China’s top API & intermediate manufacturer, delivering advanced CMO/CDMO solutions to 60+ countries, empowering global health progress
01 1Shandong Chenghui Shuangda Pharmaceutical Co., Ltd.
01 1Meldonium Dihydrate
01 1SD240035
01 1China
China’s top API & intermediate manufacturer, delivering advanced CMO/CDMO solutions to 60+ countries, empowering global health progress
Date of Issue : 2024-07-10
Valid Till : 2027-07-09
Written Confirmation Number : SD240035
Address of the Firm : Economic Development Zone, Pingyuan County, Dezhou City, Shandong
88
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A Mildronate dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mildronate dihydrate, including repackagers and relabelers. The FDA regulates Mildronate dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mildronate dihydrate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Mildronate dihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Mildronate dihydrate supplier is an individual or a company that provides Mildronate dihydrate active pharmaceutical ingredient (API) or Mildronate dihydrate finished formulations upon request. The Mildronate dihydrate suppliers may include Mildronate dihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Mildronate dihydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Mildronate dihydrate written confirmation (Mildronate dihydrate WC) is an official document issued by a regulatory agency to a Mildronate dihydrate manufacturer, verifying that the manufacturing facility of a Mildronate dihydrate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Mildronate dihydrate APIs or Mildronate dihydrate finished pharmaceutical products to another nation, regulatory agencies frequently require a Mildronate dihydrate WC (written confirmation) as part of the regulatory process.
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