World-Class
Infrastructure
Our manufacturing facility is purpose-built for precision pharmaceutical synthesis — equipped, validated, and continuously upgraded to meet the demands of a global industry.
Engineered for Precision Manufacturing
From raw material intake to final product dispatch, our facility is designed to maintain the integrity, purity, and consistency that pharmaceutical manufacturing demands.
Synthesis & Reaction Suites
Dedicated synthesis blocks equipped for multi-step organic chemistry, handling a wide range of reaction types including condensation, reduction, chlorination, and cyclization reactions.
Analytical Laboratory
In-house QC lab equipped for HPLC, GC, IR spectroscopy, and wet chemistry analysis — enabling rapid in-process testing and final product release with full traceability.
Temperature-Controlled Storage
Pharmaceutical-grade raw material and finished product storage with controlled temperature and humidity zones, ensuring material integrity from receipt to dispatch.
Purification Systems
Advanced purification infrastructure including solvent recovery, crystallization suites, and drying systems — delivering consistently high-purity intermediates batch after batch.
EHS-Compliant Infrastructure
Facility designed and operated in full compliance with environmental, health, and safety regulations — including effluent treatment, solvent handling, and worker safety systems.
Packaging & Dispatch
Pharmaceutical-grade packaging operations ensuring product protection, tamper-evidence, and regulatory labeling compliance for domestic and export-grade shipments.
A Facility That Grows With Industry Demands
Since inception, Sri Gayathri Drugs has continuously invested in facility enhancements, equipment upgrades, and process improvements. Our infrastructure today reflects over 22 years of refinement.
Founder ASRK Reddy's hands-on experience in setting up new manufacturing facilities — gained at Dr. Reddy's Laboratories — informs every infrastructure decision we make, ensuring our capabilities stay ahead of customer requirements.
Discuss Your Requirements →Scale-Up Capability
Proven ability to scale laboratory processes to commercial production volumes with process integrity maintained throughout.
GMP-Oriented Operations
Manufacturing operations aligned with Good Manufacturing Practice principles for pharmaceutical intermediates and APIs.
Trained Workforce
A skilled team of chemists, operators, and QC analysts continuously trained in operational safety, quality, and process improvement.