EUDAMED Work­shop – Prepar­ing for Compliance

The Euro­pean Com­mis­sion orga­nizes a work­shop on EUDAMED on May 21: Inter­est­ed par­ties may join the event in Stuttgart to gain insights into the manda­to­ry use of EUDAMED under the EU MDR and IVDR. The hybrid event will pro­vide prac­ti­cal guid­ance on UDI reg­is­tra­tion, mar­ket sur­veil­lance, and com­pli­ance require­ments.

As per the orga­niz­ers, eco­nom­ic oper­a­tors, noti­fied bod­ies, and nation­al author­i­ties will ben­e­fit from expert dis­cus­sions on inte­grat­ing EUDAMED into reg­u­la­to­ry processes.

Reg­is­ter by May 5 (phys­i­cal) or May 12 (online) to secure your spot!

Learn more and sign up here.

Source: Euro­pean Commission 

Accom­pa­ny­ing this sub­ject we rec­om­mend the fol­low­ing con­tent on our website

• Q&A doc­u­ment on the grad­ual roll­out of EUDAMED available
• Reg­is­ter­ing a lega­cy device in Eudamed is a good step
• MDCG guid­ance on admin­is­tra­tive prac­tices and tech­ni­cal alter­na­tives until EUDAMED full functionality