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U.S. FDA Issues Warning Letter To Tomita For GMP Deficiencies

This article was originally published in PharmAsia News

Executive Summary

The U.S. FDA issued a Jan. 14 warning letter to Tokushima, Japan-based Tomita Pharmaceutical Co. for "significant deviations" from U.S. current good manufacturing practices in Tomita's manufacturing of active pharmaceutical ingredients

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PharmAsia News Business Bulletin

A regular roundup of commercial stories appearing in Scrip’s sister publication PharmAsia News, whose multilingual team of regional experts provides authoritative business intelligence focused on the Asian marketplace. Full stories can be accessed by clicking on the story title (subscription required).

PharmAsia News Business Bulletin

A regular roundup of commercial stories appearing in Scrip’s sister publication PharmAsia News, whose multilingual team of regional experts provides authoritative business intelligence focused on the Asian marketplace. Full stories can be accessed by clicking on the story title (subscription required.)

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