21 June 2022

Transforming scientific innovations into a marketable product is always a challenging path. Walking down this exciting avenue, regulation plays a fundamental role to guarantee quality and sustainability, but can also bring about uncertainties which need to be faced up early in the process.

That is why GIOTTO took part to the “Regulatory seminar on advanced additive manufacturing solutions for healthcare applications”, co-organized with EU-funded projects ADMAIORA, BRAVE, INKPLANK, ISMARD and TRIANKLE.

Expert speakers from industry and regulatory have presented and opened up discussions with the consortia about the regultory landscape, as well as regulatory experiences on Advanced Therapy Medicinal Products (ATPMs) in the EU, quality requirements and practical examples of certification and clinical development of combined ATMPs.

The seminar has been provide precious insights to ensure success of all participating projects!

Stay tuned for next updates from GIOTTO