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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PharmaCompass offers a list of Resmetirom API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Resmetirom manufacturer or Resmetirom supplier for your needs.
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PharmaCompass also assists you with knowing the Resmetirom API Price utilized in the formulation of products. Resmetirom API Price is not always fixed or binding as the Resmetirom Price is obtained through a variety of data sources. The Resmetirom Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
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.
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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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