Work package number 5 Lead beneficiary MMATECH
Work package title                   Certification and regulatory issues 
Participant number 1
Short name of participant MMATECH
Person/months per participant: 10
Start month M7 End month M24
O5.1 To apply for the CE mark for MP-ORIF.
D5.1 (M24) CE mark for medical device certification dossier. The dossier will guarantee that MP-ORIF meets the EU safety, health and environment requirements and is in compliance with EU regulations.