15th-17th May 2018 | Amsterdam, the Netherlands

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Comparative Perspectives on MDR Preparations

Pharma IQ spoke exclusively with two industry experts from Siemens Healthineers and Bactiguard on the upcoming MDR and the impact that they see this having both within their organisations and in the broader medical device industry.

Have you developed your strategy to address the new EU MD and IVD Regulations? 

This article discusses the new EU Medical Device and InVitro Device Regulations. Approved by the European Parliament in May 2017, these new regulations are the biggest change to the legislative framework for MD and IVD products in decades.Companies will need to implement many new or enhanced capabilities to meet these obligations.