Comhony Biotech manufactures fermentation & semi-synthetic APIs which aim at dermatology, anti-biotics; mitochondria & memory health.
01 1Fujian Comhony Biotechnology Co., Ltd
01 1Sodium Fusidate
01 1FJ260012
01 1China
Comhony Biotech manufactures fermentation & semi-synthetic APIs which aim at dermatology, anti-biotics; mitochondria & memory health.
Date of Issue : 2024-03-13
Valid Till : 2029-03-04
Written Confirmation Number : FJ260012
Address of the Firm : No. 2, Nangang Road, Jiangyin Gangcheng Economic, Zone, Fuqing, Fuzhou City, Fuj...
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A Sodium Fusidate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Fusidate, including repackagers and relabelers. The FDA regulates Sodium Fusidate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Fusidate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Sodium Fusidate supplier is an individual or a company that provides Sodium Fusidate active pharmaceutical ingredient (API) or Sodium Fusidate finished formulations upon request. The Sodium Fusidate suppliers may include Sodium Fusidate API manufacturers, exporters, distributors and traders.
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A Sodium Fusidate written confirmation (Sodium Fusidate WC) is an official document issued by a regulatory agency to a Sodium Fusidate manufacturer, verifying that the manufacturing facility of a Sodium Fusidate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Sodium Fusidate APIs or Sodium Fusidate finished pharmaceutical products to another nation, regulatory agencies frequently require a Sodium Fusidate WC (written confirmation) as part of the regulatory process.
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