Products with increased safety, compliant with the standards of the US Food and Drug Administration (FDA) and other countries’ regulatory authorities
We manufacture active pharmaceutical ingredients and drug intermediates under good manufacturing practices (GMP) and in compliance with the latest regulations on manufacturing and quality control. The world-class quality of our products not only meets the requirements of the Japanese Pharmaceutical Affairs Law but also passes audits by the US FDA as well as those by UK Medicines & Healthcare Products Regulatory Agency (MHRA). We ensure the high quality and safety of our products.
Contract manufacturing of new drugs and generics with high-level technology that allows us to meet customers’ needs
With the advent of a super-aging society, the demand for healthcare and medical products is steadily rising, resulting in increasingly fierce competition in the development of drugs. In response, we have strengthened our business in contract manufacturing of active pharmaceutical ingredients and drug intermediates for new drugs and generics. We are ready to meet diverse needs of customers with our own manufacturing process established by our enhanced Industrialization Department, our cutting-edge manufacturing facilities, and a quality assurance system that meets international standards.
Global marketing of products developed by our company to contribute to the health of a broader range of people
We manufacture and market protamine sulfate, an active ingredient developed by our company to be used for insulin preparations; isoniazid, an active ingredient of anti-tuberculosis therapeutic agents; and trifluorothymidine, an antiviral ophthalmic solution. With these products, we contribute to the health of many people. We will continue to meet the diverse needs of customers with our expertise and manufacturing technology gained through our experience in research and development as well as products manufactured at our sophisticated facilities.