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01 KATWIJK CHEMIE BV Katwijk ZH NL (1)
01 Deferiprone (1)
01 Netherlands (1)
01 Valid (1)
56
PharmaCompass offers a list of Deferiprone 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 Deferiprone manufacturer or Deferiprone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Deferiprone manufacturer or Deferiprone supplier.
PharmaCompass also assists you with knowing the Deferiprone API Price utilized in the formulation of products. Deferiprone API Price is not always fixed or binding as the Deferiprone Price is obtained through a variety of data sources. The Deferiprone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Deferiprone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Deferiprone, including repackagers and relabelers. The FDA regulates Deferiprone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Deferiprone 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 Deferiprone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Deferiprone supplier is an individual or a company that provides Deferiprone active pharmaceutical ingredient (API) or Deferiprone finished formulations upon request. The Deferiprone suppliers may include Deferiprone API manufacturers, exporters, distributors and traders.
click here to find a list of Deferiprone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Deferiprone CEP of the European Pharmacopoeia monograph is often referred to as a Deferiprone Certificate of Suitability (COS). The purpose of a Deferiprone CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Deferiprone EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Deferiprone to their clients by showing that a Deferiprone CEP has been issued for it. The manufacturer submits a Deferiprone CEP (COS) as part of the market authorization procedure, and it takes on the role of a Deferiprone CEP holder for the record. Additionally, the data presented in the Deferiprone CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Deferiprone DMF.
A Deferiprone CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Deferiprone 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 Deferiprone suppliers with CEP (COS) on PharmaCompass.
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