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