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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PharmaCompass also assists you with knowing the Polyvinyl Alcohol API API Price utilized in the formulation of products. Polyvinyl Alcohol API API Price is not always fixed or binding as the Polyvinyl Alcohol API Price is obtained through a variety of data sources. The Polyvinyl Alcohol API Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vinol 125 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vinol 125, including repackagers and relabelers. The FDA regulates Vinol 125 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vinol 125 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 Vinol 125 supplier is an individual or a company that provides Vinol 125 active pharmaceutical ingredient (API) or Vinol 125 finished formulations upon request. The Vinol 125 suppliers may include Vinol 125 API manufacturers, exporters, distributors and traders.
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A Vinol 125 CEP of the European Pharmacopoeia monograph is often referred to as a Vinol 125 Certificate of Suitability (COS). The purpose of a Vinol 125 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Vinol 125 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Vinol 125 to their clients by showing that a Vinol 125 CEP has been issued for it. The manufacturer submits a Vinol 125 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Vinol 125 CEP holder for the record. Additionally, the data presented in the Vinol 125 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Vinol 125 DMF.
A Vinol 125 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Vinol 125 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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