Whether you're a regional distributor, a global brand looking to license, or another manufacturer seeking sterile fill-finish capacity — we have a structured engagement model for it.
Out-licensing of marketed and approved biosimilars to regional brand owners — with the dossier, support and post-market surveillance to make a launch successful.
Use our WHO-GMP sterile fill-finish capacity for your biologic in vials, pre-filled syringes or cartridges. Combi line ready for fast format changeover.
Partner with our manufacturing and regulatory teams from formulation forward. We bring end-to-end downstream capability; you bring market access, capital or complementary expertise.
Authorized distributors across CIS, LATAM, Africa, SE Asia and the Middle East — with cold-chain logistics, regulatory support and tender desk.
Tell us a bit about your market, model and timeline — our partnerships team responds within two business days.