We are a CDMO specialized in nanotechnologies, particle engineering, and bioprocessing, supporting drug development from early-phase formulation through GMP manufacturing.

Our services include drug product formulation, process and analytical development, and GMP production for oral, injectable, and topical dosage forms, covering technology transfer, scale-up, and batch release.

We support customers worldwide with aseptic fill & finish and lyophilization services providing tailor-made solutions for clinical trial programs, personalized medicines, and commercial products.

Our GMP-certified manufacturing facility (500 m²) features EU GMP Annex 1–compliant cleanrooms from Grade D to Grade A, enabling flexible and compliant production. Our capabilities cover a broad range of compounds, including small molecules, biologics (peptides, proteins, monoclonal antibodies), and advanced nanoparticle formulations.