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01 1ABBOTT MEDICAL St. Paul US
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01 1Glutaraldehyde fixed bovine pericardium
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01 1China
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01 1Valid
Glutaraldehyde Fixed Bovine Pericardium
Certificate Number : CEP 2015-381 - Rev 02
Status : Valid
Issue Date : 2024-08-20
Type : TSE
Substance Number :
40
PharmaCompass offers a list of Glutaraldehyde 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 Glutaraldehyde manufacturer or Glutaraldehyde supplier for your needs.
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PharmaCompass also assists you with knowing the Glutaraldehyde API Price utilized in the formulation of products. Glutaraldehyde API Price is not always fixed or binding as the Glutaraldehyde Price is obtained through a variety of data sources. The Glutaraldehyde Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cidex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cidex, including repackagers and relabelers. The FDA regulates Cidex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cidex API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Cidex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cidex supplier is an individual or a company that provides Cidex active pharmaceutical ingredient (API) or Cidex finished formulations upon request. The Cidex suppliers may include Cidex API manufacturers, exporters, distributors and traders.
click here to find a list of Cidex suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cidex CEP of the European Pharmacopoeia monograph is often referred to as a Cidex Certificate of Suitability (COS). The purpose of a Cidex CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cidex EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cidex to their clients by showing that a Cidex CEP has been issued for it. The manufacturer submits a Cidex CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cidex CEP holder for the record. Additionally, the data presented in the Cidex CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cidex DMF.
A Cidex CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cidex 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 Cidex suppliers with CEP (COS) on PharmaCompass.