With the implementation dates for the new EU Medical Device Regulation (MDR) and in-Vitro Diagnostic Devices (IVD) coming up, Medilink are hosting a regulatory event to provide information on the requirements on the new directives. Hannah Thomas, our Operations Manager, will present on ‘Technical evidence and its role in supporting regulatory compliance’.

About the Regulatory Event

Medilink’s unique event will provide in depth information and practical case studies on the requirements of the new medical device and IVD directives, and on FDA and MDSAP. The event will provide an opportunity for industry representatives, such as CEO’s and regulatory staff involved in decision-making, to have their say on the regulatory issues they face.

The aim of the event is to allow life science companies to learn from each other by sharing experiences and knowledge they have gained in the practical implementation of global medical device and IVD regulations.

Please visit our website to find out more about the new EU Medical Device Regulations.

To find out more about Medilink’s regulatory event, please visit their website.

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