[March 06, 2018]

Three Day Seminar: An Introduction to the Medical Device Regulation (London, United Kingdom - November 12-14, 2018) - ResearchAndMarkets.com

The "An Introduction to the Medical Device Regulation" conference has been added to ResearchAndMarkets.com's offering.

Gain a comprehensive understanding of the regulatory requirements

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.

This is an excellent introduction from leading experts in the field and delegates should expect three comprehensive days of training.

Why you should attend

BENEFITS OF ATTENDING

This seminar provides a detailed introduction to the European medical device legislation. It will explain the new regulations 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. This is an excellent introduction from leading experts in the field and delegates should expect three comprehensive days of training.

• 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 (News - Alert)
• Plan your Clinical Evaluations

For more information about this conference visit https://www.researchandmarkets.com/research/2b9hl8/an_introduction?w=4

View source version on businesswire.com: http://www.businesswire.com/news/home/20180306006523/en/

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