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