Serving Customers Across the
Pharma Value Chain
Chieron is a strategic partner for CDMO/CMO opportunities and API/Intermediates for clients across India, Europe, USA, Japan, South Korea, Brazil, China, and the Middle East.
Transparency, Predictability & Supply Security
With a strong foundation built on backward integration, green chemistry, and regulatory compliance, we aspire to achieve a top-three global market position for all our molecules. We emphasize transparency and proactive communication with clients to mitigate global raw material price fluctuations while ensuring uncompromised supply continuity.
Aiming for leadership in all 15–20 commercial APIs through continuous synthesis.
Dedicated Client Segment Teams
Specialized cross-functional experts with over two decades of industry experience across R&D, regulatory affairs, operations, and IT.
Originators & Innovators
Cross-functional team handling early-stage inquiries, technical route design, non-infringing IP pathways, and rapid tech transfer to pilot scale.
Specialty Chemicals
Manages complex chemical requirements and rigorous electronic/semiconductor grade specifications, ensuring seamless execution from lab to plant.
Generic Pharma Leaders
Coordinates tight alignment between manufacturing, regulatory affairs, and inventory planning to deliver commercial APIs with an 8–10 week lead time.
Integrated from Concept to Commercialisation
A seamless, transparent pathway from laboratory synthesis to multi-ton commercial launch.
Route Scouting & R&D
Developing robust, non-infringing synthetic routes with high atom economy and green biocatalysis.
Analytical Method Validation
GLP/GDP compliant ADL methods, genotoxic impurity profiling, and nitrosamine risk assessments.
Kilo Lab & Pilot Scale
100L scale automated GLRs and pilot plant validation batches to establish process control parameters.
Regulatory Filing & Tech Transfer
Complete DMF preparation (US-DMF, CEP, Canada, Australia) and regulatory query resolution.
Commercial Manufacturing
350+ KL plant capacity, 7 ISO-8 cleanrooms, continuous manufacturing, and guaranteed 8–10 week lead time.
Have a New Chemical Entity (NCE) or Custom Synthesis Project?
Collaborate with our 20+ Ph.D. research scientists and experienced techno-legal patent team.