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01 1LINNEA S.A. Riazzino CH
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01 1Vincamine
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01 1Switzerland
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01 1Valid
Certificate Number : CEP 2022-273 - Rev 00
Status : Valid
Issue Date : 2024-06-25
Type : Chemical
Substance Number : 1800
36
PharmaCompass offers a list of Vincamine 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 Vincamine manufacturer or Vincamine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vincamine manufacturer or Vincamine supplier.
PharmaCompass also assists you with knowing the Vincamine API Price utilized in the formulation of products. Vincamine API Price is not always fixed or binding as the Vincamine Price is obtained through a variety of data sources. The Vincamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Monorin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Monorin, including repackagers and relabelers. The FDA regulates Monorin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Monorin 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 Monorin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Monorin supplier is an individual or a company that provides Monorin active pharmaceutical ingredient (API) or Monorin finished formulations upon request. The Monorin suppliers may include Monorin API manufacturers, exporters, distributors and traders.
click here to find a list of Monorin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Monorin CEP of the European Pharmacopoeia monograph is often referred to as a Monorin Certificate of Suitability (COS). The purpose of a Monorin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Monorin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Monorin to their clients by showing that a Monorin CEP has been issued for it. The manufacturer submits a Monorin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Monorin CEP holder for the record. Additionally, the data presented in the Monorin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Monorin DMF.
A Monorin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Monorin 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 Monorin suppliers with CEP (COS) on PharmaCompass.