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