The correct function of a medical device depends on every single part. Thus, it is all the more important that all parts fulfill the highest safety requirements, because counterfeit products or production faults put the health of the patient at risk. At COMPAMED 2018, you can find numerous solutions that make both production and the supply chain safe.
The MEDICA TECH FORUM in Hall 12 will be held for the nineth time this year. With alternating focal points experts will present technical, scientific, regulatory and political – in any case market-relevant – topics pertaining to the medical technology industry. The leading content-related industry associations SPECTARIS and ZVEI will discuss the German and the international market environment in the most varying ways as well as the implementation of modern processes and methods in practice.
Wednesday, 14 November 2018:
01:00-01:30 p.m.: Medical Device Regulation (MDR) – an introduction [English], Oliver Bisazza, Director Regulations & Industrial Policy, MedTech Europe, Brussels / Belgium
Design, research, development – the way to the finished medical device is long. At the same time, each development step requires different knowledge and skills. At COMPAMED you will find a large number of expert service providers who will be on hand to provide you with advice and support.