Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
01 1EVONIK OPERATIONS GMBH Hanau DE
02 1ARKEMA FRANCE Colombes FR
03 1SOLVAY CHEMIE B.V. HERTEN NL
01 1Hydrogen peroxide solution (3 per cent)
02 2Hydrogen peroxide solution (30 per cent)
01 1France
02 1Germany
03 1South Korea
01 3Valid
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
Hydrogen Peroxide Solution (30 Per Cent)
Certificate Number : CEP 2018-079 - Rev 04
Status : Valid
Issue Date : 2024-03-28
Type : Chemical
Substance Number : 396
Hydrogen Peroxide Solution (3 Per Cent)
Certificate Number : CEP 2022-162 - Rev 01
Status : Valid
Issue Date : 2024-02-27
Type : Chemical
Substance Number : 395
Hydrogen Peroxide Solution (30 Per Cent)
Certificate Number : R0-CEP 2018-167 - Rev 00
Status : Valid
Issue Date : 2020-07-22
Type : Chemical
Substance Number : 396
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PharmaCompass offers a list of Hydrogen Peroxide 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 Hydrogen Peroxide manufacturer or Hydrogen Peroxide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydrogen Peroxide manufacturer or Hydrogen Peroxide supplier.
PharmaCompass also assists you with knowing the Hydrogen Peroxide API Price utilized in the formulation of products. Hydrogen Peroxide API Price is not always fixed or binding as the Hydrogen Peroxide Price is obtained through a variety of data sources. The Hydrogen Peroxide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Oxydol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxydol, including repackagers and relabelers. The FDA regulates Oxydol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxydol 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 Oxydol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxydol supplier is an individual or a company that provides Oxydol active pharmaceutical ingredient (API) or Oxydol finished formulations upon request. The Oxydol suppliers may include Oxydol API manufacturers, exporters, distributors and traders.
click here to find a list of Oxydol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Oxydol CEP of the European Pharmacopoeia monograph is often referred to as a Oxydol Certificate of Suitability (COS). The purpose of a Oxydol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Oxydol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Oxydol to their clients by showing that a Oxydol CEP has been issued for it. The manufacturer submits a Oxydol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Oxydol CEP holder for the record. Additionally, the data presented in the Oxydol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Oxydol DMF.
A Oxydol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Oxydol 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 Oxydol suppliers with CEP (COS) on PharmaCompass.
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