01 1M/sUnimark Remedies Limited
01 1Ganciclovir USP
01 1WC-0170
01 1India
Date of Issue : 2024-04-23
Valid Till : 2027-04-22
Written Confirmation Number : WC-0170
Address of the Firm : Plot No. 41, 42/2, 42/1/B, 43, 40, 59, 58 GIDC, Vapi, Dist: Valsad -396195, Guja...
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PharmaCompass offers a list of Ganciclovir 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 Ganciclovir manufacturer or Ganciclovir supplier for your needs.
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PharmaCompass also assists you with knowing the Ganciclovir API Price utilized in the formulation of products. Ganciclovir API Price is not always fixed or binding as the Ganciclovir Price is obtained through a variety of data sources. The Ganciclovir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 2'-NDG manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 2'-NDG, including repackagers and relabelers. The FDA regulates 2'-NDG manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 2'-NDG 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 2'-NDG manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 2'-NDG supplier is an individual or a company that provides 2'-NDG active pharmaceutical ingredient (API) or 2'-NDG finished formulations upon request. The 2'-NDG suppliers may include 2'-NDG API manufacturers, exporters, distributors and traders.
click here to find a list of 2'-NDG suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 2'-NDG written confirmation (2'-NDG WC) is an official document issued by a regulatory agency to a 2'-NDG manufacturer, verifying that the manufacturing facility of a 2'-NDG active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting 2'-NDG APIs or 2'-NDG finished pharmaceutical products to another nation, regulatory agencies frequently require a 2'-NDG WC (written confirmation) as part of the regulatory process.
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