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 Bufon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bufon, including repackagers and relabelers. The FDA regulates Bufon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bufon 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 Bufon supplier is an individual or a company that provides Bufon active pharmaceutical ingredient (API) or Bufon finished formulations upon request. The Bufon suppliers may include Bufon API manufacturers, exporters, distributors and traders.
click here to find a list of Bufon suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Bufon CEP of the European Pharmacopoeia monograph is often referred to as a Bufon Certificate of Suitability (COS). The purpose of a Bufon CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Bufon EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Bufon to their clients by showing that a Bufon CEP has been issued for it. The manufacturer submits a Bufon CEP (COS) as part of the market authorization procedure, and it takes on the role of a Bufon CEP holder for the record. Additionally, the data presented in the Bufon CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Bufon DMF.
A Bufon CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Bufon 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 Bufon suppliers with CEP (COS) on PharmaCompass.
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