An Introduction to the Medical Devices Directives is organized by Management Forum Ltd and would be held during Nov 20 - 22, 2017 at The Rembrandt Hotel, London, England, United Kingdom.
The target audience for this medical event for Past delegates include personnel from the following departments: regulatory affairs, pharmacovigilance, quality assurance and technical support. This seminar will be of interest to all personnel who are new to the medical device industry, all those who intend to place a medical device on the market and anyone who requires an overview of the medical device sector.
This seminar provides a detailed introduction to the European medical device legislation. It will explain the Directives and which products are covered, the involvement of Notified Bodies, how to choose one and outline what a manufacturer must do. It will also cover the documentation necessary to apply for the CE Mark.
Benefits Of Attending :
• Learn the role of a Notified Body
• Know what a Competent Authority expects
• Better under Conformity Assessment Procedures, Classification, Medical Device legislation
• Comply with Manufacturing Responsibilities
• Consider the requirements for Quality Systems
• Plan your Clinical Evaluations
Additional details will be posted as soon as they are available.