01 1KYOWA PHARMA CHEMICAL CO., LTD. Takaoka JP
01 1Dinoprostone
01 1Japan
01 1Valid
Certificate Number : CEP 2003-029 - Rev 03
Status : Valid
Issue Date : 2025-02-18
Type : Chemical
Substance Number : 1311
91
PharmaCompass offers a list of Dinoprostone 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 Dinoprostone manufacturer or Dinoprostone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dinoprostone manufacturer or Dinoprostone supplier.
PharmaCompass also assists you with knowing the Dinoprostone API Price utilized in the formulation of products. Dinoprostone API Price is not always fixed or binding as the Dinoprostone Price is obtained through a variety of data sources. The Dinoprostone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Prostin E2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prostin E2, including repackagers and relabelers. The FDA regulates Prostin E2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prostin E2 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 Prostin E2 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Prostin E2 supplier is an individual or a company that provides Prostin E2 active pharmaceutical ingredient (API) or Prostin E2 finished formulations upon request. The Prostin E2 suppliers may include Prostin E2 API manufacturers, exporters, distributors and traders.
click here to find a list of Prostin E2 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Prostin E2 CEP of the European Pharmacopoeia monograph is often referred to as a Prostin E2 Certificate of Suitability (COS). The purpose of a Prostin E2 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Prostin E2 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Prostin E2 to their clients by showing that a Prostin E2 CEP has been issued for it. The manufacturer submits a Prostin E2 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Prostin E2 CEP holder for the record. Additionally, the data presented in the Prostin E2 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Prostin E2 DMF.
A Prostin E2 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Prostin E2 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 Prostin E2 suppliers with CEP (COS) on PharmaCompass.
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