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Process Research and Development
 
Taj recognizes that the ultimate goal of API synthesis is to scale-up from milligram quantities at the lab bench to kilogram quantities in a pilot plant. We also understand that at the clinical supply stage, process development becomes increasingly complex. With over 220 combined years of experience at our Oxford, UK, site, 180 years at our Missouri, US, site, and over 170 years' process chemistry experience in our senior staff in India, Taj's chemists are recognized as experts in process optimization for API scale up, as well as for novel route development. Taj's Oxford and Missouri facilities have been FDA inspected, and, additionally, the MHRA has inspected and approved the UK site.

At Taj, we can help you deal quickly and safely with the challenges and complexities of scale-up. Our staff and facilities work toward an API synthesis process that is:

  • Robust
  • Quick
  • Transferable
  • Cost-effective
  • Safe

Our goal is to help you lock in your process parameters so that they may be transferred to any other facility as the product evolves in development. We can also produce batches of API, scaled to the specific demands of clinical trials.



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