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Hear about the latest update on the EU Medical Device Regulation and share your thoughts and questions with your peers and industry experts

New EU Regulations for medical devices and in vitro diagnostics which will provide enhanced protection for patients and users has now been published in the Official Journal of the European Union. The new regulations, which have been in development since 2012, will come into effect at the end of May.

With these new regulations in mind, Codico invites you to our webinar featuring a panel of subject matter experts. During this free exclusive webinar, various subjects and themes will be discussed. In particular, the EU Legislative requirements and what this means for your manufacturing processes and overall business. It will feature a specific case study – “UDI on pens”. Furthermore, we will investigate and debate the data management and reporting aspects of unique device identification.

During this free webinar you will learn:

1. EU Legislative requirements
2. Case Study: UDI on pens
3. Data management and reporting

Date: Thursday, June 01 at 2PM.

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