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01 1KYOWA PHARMA CHEMICAL CO., LTD. Takaoka JP
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01 1Dinoprostone
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01 1Japan
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01 1Valid
Certificate Number : CEP 2003-029 - Rev 03
Status : Valid
Issue Date : 2025-02-18
Type : Chemical
Substance Number : 1311
61
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 P2E manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of P2E, including repackagers and relabelers. The FDA regulates P2E manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. P2E 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 P2E manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A P2E supplier is an individual or a company that provides P2E active pharmaceutical ingredient (API) or P2E finished formulations upon request. The P2E suppliers may include P2E API manufacturers, exporters, distributors and traders.
click here to find a list of P2E suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A P2E CEP of the European Pharmacopoeia monograph is often referred to as a P2E Certificate of Suitability (COS). The purpose of a P2E CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of P2E EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of P2E to their clients by showing that a P2E CEP has been issued for it. The manufacturer submits a P2E CEP (COS) as part of the market authorization procedure, and it takes on the role of a P2E CEP holder for the record. Additionally, the data presented in the P2E CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the P2E DMF.
A P2E CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. P2E 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 P2E suppliers with CEP (COS) on PharmaCompass.
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