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API Manufacturing Process

Api Manufacturing Process

We provide manufacture and supply of Active Pharmaceutical Ingredients (APIs) on an integrated manufacturing model across North America, Europe and Asia. Our manufacturing facilities with API finishing facilities meet global regulatory requirements, cGMP compliance standards and are FDA inspected and approved.

We hold a successful performance record of over 40 years of supplying API to US and European markets from our facilities located in Canada, India and the UK. With a reactor volume exceeding 500 KL including pilot plants and multi-purpose plants, we are capable of executing extensive API requirements of our clients.

Services Offered

Manufacturing and Supply of

  • Key Starting Materials (KSMs)
  • Registered Starting Materials (RSMs)
  • Key GMP Intermediates
  • Commercial scale APIs

Commercial Capabilities

  • Flexible Containment facility
  • cGMP multi-purpose pilot plants
  • Total reactor capacity of › 500 KL
  • Handling of toxic gases & moisture sensitive compounds
  • Enzymatic reactions


  • Torcan, Canada
  • Digwal, India
  • Ennore, India
  • Morpeth, UK