01 1AbbVie Inc. North Chicago US
02 1AESICA QUEENBOROUGH LIMITED Queenborough GB
03 1SHANDONG NEW TIME PHARMACEUTICAL CO., LTD. Linyi CN
01 3Isoflurane
01 1China
02 1U.S.A
03 1United Kingdom
01 2Valid
02 1Withdrawn by Holder
Certificate Number : R1-CEP 2006-292 - Rev 00
Status : Valid
Issue Date : 2012-09-24
Type : Chemical
Substance Number : 1673
Certificate Number : R1-CEP 2012-280 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2019-04-11
Type : Chemical
Substance Number : 1673
Certificate Number : R1-CEP 2010-078 - Rev 00
Status : Valid
Issue Date : 2016-04-22
Type : Chemical
Substance Number : 1673
A Isoflurane manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Isoflurane, including repackagers and relabelers. The FDA regulates Isoflurane manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Isoflurane 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 Isoflurane manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Isoflurane supplier is an individual or a company that provides Isoflurane active pharmaceutical ingredient (API) or Isoflurane finished formulations upon request. The Isoflurane suppliers may include Isoflurane API manufacturers, exporters, distributors and traders.
click here to find a list of Isoflurane suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Isoflurane CEP of the European Pharmacopoeia monograph is often referred to as a Isoflurane Certificate of Suitability (COS). The purpose of a Isoflurane CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Isoflurane EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Isoflurane to their clients by showing that a Isoflurane CEP has been issued for it. The manufacturer submits a Isoflurane CEP (COS) as part of the market authorization procedure, and it takes on the role of a Isoflurane CEP holder for the record. Additionally, the data presented in the Isoflurane CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Isoflurane DMF.
A Isoflurane CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Isoflurane 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 Isoflurane suppliers with CEP (COS) on PharmaCompass.
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