulatory Affairs
• Technical Support
• Quality Assurance