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MB Therapeutics cleared to manufacture cartridges for 3D printed drugs

MB Therapeutics announces ANSM authorization for a pharmaceutical establishment making cartridges intended for 3D printed medicines.

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MB Therapeutics founders Ian Soulairol & Stéphane Roulon

In a statement dated September 30, 2026, French company MB Therapeutics says it has received authorization from the French National Agency for the Safety of Medicines and Health Products (ANSM) to open a pharmaceutical establishment manufacturing a semi-solid intermediate in cartridges for 3D printing solid oral dosage forms.

The company describes this authorization as a world first for these cartridges under pharmaceutical manufacturer status. This differs from the Finnish company CurifyLabs, which already offers excipient bases that it says are manufactured under Good Manufacturing Practices (GMP), and which pharmacists combine with the active ingredient. The two announcements concern different intermediate products.

Standardizing the cartridge to personalize the dose

Standardized doses may not meet the needs of some patients, including children or elderly people who require tailored doses or oral forms that are easier to take. In the approach described by MB Therapeutics, a patented cartridge is intended to be the standardized pharmaceutical product, manufactured under Good Manufacturing Practices.

Personalization is then planned at the point of care: the company’s 3D printers, designed for hospital pharmacies, would use these cartridges to produce oral forms with a dose adapted to each patient. The company presents the model as a way to ensure quality and traceability from cartridge production through to printing.

In its communication accompanying the announcement, MB Therapeutics describes the authorization as paving the way for the future opening of its establishment. It does not describe an already operational site.

“Beyond precise dose adjustment and rapid availability in the pharmacy, 3D printing makes it possible to offer adapted dosage forms, such as personalized dispersible and orodispersible forms,” says Dr Manon Perez, pharmacist and Quality Director at MB Therapeutics.
That said, regulatory clearance is one hurdle while market access is another one. As we explored in our dossier on reimbursement pathways for 3D printing in Europe, the technology is often ready before the system is.

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