01 1Ashland Industries Europe GmbH Schaffhausen CH
02 1Croda Europe Limited Leek GB
01 1Omega-3-acid triglycerides, Grade SF07400
02 1Povidone, Grades C-12, C-17, C-30, K-12, K-17, K-25, K-29/32
01 1Switzerland
02 1United Kingdom
01 2Valid
Povidone, Grades C-12, C-17, C-30, K-12, K-17, K...
Certificate Number : R1-CEP 2004-291 - Rev 00
Status : Valid
Issue Date : 2014-06-23
Type : Chemical
Substance Number : 685
Omega-3-acid Triglycerides, Grade SF07400
Certificate Number : R1-CEP 2005-265 - Rev 00
Status : Valid
Issue Date : 2014-09-04
Type : Chemical
Substance Number : 1352
73
PharmaCompass offers a list of Diethylstilbestrol 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 Diethylstilbestrol manufacturer or Diethylstilbestrol supplier for your needs.
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PharmaCompass also assists you with knowing the Diethylstilbestrol API Price utilized in the formulation of products. Diethylstilbestrol API Price is not always fixed or binding as the Diethylstilbestrol Price is obtained through a variety of data sources. The Diethylstilbestrol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A OeKolp manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of OeKolp, including repackagers and relabelers. The FDA regulates OeKolp manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. OeKolp API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A OeKolp supplier is an individual or a company that provides OeKolp active pharmaceutical ingredient (API) or OeKolp finished formulations upon request. The OeKolp suppliers may include OeKolp API manufacturers, exporters, distributors and traders.
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A OeKolp CEP of the European Pharmacopoeia monograph is often referred to as a OeKolp Certificate of Suitability (COS). The purpose of a OeKolp CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of OeKolp EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of OeKolp to their clients by showing that a OeKolp CEP has been issued for it. The manufacturer submits a OeKolp CEP (COS) as part of the market authorization procedure, and it takes on the role of a OeKolp CEP holder for the record. Additionally, the data presented in the OeKolp CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the OeKolp DMF.
A OeKolp CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. OeKolp 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 OeKolp suppliers with CEP (COS) on PharmaCompass.
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