cGMP MANUFACTURING
Manufacturing APIs & Intermediates
High-capacity chemical synthesis and API production facilities equipped with glass-lined and SS reactors for global pharmaceutical markets.
Reactor Capacity & Scale
Versatile reactor volumes ranging from 500L to 5,000L with operational capabilities from cryogenic (-78—C) to high-temperature reactions.
Key Reaction Capabilities
Hydrogenation, halogenation, peptide coupling, chiral reductions, crystallization, and cleanroom powder isolation.
Quality & Regulatory Compliance
Audited facilities operating in accordance with cGMP, ICH Q7 standards, with complete documentation including DMF and CTD dossiers.
Environmental & Safety Commitment
Zero liquid discharge (ZLD) effluent treatment plants, automated solvent recovery systems, and safety-first manufacturing culture.