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01 1M/s. Apitoria Pharma Private Limited
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01 1Nirmatrelvir IH
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01 1WC-0023
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01 1India
Date of Issue : 2022-06-07
Valid Till : 2025-06-25
Written Confirmation Number : WC-0023
Address of the Firm : Survey no. 52,53,58,59,61 to 78,127&128, Pydibhimanvaram Village &Sy.No. 1,2,4t0...
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PharmaCompass offers a list of Nirmatrelvir 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 Nirmatrelvir manufacturer or Nirmatrelvir supplier for your needs.
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PharmaCompass also assists you with knowing the Nirmatrelvir API Price utilized in the formulation of products. Nirmatrelvir API Price is not always fixed or binding as the Nirmatrelvir Price is obtained through a variety of data sources. The Nirmatrelvir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Paxlovid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Paxlovid, including repackagers and relabelers. The FDA regulates Paxlovid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Paxlovid 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 Paxlovid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Paxlovid supplier is an individual or a company that provides Paxlovid active pharmaceutical ingredient (API) or Paxlovid finished formulations upon request. The Paxlovid suppliers may include Paxlovid API manufacturers, exporters, distributors and traders.
click here to find a list of Paxlovid suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Paxlovid written confirmation (Paxlovid WC) is an official document issued by a regulatory agency to a Paxlovid manufacturer, verifying that the manufacturing facility of a Paxlovid active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Paxlovid APIs or Paxlovid finished pharmaceutical products to another nation, regulatory agencies frequently require a Paxlovid WC (written confirmation) as part of the regulatory process.
click here to find a list of Paxlovid suppliers with Written Confirmation (WC) on PharmaCompass.
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