01 1M/s. SNA Healthcare Pvt. Ltd.,
01 1Allantoin USP
01 1WC-0532
01 1India
Date of Issue : 2025-11-11
Valid Till : 2028-08-22
Written Confirmation Number : WC-0532
Address of the Firm : N-213/3, M.I.D.C. Tarapur, MIDC Tarapur Boisar, District: Thane-Zone4, Maharasht...
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PharmaCompass offers a list of Glyoxyldiureide 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 Glyoxyldiureide manufacturer or Glyoxyldiureide supplier for your needs.
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A Allantoin, European Pharmacopoeia (EP) Reference Standard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Allantoin, European Pharmacopoeia (EP) Reference Standard, including repackagers and relabelers. The FDA regulates Allantoin, European Pharmacopoeia (EP) Reference Standard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Allantoin, European Pharmacopoeia (EP) Reference Standard 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 Allantoin, European Pharmacopoeia (EP) Reference Standard supplier is an individual or a company that provides Allantoin, European Pharmacopoeia (EP) Reference Standard active pharmaceutical ingredient (API) or Allantoin, European Pharmacopoeia (EP) Reference Standard finished formulations upon request. The Allantoin, European Pharmacopoeia (EP) Reference Standard suppliers may include Allantoin, European Pharmacopoeia (EP) Reference Standard API manufacturers, exporters, distributors and traders.
click here to find a list of Allantoin, European Pharmacopoeia (EP) Reference Standard suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Allantoin, European Pharmacopoeia (EP) Reference Standard written confirmation (Allantoin, European Pharmacopoeia (EP) Reference Standard WC) is an official document issued by a regulatory agency to a Allantoin, European Pharmacopoeia (EP) Reference Standard manufacturer, verifying that the manufacturing facility of a Allantoin, European Pharmacopoeia (EP) Reference Standard active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Allantoin, European Pharmacopoeia (EP) Reference Standard APIs or Allantoin, European Pharmacopoeia (EP) Reference Standard finished pharmaceutical products to another nation, regulatory agencies frequently require a Allantoin, European Pharmacopoeia (EP) Reference Standard WC (written confirmation) as part of the regulatory process.
click here to find a list of Allantoin, European Pharmacopoeia (EP) Reference Standard suppliers with Written Confirmation (WC) on PharmaCompass.
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