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01 1D. K. PHARMA CHEM PRIVATE LIMITED Badlapur IN
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01 1Tosylchloramide sodium
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01 1India
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01 1Valid
Certificate Number : CEP 2022-217 - Rev 00
Status : Valid
Issue Date : 2024-06-03
Type : Chemical
Substance Number : 381
100
PharmaCompass offers a list of Chloramine-T 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 Chloramine-T manufacturer or Chloramine-T supplier for your needs.
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PharmaCompass also assists you with knowing the Chloramine-T API Price utilized in the formulation of products. Chloramine-T API Price is not always fixed or binding as the Chloramine-T Price is obtained through a variety of data sources. The Chloramine-T Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Gansil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gansil, including repackagers and relabelers. The FDA regulates Gansil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gansil 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 Gansil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Gansil supplier is an individual or a company that provides Gansil active pharmaceutical ingredient (API) or Gansil finished formulations upon request. The Gansil suppliers may include Gansil API manufacturers, exporters, distributors and traders.
click here to find a list of Gansil suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Gansil CEP of the European Pharmacopoeia monograph is often referred to as a Gansil Certificate of Suitability (COS). The purpose of a Gansil CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Gansil EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Gansil to their clients by showing that a Gansil CEP has been issued for it. The manufacturer submits a Gansil CEP (COS) as part of the market authorization procedure, and it takes on the role of a Gansil CEP holder for the record. Additionally, the data presented in the Gansil CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Gansil DMF.
A Gansil CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Gansil CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Gansil suppliers with CEP (COS) on PharmaCompass.