We are delighted to inform you that, we have acquired a fully equipped state-of-the-art manufacturing facility wherein we can undertake manufacturing of RSMs, intermediates, APIs and NCEs. The facility has a cGMP pilot plant, intermediate area and also ISO class 8 clean rooms.
We can now support your drug substance to move more rapidly through the value chain. We will be able to assist you in accelerated process development and scale-up under GMP and non-GMP compliance. In addition to supporting early phase programs, including IND-enabling projects, our team will now be able to assist you in drug substance supply for clinical trials and commercial manufacturing. We endeavor to be your comprehensive service provider from bench scale to commercial scale manufacturing.
We are very excited about our enhanced capabilities and will continue to add greater value and more comprehensive suite of services.
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