Accelerate Innovation.
Advance Your Molecule
with Confidence.
Discovery. Development. Manufacturing.
One Trusted CRDMO Partner
Commercialized
Book a meeting at CPHI
What thirty minutes at our stand actually gets you
Accelerate Development Timelines
Usually: Six weeks after the show you are still waiting on a feasibility view, and the programme has not moved.
With Aurigene: Accelerated IND-enabling timelines of 6-12 months for complex small molecules and 9 months for biologics.
Integrated Development & Manufacturing
Usually: Drug substance and drug product sit with different suppliers - managing the seam between them becomes your job, not theirs.
With Aurigene: One integrated global partner from discovery to commercial manufacturing, across 16 USFDA sites, eliminating handoff risks.
Single Quality System
Usually: Each supplier runs its own QMS - reconciling them and scheduling audits is your overhead, not theirs.
With Aurigene: Our Quality-First approach ensures patient safety and data integrity remain uncompromised.
Peptide Expertise
Usually: Most CDMOs top out at gram scale for complex peptides - commercial volume means switching supplier and revalidating.
With Aurigene: Peptides & Fragments synthesized via SPPS/ LPPS/ TAPS from milligram to commercial tonnage.
Clinical-to-Commercial Scale-Up
Usually: Capacity is "available" right up until you ask for a firm date against your timeline.
With Aurigene: 4,100 m³ across 1, 250 reactors; 2,100 MT API per year; 20 KL biologics DS across sites from India, UK and Mexico.
Discovery to commercial supply, under one roof
Small Molecule CRDMO
Route scouting and process development through GMP API and commercial supply, including potent and high-containment work.
Peptide Development & Manufacturing
Solid-phase and solution-phase peptide synthesis, scaled to commercial volumes - capacity most mid-tier CDMOs cannot offer.
Biologics CRDMO
Antibody discovery, cell line development, upstream and downstream processing, GMP drug substance and fill finish across four modalities.
Integrated Development Support
Discovery chemistry and biology at one end, GLP toxicology, CMC regulatory and lifecycle support at the other - the parts most CDMOs make you source separately.
Meet the leaders
Pick a day, we will bring the right person
Questions we get asked at the stand
See you at Booth No. 5D18
CPHI Milan, 06-08 October 2026.