Shandong Loncom is an R&D-focused manufacturer of Anti-cancer APIs.

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01 1Shandong Loncom Pharmaceutical Co Ltd.
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01 1Resmetirom
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01 1SD250051
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01 1China
Date of Issue : 2025-04-07
Valid Till : 2028-05-08
Written Confirmation Number : SD250051
Address of the Firm : No. 127, Qizhong Avenue, Qihe County, Dezhou City, Shandong Province, China
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A Resmetirom (MGL-3196) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Resmetirom (MGL-3196), including repackagers and relabelers. The FDA regulates Resmetirom (MGL-3196) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Resmetirom (MGL-3196) 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 Resmetirom (MGL-3196) supplier is an individual or a company that provides Resmetirom (MGL-3196) active pharmaceutical ingredient (API) or Resmetirom (MGL-3196) finished formulations upon request. The Resmetirom (MGL-3196) suppliers may include Resmetirom (MGL-3196) API manufacturers, exporters, distributors and traders.
click here to find a list of Resmetirom (MGL-3196) suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Resmetirom (MGL-3196) written confirmation (Resmetirom (MGL-3196) WC) is an official document issued by a regulatory agency to a Resmetirom (MGL-3196) manufacturer, verifying that the manufacturing facility of a Resmetirom (MGL-3196) active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Resmetirom (MGL-3196) APIs or Resmetirom (MGL-3196) finished pharmaceutical products to another nation, regulatory agencies frequently require a Resmetirom (MGL-3196) WC (written confirmation) as part of the regulatory process.
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