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 PGE2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PGE2, including repackagers and relabelers. The FDA regulates PGE2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PGE2 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 PGE2 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A PGE2 supplier is an individual or a company that provides PGE2 active pharmaceutical ingredient (API) or PGE2 finished formulations upon request. The PGE2 suppliers may include PGE2 API manufacturers, exporters, distributors and traders.
click here to find a list of PGE2 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A PGE2 CEP of the European Pharmacopoeia monograph is often referred to as a PGE2 Certificate of Suitability (COS). The purpose of a PGE2 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of PGE2 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of PGE2 to their clients by showing that a PGE2 CEP has been issued for it. The manufacturer submits a PGE2 CEP (COS) as part of the market authorization procedure, and it takes on the role of a PGE2 CEP holder for the record. Additionally, the data presented in the PGE2 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the PGE2 DMF.
A PGE2 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. PGE2 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 PGE2 suppliers with CEP (COS) on PharmaCompass.
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