01 1A&C AMERICAN CHEMICALS LTD. Montreal CA
02 1BASF SE Ludwigshafen DE
03 1ICN POLFA RZESZOW S.A. Rzeszow PL
01 3Phenoxyethanol
01 1Germany
02 1Poland
03 1U.S.A
01 3Valid
Certificate Number : CEP 2016-213 - Rev 02
Status : Valid
Issue Date : 2024-01-19
Type : Chemical
Substance Number : 781
Certificate Number : R0-CEP 2021-489 - Rev 00
Status : Valid
Issue Date : 2022-08-16
Type : Chemical
Substance Number : 781
Certificate Number : CEP 2023-276 - Rev 00
Status : Valid
Issue Date : 2024-05-06
Type : Chemical
Substance Number : 781
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PharmaCompass offers a list of 2-Phenoxyethanol 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 2-Phenoxyethanol manufacturer or 2-Phenoxyethanol supplier for your needs.
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A Tox21_300842 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300842, including repackagers and relabelers. The FDA regulates Tox21_300842 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300842 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Tox21_300842 supplier is an individual or a company that provides Tox21_300842 active pharmaceutical ingredient (API) or Tox21_300842 finished formulations upon request. The Tox21_300842 suppliers may include Tox21_300842 API manufacturers, exporters, distributors and traders.
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A Tox21_300842 CEP of the European Pharmacopoeia monograph is often referred to as a Tox21_300842 Certificate of Suitability (COS). The purpose of a Tox21_300842 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tox21_300842 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tox21_300842 to their clients by showing that a Tox21_300842 CEP has been issued for it. The manufacturer submits a Tox21_300842 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tox21_300842 CEP holder for the record. Additionally, the data presented in the Tox21_300842 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tox21_300842 DMF.
A Tox21_300842 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tox21_300842 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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