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Getting ready for EU MDR

​October 2 | Webinar

The EU Medical Device Regulation (MDR – 2017/745) entered into force in May 2017 and will reach its full implementation in May 2020. 

MDR requires all companies that market devices in the EU must ensure not only compliance, but also an efficient implementation of internal adequate processes, technology and documentation according to the regulation.

The first important step to compliance is  to identify your process and technology gaps, conduct a risk assessment and clarify new necessary documentation.

With NNIT’s deep roots in the Life Sciences domain and vast experience with assisting our clients in their journey to compliance, we have the foundation to help you in your adoption of MDR. NNIT has also developed an EU MDR Assessment Tool, which helps you discover all new relevant MDR initiatives (2017/745) for your organization and thereby avoid redundant work and costs as well as delayed compliance.

Join this webinar to learn more about MDR and the steps to compliance.

Agenda:

- EU MDR - Obstacles and New Requirements

- Approach to Compliance - NNIT's Framework

- EU MDR Readiness Assessment Tool - Demo

- How to Form and Execute your EU MDR Project

- Questions

Speakers: Martin Rother Breyen, Senior Business Consultant, NNIT and Bjarne Wiboe, Subject Matter Expert, NNIT

Time and Date: 3 PM CEST / 3 AM ET, Tuesday October 2, 2018

Click here to sign up


 

 

Nicoline Liu Poulsen+45 3077 8562nlpo@nnit.comMarketing Consultanthttp://www.linkedin.com/in/nicoline-liu-poulsenNicoline Liu Poulsen

 

 

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