Active Pharmaceutical Ingredients (APIs)

Active Pharmaceutical Ingredients (APIs)

From route scouting to batch execution, the journey of bringing APIs to our manufacturing facility is carried out with great diligence by our highly knowledgeable team. Our R&D team is dedicated to developing processes that are cost-effective and consistent. Additionally, our manufacturing facility is designed to prioritize quality as the central focus of our API production. We implement stringent quality control measures at every production stage, employing advanced analytical techniques to ensure compliance with internal standards and regulatory requirements, safeguarding the safety of our people and efficacy of our products.

Competitive global prices with quality and consistent production.

Globally recognized, WHO GMP certified manufacturing plant.

ISO 9001:2015 Certified for R&D Lab.

Reliable customer support through knowledge transfer and documentation support.

Manufacturing facility Production Capacity:

Key Highlights:

  • Stain less Steel and Mild Steel Glass lined Reactors (0.1 KL to 10 KL) – Total Volume of Plant: 300 KL
  • Pressure reactors (2 KL to 3 KL) – Operating pressure up to 12 KG/CM2
  • Cryogenic reactors (0.5 KL – 8 KL)
  • Clean rooms (ISO Class – 8)
  • Reaction temperatures (−100 °C to +250 °C)

Dryers:

  • ANFDs (3 KL – 5 KL)
  • RCVDs (0.5 KL – 2 KL)
  • Tray dryers (TD) (48 Trays – 96 Trays)
  • Vacuum tray dryers (VTD) (24 Trays –  96 Trays)
  • Fluidised bed dryer (FBD) (250 KG)

Physical Operations:

  • Micronizers
  • Sifters
  • Milling
  • Blenders

DM water system

ZLD unit with 190 KL capacity