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01 1EDMOND PHARMA S.R.L. Milano IT
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01 1Stanozolol, Micronised
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01 1Italy
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01 1Withdrawn by Holder
Certificate Number : R1-CEP 2002-222 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2011-05-19
Type : Chemical
Substance Number : 1568
60
PharmaCompass offers a list of Stanozolol 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 Stanozolol manufacturer or Stanozolol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Stanozolol manufacturer or Stanozolol supplier.
PharmaCompass also assists you with knowing the Stanozolol API Price utilized in the formulation of products. Stanozolol API Price is not always fixed or binding as the Stanozolol Price is obtained through a variety of data sources. The Stanozolol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Stanozolol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Stanozolol, including repackagers and relabelers. The FDA regulates Stanozolol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Stanozolol 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 Stanozolol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Stanozolol supplier is an individual or a company that provides Stanozolol active pharmaceutical ingredient (API) or Stanozolol finished formulations upon request. The Stanozolol suppliers may include Stanozolol API manufacturers, exporters, distributors and traders.
click here to find a list of Stanozolol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Stanozolol CEP of the European Pharmacopoeia monograph is often referred to as a Stanozolol Certificate of Suitability (COS). The purpose of a Stanozolol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Stanozolol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Stanozolol to their clients by showing that a Stanozolol CEP has been issued for it. The manufacturer submits a Stanozolol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Stanozolol CEP holder for the record. Additionally, the data presented in the Stanozolol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Stanozolol DMF.
A Stanozolol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Stanozolol 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 Stanozolol suppliers with CEP (COS) on PharmaCompass.
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