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01 1Becton, Dickinson and Company Sparks US
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01 1Trypticase Soy Agar with Lecithin and Polysorbate 80, Product codes: 221961, 222208, 221238, 222207, 221287, 292480, 292270, 292488, 292335, 299896, 292649, 292650, 292425, 221288, 215276, 215338, 215341, 215342, 215345 and 215414
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01 1U.S.A
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01 1Valid
Trypticase Soy Agar With Lecithin And Polysorbat...
Certificate Number : R1-CEP 2000-382 - Rev 06
Status : Valid
Issue Date : 2018-10-26
Type : TSE
Substance Number :
41
PharmaCompass offers a list of Polysorbate API 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 Polysorbate API manufacturer or Polysorbate API supplier for your needs.
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PharmaCompass also assists you with knowing the Polysorbate API API Price utilized in the formulation of products. Polysorbate API API Price is not always fixed or binding as the Polysorbate API Price is obtained through a variety of data sources. The Polysorbate API Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tween 20 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tween 20, including repackagers and relabelers. The FDA regulates Tween 20 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tween 20 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 Tween 20 supplier is an individual or a company that provides Tween 20 active pharmaceutical ingredient (API) or Tween 20 finished formulations upon request. The Tween 20 suppliers may include Tween 20 API manufacturers, exporters, distributors and traders.
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A Tween 20 CEP of the European Pharmacopoeia monograph is often referred to as a Tween 20 Certificate of Suitability (COS). The purpose of a Tween 20 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tween 20 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tween 20 to their clients by showing that a Tween 20 CEP has been issued for it. The manufacturer submits a Tween 20 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tween 20 CEP holder for the record. Additionally, the data presented in the Tween 20 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tween 20 DMF.
A Tween 20 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tween 20 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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