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Kaneka manufactures many products to meet GMP regulations. Kaneka's QA&QC system and facilities have been routinely audited and approved by leading pharmaceutical companies. They have also been inspected and approved by government authorities including the US-FDA. Our QA&QC system supports the manufacture of API's and intermediates.
Kaneka has submitted U.S. and European Drug Master Files for selected products. New submissions will be made, as required. |
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| Kaneka is committed to the implementation of the Responsible Care Programs established by the Japan Responsible Care Council consisting of several activities with regard to process safety, disaster prevention, environmental preservation, occupational health and safety, chemical and product safety and logistics safety. Assessment of the impact of our activities on both the public and the environment is published in our Responsible Care Reports. |
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