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MANUFACTURING

MANUFACTURING

Augmenting Our Growth

Our cGMP standard production capability brings together scientific expertise and State-of-the-art technologies to support the chemical development and manufacturing of Active Pharmaceutical Ingredients, and Intermediates for a range of therapeutic categories.

As the preferred partner to international and domestic drug manufacturers, we empower ourselves with manufacturing capabilities to meet the strictest of demands and standards applicable worldwide. Flexible and with ready access to every resource required, we are capable of delivering our manufacturing at a competitive price point. We possess today the expertise to work on reactions that are also hazardous, including Cyanation, Chlorination, high pressure reactions and Diazotization.

Key Reactions

AT SAPTAGIR, WE COMPLY WITH ALL cGMP GUIDELINES, INCLUDING ENVIRONMENT, HEALTH & SAFETY (EHS) STANDARDS

  • GL and SS Reactors equipped with Heat Exchangers
  • High Vacuum Distillation
  • High Temperature and Cryogenic Reactions
  • Three - Class 1,00,000 complying clean rooms
  • Pilot block with attached clean room
  • GL and SS Reactors equipped with Heat Exchangers
  • High Vacuum Distillation
  • High Temperature and Cryogenic Reactions
  • Three - Class 1,00,000 complying clean rooms
  • Pilot block with attached clean room

Highlights Of Our Infrastructure

  • 32 Reactors
  • Volume 63 kL
  • Op. Range 50L-6.3 kL
  • Pilot Plant
  • Potential expansion to Block II & Block III
  • Clean Room I
  • Clean Room II
  • Clean Room III (Pilot Plant)
  • GL and SS Reactors equipped with Heat Exchangers
  • High Vacuum Distillation 
  • High Temperature and Cryogenic Reactions

Enquire Now

Product Enquiry

CAS Number : 65473-13-4