An Introduction to the Medical Device Regulation is organized by Management Forum (Mf) Ltd and will be held during May 14 - 16, 2018 at The Cavendish Hotel, London, England, United Kingdom. The target audience for this medical event is Pharmacovigilance, Regulatory Affairs, Quality Assurance, Technical Support and 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.
Course Overview:
This seminar provides a detailed introduction to the European medical device legislation. It will explain the Regulation and which products are covered, the involvement of Notified Bodies, how to choose one and outline what a manufacturer must do.
Conference Objectives are :
• 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.