01 1MITSUBISHI CHEMICAL CORPORATION Chiyoda JP
02 1MITSUBISHI CHEMICAL CORPORATION Tokyo JP
01 1Poly(vinyl alcohol), Viscosity 42.5 mPa･s, Ester Value 147 mg KOH/g, Process 2
02 1Poly(vinyl alcohol), Viscosity 5.1 mPa.s, Ester value 140 mg KOH/g
01 2Japan
01 2Valid
Poly(vinyl Alcohol), Viscosity 5.1 MPa.s, Ester ...
Certificate Number : R1-CEP 2013-209 - Rev 00
Status : Valid
Issue Date : 2021-09-28
Type : Chemical
Substance Number : 1961
Poly(vinyl Alcohol), Viscosity 42.5 MPa･s, Est...
Certificate Number : CEP 2022-281 - Rev 02
Status : Valid
Issue Date : 2024-06-26
Type : Chemical
Substance Number : 1961
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PharmaCompass offers a list of Polyvinyl Alcohol API 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 Polyvinyl Alcohol API manufacturer or Polyvinyl Alcohol API supplier for your needs.
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A Hydroxyethene manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydroxyethene, including repackagers and relabelers. The FDA regulates Hydroxyethene manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydroxyethene 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 Hydroxyethene supplier is an individual or a company that provides Hydroxyethene active pharmaceutical ingredient (API) or Hydroxyethene finished formulations upon request. The Hydroxyethene suppliers may include Hydroxyethene API manufacturers, exporters, distributors and traders.
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A Hydroxyethene CEP of the European Pharmacopoeia monograph is often referred to as a Hydroxyethene Certificate of Suitability (COS). The purpose of a Hydroxyethene CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Hydroxyethene EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Hydroxyethene to their clients by showing that a Hydroxyethene CEP has been issued for it. The manufacturer submits a Hydroxyethene CEP (COS) as part of the market authorization procedure, and it takes on the role of a Hydroxyethene CEP holder for the record. Additionally, the data presented in the Hydroxyethene CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Hydroxyethene DMF.
A Hydroxyethene CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Hydroxyethene 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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