01 1ASPEN OSS B.V. Oss NL
02 1VALDEPHARM Val de Reuil FR
01 2Estradiol benzoate
01 1Gabon
02 1Netherlands
01 1Valid
02 1Withdrawn by Holder
Certificate Number : CEP 2012-144 - Rev 02
Status : Valid
Issue Date : 2025-02-10
Type : Chemical
Substance Number : 139
Certificate Number : R1-CEP 2003-001 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2014-01-30
Type : Chemical
Substance Number : 139
87
PharmaCompass offers a list of Estradiol Benzoate 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 Estradiol Benzoate manufacturer or Estradiol Benzoate supplier for your needs.
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PharmaCompass also assists you with knowing the Estradiol Benzoate API Price utilized in the formulation of products. Estradiol Benzoate API Price is not always fixed or binding as the Estradiol Benzoate Price is obtained through a variety of data sources. The Estradiol Benzoate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Oestradiolum benzoylatum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oestradiolum benzoylatum, including repackagers and relabelers. The FDA regulates Oestradiolum benzoylatum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oestradiolum benzoylatum 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 Oestradiolum benzoylatum supplier is an individual or a company that provides Oestradiolum benzoylatum active pharmaceutical ingredient (API) or Oestradiolum benzoylatum finished formulations upon request. The Oestradiolum benzoylatum suppliers may include Oestradiolum benzoylatum API manufacturers, exporters, distributors and traders.
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A Oestradiolum benzoylatum CEP of the European Pharmacopoeia monograph is often referred to as a Oestradiolum benzoylatum Certificate of Suitability (COS). The purpose of a Oestradiolum benzoylatum CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Oestradiolum benzoylatum EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Oestradiolum benzoylatum to their clients by showing that a Oestradiolum benzoylatum CEP has been issued for it. The manufacturer submits a Oestradiolum benzoylatum CEP (COS) as part of the market authorization procedure, and it takes on the role of a Oestradiolum benzoylatum CEP holder for the record. Additionally, the data presented in the Oestradiolum benzoylatum CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Oestradiolum benzoylatum DMF.
A Oestradiolum benzoylatum CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Oestradiolum benzoylatum 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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