Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
01 1TRANSO-PHARM HANDELS GMBH Siek DE
02 1Bidachem S.p.A. Fornovo San Giovanni IT
03 1MIDAS PHARMA GMBH Ingelheim am Rhein DE
01 3Crotamiton
01 2Germany
02 1Italy
01 2Valid
02 1Withdrawn by Holder
Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
Certificate Number : CEP 2014-260 - Rev 01
Status : Valid
Issue Date : 2024-11-15
Type : Chemical
Substance Number : 1194
Certificate Number : R1-CEP 1999-131 - Rev 03
Status : Withdrawn by Holder
Issue Date : 2012-05-11
Type : Chemical
Substance Number : 1194
Certificate Number : CEP 2018-095 - Rev 03
Status : Valid
Issue Date : 2024-11-25
Type : Chemical
Substance Number : 1194
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PharmaCompass offers a list of Crotamiton 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 Crotamiton manufacturer or Crotamiton supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Crotamiton manufacturer or Crotamiton supplier.
PharmaCompass also assists you with knowing the Crotamiton API Price utilized in the formulation of products. Crotamiton API Price is not always fixed or binding as the Crotamiton Price is obtained through a variety of data sources. The Crotamiton Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Euraxil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Euraxil, including repackagers and relabelers. The FDA regulates Euraxil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Euraxil 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 Euraxil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Euraxil supplier is an individual or a company that provides Euraxil active pharmaceutical ingredient (API) or Euraxil finished formulations upon request. The Euraxil suppliers may include Euraxil API manufacturers, exporters, distributors and traders.
click here to find a list of Euraxil suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Euraxil CEP of the European Pharmacopoeia monograph is often referred to as a Euraxil Certificate of Suitability (COS). The purpose of a Euraxil CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Euraxil EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Euraxil to their clients by showing that a Euraxil CEP has been issued for it. The manufacturer submits a Euraxil CEP (COS) as part of the market authorization procedure, and it takes on the role of a Euraxil CEP holder for the record. Additionally, the data presented in the Euraxil CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Euraxil DMF.
A Euraxil CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Euraxil 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 Euraxil suppliers with CEP (COS) on PharmaCompass.
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