01 1ZHEJIANG CHEMSYN PHARM. CO., LTD. Quzhou CN
01 1Sulfanilamide
01 1China
01 1Valid
Certificate Number : R1-CEP 2007-241 - Rev 01
Status : Valid
Issue Date : 2022-09-08
Type : Chemical
Substance Number : 1571
99
PharmaCompass offers a list of Sulfanilamide 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 Sulfanilamide manufacturer or Sulfanilamide supplier for your needs.
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PharmaCompass also assists you with knowing the Sulfanilamide API Price utilized in the formulation of products. Sulfanilamide API Price is not always fixed or binding as the Sulfanilamide Price is obtained through a variety of data sources. The Sulfanilamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A p-Aminobenzensulfonamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of p-Aminobenzensulfonamide, including repackagers and relabelers. The FDA regulates p-Aminobenzensulfonamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. p-Aminobenzensulfonamide 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 p-Aminobenzensulfonamide supplier is an individual or a company that provides p-Aminobenzensulfonamide active pharmaceutical ingredient (API) or p-Aminobenzensulfonamide finished formulations upon request. The p-Aminobenzensulfonamide suppliers may include p-Aminobenzensulfonamide API manufacturers, exporters, distributors and traders.
click here to find a list of p-Aminobenzensulfonamide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A p-Aminobenzensulfonamide CEP of the European Pharmacopoeia monograph is often referred to as a p-Aminobenzensulfonamide Certificate of Suitability (COS). The purpose of a p-Aminobenzensulfonamide CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of p-Aminobenzensulfonamide EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of p-Aminobenzensulfonamide to their clients by showing that a p-Aminobenzensulfonamide CEP has been issued for it. The manufacturer submits a p-Aminobenzensulfonamide CEP (COS) as part of the market authorization procedure, and it takes on the role of a p-Aminobenzensulfonamide CEP holder for the record. Additionally, the data presented in the p-Aminobenzensulfonamide CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the p-Aminobenzensulfonamide DMF.
A p-Aminobenzensulfonamide CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. p-Aminobenzensulfonamide CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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