API Chemical Synthesis Reactors
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Manufacturing · Division 03

Active Pharmaceutical Ingredients, engineered with process discipline.

Our API division synthesises bulk active ingredients under stringent process controls, backed by full analytical DMF documentation to support regulatory filings in India and international markets.

Regulatory Ready Dossiers

DMF Filing Support

Full analytical validation, impurity profiling, and ICH stability packages prepared to support your market filings.

SS 316L
Glass-Lined Reactors
ICH
Stability Guidelines
Core Capabilities

Process capabilities built for regulated bulk supply.

Multi-purpose reactors

Glass-lined & SS 316L reactors sized from pilot batches to commercial volumes.

Analytical R&D

Method development, validation protocols & genotoxic impurity profiling.

Process validation

Scale-up protocols with documented batch-to-batch process consistency.

DMF documentation

Drug Master File preparation and active regulatory support for customer filings.

Effluent & solvent recovery

Environmentally compliant closed-loop solvent recovery & ETP systems.

Bulk packaging

HDPE drums, fibre drums & validated temperature-controlled logistics.

Regulatory Support

Documentation built to support your filing timeline.

Our regulatory affairs team works alongside customers from early feasibility through commercial supply — providing analytical data and stability packages expected by authorities.

  • Certificate of Analysis (CoA) provided with every batch shipment

  • Real-time & accelerated stability packages aligned to ICH guidelines

  • Comprehensive impurity profiling & genotoxic impurity assessment

  • Site Master File (SMF) access and support for partner quality audits

Analytical QC Laboratory
ICH Stability Compliant
Analytical & Impurity Testing Lab
Facility Snapshot

Plant capabilities at a glance.

Reactor capacityMulti-purpose SS 316L & glass-lined reactors from pilot to commercial-scale volumes
DocumentationDMF Dossiers, CoA, ICH stability data & site master files upon request
CertificationsWHO-GMP · ISO 9001:2015 · ISO 14001:2015 · Environmental Board Clearance
Quality controlDedicated analytical R&D laboratory with HPLC, GC, and impurity testing capabilities
Supply termsEx-works and CIF terms available for domestic and international export shipments

Need an API sourcing or DMF partner?

Share your molecule and target specification — our regulatory team will follow up with documentation and technical feasibility.

Request DMF / Specs