A 100% export-oriented pharmaceutical organization with three advanced manufacturing units, built to meet national and international regulatory standards. Our facilities are designed with modern automation, controlled material flow, and scalable production capabilities.
Trusted Infrastructure for Global Supply
Quality at the Core ofInfrastructure
Manufacturing Facilities
Focus on scale, automation, dosage forms, and export readiness.
Three export-oriented manufacturing units equipped for oral solids, infusions, topical formulations, ophthalmic products, and SVP manufacturing. Designed with automated systems, controlled workflows, and scalable production capacity.
Regulatory Compliance
Focus on certifications, inspections, and global approvals.
Manufacturing units are approved by WHO GMP and inspected by multiple international regulatory authorities, ensuring consistent compliance with evolving global pharmaceutical standards.
Quality Control & Microbiology
Focus on testing capability, instruments, and accuracy.
Well-established in-house laboratories supported by modern analytical instruments ensure timely, accurate testing of raw materials, packaging materials, and finished products as per approved specifications.
Quality Assurance & Regulatory Affairs
Focus on lifecycle monitoring and dossier expertise.
Dedicated QA and RA teams oversee quality across the product lifecycle, including validation, stability studies, audits, and dossier preparation in CTD, eCTD, and ACTD formats.
Engineering & Utilities
Focus on utilities and compliance-driven infrastructure.
Experienced engineering teams manage purified water systems, HVAC, steam, and compressed air utilities to meet stringent regulatory norms and manufacturing requirements.
Warehousing & Logistics
Focus on storage control and distribution readiness.
Company-owned warehouses ensure safe storage of raw materials and finished products under controlled temperature and humidity conditions until final distribution.
Digital & Data Management
Focus on IT systems, traceability, and data integrity.
Robust IT infrastructure supports data generation, monitoring, and processing across manufacturing, quality, and warehousing functions, ensuring data integrity and traceability.
A structured approach to quality-driven pharmaceutical production
Manufacturing ProcessWorkflow
This manufacturing flowchart outlines the step-by-step process followed across our facilities, ensuring consistency, safety, and regulatory compliance at every stage. From raw material handling to final quality release and dispatch, each operation is carefully monitored and executed in alignment with global pharmaceutical manufacturing standards.
All raw materials are stored in controlled environments and dispensed through validated systems. Sampling and bulk analysis are performed to ensure compliance with approved specifications before processing.
Component Preparation & Sterilization
Ensuring sterility of critical components
Vials and rubber bungs undergo automated washing, sterilization, and depyrogenation processes. These operations are conducted in dedicated areas to maintain aseptic integrity
Formulation, Mixing & Filtration
Precision formulation under controlled conditions
Single or multiple ingredient formulations are prepared in validated mixing vessels. Solutions are filtered through 0.22 µ filters, supported by nitrogen purging to maintain product stability and sterility.
Aseptic Filling & Sealing Operations
Maintaining sterility during critical operations
Aseptic filling and bunging are carried out in controlled environments, followed by vial sealing. Continuous in-process quality assurance (IPQA) ensures adherence to predefined quality parameters.
Visual Inspection & Quality Checks
Every unit examined for safety and consistency
Each filled vial undergoes visual inspection to detect defects or particulates. Sampling and testing are performed in accordance with regulatory standards.
Labeling, Coding & Traceability
Complete product identification and compliance
Accurate labeling and coding ensure full traceability of batches. All labeling activities are verified to meet regulatory and client-specific requirements.
Secondary & Tertiary Packaging
Export-ready packaging solutions
Products are packed using cartons, shippers, leaflets, and trays under controlled conditions. Packaging integrity and labeling accuracy are verified before shipment.
Quality Release & Global Dispatch
Approved by QA, delivered worldwide
Finished goods are quarantined until final QA approval. Upon release, products are dispatched through secure logistics channels to global markets, ensuring timely and compliant delivery.
