[ Manufacturing Capabilities ]

World-Class Delivery

Our robust manufacturing processes, along with our commitment to quality, compliance, and employee training, ensure that we deliver safe, effective, and high-quality pharmaceutical products to our customers.

  • Manufacturing activities under controlled environmental conditions (ISO class-8 with temperature & RH control)
  • Prior to the start of manufacturing and packing, line clearance is performed to prevent cross-contamination and ensure a sterile environment.
  • We use only qualified equipment, which is maintained under a rigorous program to ensure continuous operational control.
  • All manufacturing and packing are carried out according to approved batch records, ensuring strict adherence to regulatory standards and consistency in every batch.
  • Our trained personnel operate equipment in full compliance with current Good Manufacturing Practice (cGMP) guidelines, safeguarding product quality and safety.
  • We perform thorough process validations, including cleaning validations and hold-time studies, to guarantee product performance and compliance.
  • Periodic and On-the-Job training is conducted to ensure our teams are continuously updated on cGMP requirements and best practices.

[ Lab Capabilities ]

Smart Science, Safer Drugs

We are pioneers in pharmaceutical quality control with cutting-edge laboratory technologies, ensuring precision, compliance, and reliability in every batch.

  • Comprehensive Analytical Expertise – In-depth QC analysis of raw materials, in-process samples, and finished products using validated methodologies for consistency and efficacy.
  • Advanced Instrumentation – Equipped with HPLC, GC, FTIR Spectroscopy, Atomic Absorption Spectrophotometry, and Malvern Particle Size Analysis.
  • Regulatory Excellence & Data Integrity – Operating under strict compliance with USFDA, WHO-GMP, and global regulatory standards.
  • Stability & Environmental Monitoring – Controlled stability chambers ensure product efficacy and safety throughout shelf life.
  • Quality Control & Scientific Rigor – Implementing GLP, equipment qualification, calibration, and robust data management.

Our commitment to quality and innovation ensures pharmaceuticals that exceed industry expectations

[ Automation ]

Driving Efficiency & Compliance​

We are investing heavily in robotics and futuristic technology to strengthen automation, aiming for a future driven by intelligent technology. This focus enables us to minimize human error, optimize processes, and maintain the highest standards of global regulatory compliance.. Our facility is equipped with automated systems and monitoring technologies that enhance manufacturing consistency.​

  • Automated Equipment Cleaning & Maintenance– Ensuring high-level hygiene & compliance​
  • Process Monitoring & Control Systems – Maintaining optimal manufacturing conditions​
  • Automated Line Clearance & Batch Processing– Reducing manual interventions for improved efficiency​ efficiency
  • Real-Time Data Capture & Analysis – Enabling better decision-making and process optimization​

By integrating automation into our manufacturing and quality operations, we are able to reduce human error, enhance process control, and ensure regulatory compliance with global standards.​

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