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Personalised maxillofacial bone regeneration


Scientific Advisory Board reports

Four reports will be generated during the project the first one at M12 and then at M24 M36 and M54 due date indicated above

Develop a common clinical protocol for ethical committees and Medicine Agency submission

Includes investigator brochure, patient’s information sheets and consent forms in all languages from the participating centres.

Educational programs associated with universities

Report on educational programs will be delivered at M24 for the first time and then repeated at M36 and M48 the due date indicated above

License for custom made medical device manufacturing

Title is selfdescribing additional details may be provided at request

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