Airis serves as the R&D execution partner for leading BioPharma developers — running complex generic programs end-to-end, from molecule selection through regulator-cleared dossier. The relationships are long-running, the work is repeat business, and the dossiers stand up to USFDA, MHRA, and Health Canada review.
Aurobindo
Hetero Labs
Biocon
MSN Labs
Acme Generics
Belcher Pharma Across the last several years, Airis has served as the formulation and analytical R&D backbone for some of the most respected names in generic pharmaceuticals. We don't position ourselves as a vendor — we operate as the embedded R&D function for partners who choose to outsource the hardest part of their pipeline to a team that owns the science end-to-end.
These are co-development relationships, not transactional ones. Our partners come back program after program because the work is delivered cleanly: methods that hold up at validation, BE strategies that hold up in front of FDA, and dossiers that don't bounce.
Co-development is a long game. The partners who choose Airis stay because the work compounds — methods, analytical platforms, and franchise learnings travel with the relationship across every subsequent program.
From molecule selection and IP positioning through API sourcing, formulation, analytical method science, and dossier filing — one team, one accountable thread. Partners don't manage hand-offs.
Deep operational experience filing into USFDA, MHRA, Health Canada, and emerging markets — with a track record of regulator-quiet approvals on the first review cycle. Our partners' dossiers hold up under scrutiny.
Methods, platforms, and learnings travel with the partner across their portfolio. The first program is execution; every program after is leveraged from accumulated franchise knowledge.
In parallel with our partner programs, Airis is actively originating a pipeline of high-barrier complex generics for licensure to dossier developers and B2B platforms. Co-development partners get the embedded R&D function. License partners get a finished, regulator-ready dossier with a pre-qualified manufacturing path attached.