Manufacturing Facility

Compliant. Scalable. Built for Quality.

Schedule M (Revised), WHO‑GMP and GLP aligned infrastructure with end‑to‑end control.

Plant Area & Infrastructure

Located in A‑1 Ratan Industrial Area, Harsuliya, Jaipur, our unit spans over 33,000 sq. ft. with an additional 20,000 sq. ft. earmarked for expansion.

  • Dedicated zones for oral tablets, oral liquids, and external solutions
  • ISO‑classified cleanroom areas with controlled airflow systems
  • In‑house QC lab for physical, chemical, and microbial testing
  • Temperature & humidity‑controlled storage areas
  • 10,000+ sq. ft. of world-class warehouse space with optimized inventory management
Schedule M (Revised) WHO‑GMP GLP
Cleanroom and production areas

Manufacturing Capacities

Large‑scale output with flexibility for custom batch sizes.

Product Type Daily Capacity
Oral Tablets Up to 25 Lakhs units
Oral Liquids 40,000 bottles
External Solutions Custom production volumes based on requirements

Comprehensive Processes, End‑to‑End Control

Tablet manufacturing processes

Oral Tablets

  • Granulation (wet/dry)
  • High‑speed rotary compression
  • Film and sugar coating
  • Metal detection & de‑dusting
  • Blister, strip, and alu‑alu packaging
Liquid manufacturing processes

Oral Liquids

  • Stainless steel mixing tanks
  • Homogenization & filtration
  • Automatic bottle filling & capping
  • Labeling and shrink wrapping
External solutions manufacturing

External Solutions

  • Jacketed mixing vessels
  • Filling & sealing lines
  • Validated cleaning & formulation protocols

Flexible Packaging Solutions to Match Every Need

Primary Packaging

  • Tablets: Strip, Blister, Alu‑Alu
  • Liquids: Bottles (Pilfer‑proof or CRC caps)

Client Flexibility

  • Clients may provide raw materials and packaging components
  • White‑label production and customized branding

Quality Assurance & Analytical Capabilities

Our advanced in-house Quality Control laboratory is equipped with state-of-the-art analytical instruments to ensure every product meets the highest standards of quality, safety, and compliance.

Key Capabilities

  • In-house Gas Chromatography (GC) for Ethylene Glycol (EG) and Diethylene Glycol (DEG) analysis
  • Chemical and microbiological testing
  • Faster turnaround times with rapid in-house analysis
  • Enhanced quality assurance through accurate and reliable testing
  • Greater process control for consistent product quality
  • Batch traceability and comprehensive documentation
  • Standard Operating Procedures (SOPs) aligned with regulatory requirements
  • Stability testing and real-time quality monitoring
  • Internal quality audits to ensure continuous compliance and improvement
Quality control laboratory
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