Reliable Spanish CDMO Delivering High-Quality APIs and Intermediates with Excellence, Flexibility, and Regulatory Compliance.
01 1KINSY S.L. Murcia ES
01 1Ethacridine lactate monohydrate
01 1Spain
01 1Valid
Reliable Spanish CDMO Delivering High-Quality APIs and Intermediates with Excellence, Flexibility, and Regulatory Compliance.
Reliable Spanish CDMO Delivering High-Quality APIs and Intermediates with Excellence, Flexibility, and Regulatory Compliance.
Ethacridine Lactate Monohydrate
Certificate Number : CEP 2022-246 - Rev 02
Status : Valid
Issue Date : 2024-10-25
Type : Chemical
Substance Number : 1591
28
PharmaCompass offers a list of Ethacridine Lactate 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 Ethacridine Lactate manufacturer or Ethacridine Lactate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ethacridine Lactate manufacturer or Ethacridine Lactate supplier.
PharmaCompass also assists you with knowing the Ethacridine Lactate API Price utilized in the formulation of products. Ethacridine Lactate API Price is not always fixed or binding as the Ethacridine Lactate Price is obtained through a variety of data sources. The Ethacridine Lactate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Rivanol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rivanol, including repackagers and relabelers. The FDA regulates Rivanol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rivanol API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Rivanol supplier is an individual or a company that provides Rivanol active pharmaceutical ingredient (API) or Rivanol finished formulations upon request. The Rivanol suppliers may include Rivanol API manufacturers, exporters, distributors and traders.
click here to find a list of Rivanol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Rivanol CEP of the European Pharmacopoeia monograph is often referred to as a Rivanol Certificate of Suitability (COS). The purpose of a Rivanol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Rivanol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Rivanol to their clients by showing that a Rivanol CEP has been issued for it. The manufacturer submits a Rivanol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Rivanol CEP holder for the record. Additionally, the data presented in the Rivanol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Rivanol DMF.
A Rivanol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Rivanol CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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