Pharmaceutical Active Ingredient Division (Pharmaceutical Research Headquarters) Business and Technology
Process optimization is possible! We propose a balanced active pharmaceutical ingredient development plan that considers speed, cost-effectiveness, and quality.
We would like to introduce our pharmaceutical active ingredient division (Pharmaceutical Research Headquarters) and its business and technology. We flexibly utilize a network of reliable partner contract manufacturers to build and propose an optimal active ingredient manufacturing supply chain tailored to specific purposes. With world-class pharmaceutical development technology and assured quality, we provide "the development of active ingredient manufacturing methods from 'zero' that meet global application requirements" and "a seamless and consistent active ingredient manufacturing process and quality design from preclinical stages to obtaining marketing approval." 【Features】 ■ Development of active ingredient manufacturing methods from 'zero' based on technology and know-how cultivated over many years at major domestic pharmaceutical companies. ■ Establishment of active ingredient manufacturing methods and quality design according to development stages and applications. ■ Flexible response to active ingredient manufacturing requests. ■ Accurate support for application processes (clinical trials and commercial use). *For more details, please refer to the PDF materials or feel free to contact us.
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【Distinctive Technologies Held】 ■ World-class asymmetric catalyst technology ■ Manufacturing method settings according to development stages ■ Scale-up simulation technology ■ High-sensitivity analytical technology supporting impurity management ■ Establishment of robust manufacturing methods utilizing QbD experiments ■ Active pharmaceutical ingredient crystallization technology ■ Drug discovery support ■ Flow chemistry ■ Consultation on active pharmaceutical ingredient synthesis process development *For more details, please refer to the PDF document or feel free to contact us.
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【Consultation Examples】 ■ Consultation on the establishment of manufacturing methods for active pharmaceutical ingredients (APIs) and quality design according to development stage and application ■ Consultation regarding the API manufacturing supply chain ■ Consultation on the production of chiral compounds ■ Consultation related to API operations for Phase 1 trials *For more details, please refer to the PDF document or feel free to contact us.
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Company information
Our company is a pharmaceutical CMC research and development contract company that spun out from the CMC research division of Takeda Pharmaceutical Company Limited in July 2017. We support excellent pharmaceutical development as experts in CMC research. Our research team consists of experts with extensive experience and achievements in process chemistry, formulation research and development, and analytical testing development related to CMC research. We provide high-level services and solutions tailored to our customers' needs across each process from the early stages of pharmaceutical development to application, while flexibly collaborating. We have established a collaborative system with partner companies, enabling us to offer a one-stop service. Please utilize us as a platform for your pharmaceutical development.