Our manufacturing facilities are strategically located in Vasai, Palghar District, Maharashtra, India, approximately 60 km from CSIA(Mumbai) and 55 km from (JNPT), India's largest container seaport. Spread across 48,000 Sq Ft It features dedicated production lines that are designed with WHO-GMP & PIC/S standards, ensuring the production of high-quality pharmaceutical products under controlled and validated conditions.
60,000–80,000 tubes per day
12,000–15,000 units per day
Up to 2–4 million tablets per day
40,000 tubes per day
Each production area is well equipped with area-classified cleanrooms, dedicated HVAC systems, automated process control systems, and validated utilities, supported by scientifically designed contamination control strategies to ensure product integrity, operational excellence.
The Oral Solid Dosage (OSD) facility is designed yo manufacture tablets with dedicated manufacturing and packaging lines for potent and non-potent products, ensuring segregation, effective contamination control, and compliance with current Good Manufacturing Practices (cGMP). The production lines house segregated granulation, blending, compression, coating, and packaging lines.
The Non-Sterile Semi-Solid facility is equipped with dedicated manufacturing, filling, and packing lines for potent and non-potent products, ensuring segregation, contamination control and compliance with cGMP requirements. The facility specializes in the manufacture of creams, ointments, gels, and other topical formulations.
The Small Volume Parenteral (SVP) facility manufactures and fills sterile injectables in ampoules and vials. Key operations include aseptic manufacturing and processing, all performed in controlled cleanrooms using validated aseptic processes to ensure quality and patient safety.
The Sterile Semi-solid facility is designed with classified cleanrooms, environmental monitoring, and stringent contamination control measures for the manufacturing and filling of sterile topical pharmaceutical products. The facility is can manufacture sterile preparations both with Aseptic processing and terminal sterilization.
Our GLP approved QC and microbiology is equipped with all advanced analytical instruments to ensure comprehensive testing of all raw and packaging materials, in-process and finished product, and stability samples. We carry out our own in house validation and qualification studies and we routinely carry out stability studies in zone IV B
We have a dedicated QA section that has separate facilities and personnel specialized in various areas associated to a robust Quality Management System (QMS). We have adopted the principles of WHO, PIC/S and guidelines as issued by many country MOHs into our QMS in order to reflect the current expectations of regulators across various geographies.
An integrated ERP/LIMS and DMS which has access control and audit trails for each step right from product development to the end stage of dispatch
Dedicated in process QA monitoring and testing for each production section.
Effective document storage, retrieval and backup system (both electronic and paper based) to ensure compliance and documentation trails during the entire product life cycle.
Dedicated training infrastructure and personal Learning and development (LnD) system to incorporate training as a daily part of work duties across the organization.
We have a separate Regulatory affairs team that manages product registrations, technical documentation, regulatory submissions, lifecycle management, and global compliance activities, ensuring adherence to the regulatory requirements of domestic and international markets.
Our facility boasts a highly qualified and committed engineering section and an in-house automation and IT team which help with tight integration of our manufacturing processes with machines and IT infrastructure. Our aim is a sustained yet gradual push towards industry 4.0, intelligent automation and ever-increasing efficiency. They also ensure timely and robust upkeep of our utilities support facilities like HVAC, water and compressed air systems ensuring quality efficiency and compliance.
