01 1BAYER AG Leverkusen DE
02 1STEROID S.P.A. Cologno Monzese IT
01 2Testosterone enantate
01 1Germany
02 1Italy
01 2Valid
Certificate Number : R1-CEP 2001-155 - Rev 03
Status : Valid
Issue Date : 2021-09-24
Type : Chemical
Substance Number : 1048
Certificate Number : R1-CEP 2012-306 - Rev 00
Status : Valid
Issue Date : 2019-03-15
Type : Chemical
Substance Number : 1048
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PharmaCompass offers a list of Testosterone Enanthate 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 Testosterone Enanthate manufacturer or Testosterone Enanthate supplier for your needs.
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PharmaCompass also assists you with knowing the Testosterone Enanthate API Price utilized in the formulation of products. Testosterone Enanthate API Price is not always fixed or binding as the Testosterone Enanthate Price is obtained through a variety of data sources. The Testosterone Enanthate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Primoteston Depot manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Primoteston Depot, including repackagers and relabelers. The FDA regulates Primoteston Depot manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Primoteston Depot 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 Primoteston Depot supplier is an individual or a company that provides Primoteston Depot active pharmaceutical ingredient (API) or Primoteston Depot finished formulations upon request. The Primoteston Depot suppliers may include Primoteston Depot API manufacturers, exporters, distributors and traders.
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A Primoteston Depot CEP of the European Pharmacopoeia monograph is often referred to as a Primoteston Depot Certificate of Suitability (COS). The purpose of a Primoteston Depot CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Primoteston Depot EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Primoteston Depot to their clients by showing that a Primoteston Depot CEP has been issued for it. The manufacturer submits a Primoteston Depot CEP (COS) as part of the market authorization procedure, and it takes on the role of a Primoteston Depot CEP holder for the record. Additionally, the data presented in the Primoteston Depot CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Primoteston Depot DMF.
A Primoteston Depot CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Primoteston Depot 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 Primoteston Depot suppliers with CEP (COS) on PharmaCompass.
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