The outsourcing of production or the change of manufacturers entails complex processes. Our customers benefit from the experience of our team of experts with over 1,500 successfully completed transfer projects.
Each of our sites is specialized in a specific dosage form and/or API group. GMP is the standard at all of the sites; the majority of our facilities meet the requirements of the U.S. Food and Drug Administration (FDA) and the Japanese regulatory authority.
At our site in Japan, we also offer the special service of visually inspecting bulk drugs from Europe and the United States and to label and package them for the Japanese market. We can also offer this service for products that require cold chain storage.
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