01 1Laboratorios Beta S.A. Buenos Aires AR
02 1N.V. ORGANON Oss NL
03 2Novo Nordisk A/S Bagsvaerd DK
04 1Novo Nordisk Produção Farmacêutica do Brasil Ltda Montes Claros BR
01 3Insulin, bovine
02 1Insulin, bovine, "chromatographed"
03 1Insulin, bovine, "monocomponent"
01 1Argentina
02 1Brazil
03 2Denmark
04 1U.S.A
01 2Valid
02 3Withdrawn by Holder
Certificate Number : R1-CEP 2005-214 - Rev 00
Status : Valid
Issue Date : 2011-01-07
Type : TSE
Substance Number :
Certificate Number : R1-CEP 2000-230 - Rev 00
Status : Valid
Issue Date : 2006-05-17
Type : TSE
Substance Number :
Insulin, Bovine, "monocomponent"
Certificate Number : R0-CEP 2000-135 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2005-03-08
Type : TSE
Substance Number :
Insulin, Bovine, "chromatographed"
Certificate Number : R0-CEP 2000-340 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2005-03-08
Type : TSE
Substance Number :
Certificate Number : R1-CEP 2000-156 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2007-03-06
Type : TSE
Substance Number :
16
PharmaCompass offers a list of Bovine Insulin 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 Bovine Insulin manufacturer or Bovine Insulin supplier for your needs.
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PharmaCompass also assists you with knowing the Bovine Insulin API Price utilized in the formulation of products. Bovine Insulin API Price is not always fixed or binding as the Bovine Insulin Price is obtained through a variety of data sources. The Bovine Insulin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A INSULIN RECOMBINANT HUMAN manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of INSULIN RECOMBINANT HUMAN, including repackagers and relabelers. The FDA regulates INSULIN RECOMBINANT HUMAN manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. INSULIN RECOMBINANT HUMAN 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 INSULIN RECOMBINANT HUMAN supplier is an individual or a company that provides INSULIN RECOMBINANT HUMAN active pharmaceutical ingredient (API) or INSULIN RECOMBINANT HUMAN finished formulations upon request. The INSULIN RECOMBINANT HUMAN suppliers may include INSULIN RECOMBINANT HUMAN API manufacturers, exporters, distributors and traders.
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A INSULIN RECOMBINANT HUMAN CEP of the European Pharmacopoeia monograph is often referred to as a INSULIN RECOMBINANT HUMAN Certificate of Suitability (COS). The purpose of a INSULIN RECOMBINANT HUMAN CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of INSULIN RECOMBINANT HUMAN EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of INSULIN RECOMBINANT HUMAN to their clients by showing that a INSULIN RECOMBINANT HUMAN CEP has been issued for it. The manufacturer submits a INSULIN RECOMBINANT HUMAN CEP (COS) as part of the market authorization procedure, and it takes on the role of a INSULIN RECOMBINANT HUMAN CEP holder for the record. Additionally, the data presented in the INSULIN RECOMBINANT HUMAN CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the INSULIN RECOMBINANT HUMAN DMF.
A INSULIN RECOMBINANT HUMAN CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. INSULIN RECOMBINANT HUMAN 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 INSULIN RECOMBINANT HUMAN suppliers with CEP (COS) on PharmaCompass.
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