01 1GMT FINE CHEMICALS S.A. Couvet CH
02 1HUZHOU ZHANWANG PHARMACEUTICAL CO., LTD. Linghu Town CN
03 1MERCK & CIE KMG Schaffhausen CH
01 3Calcium folinate hydrate
01 1China
02 2Switzerland
01 3Valid
Certificate Number : CEP 2004-009 - Rev 04
Status : Valid
Issue Date : 2024-04-15
Type : Chemical
Substance Number : 978
Certificate Number : R1-CEP 2011-370 - Rev 00
Status : Valid
Issue Date : 2019-07-26
Type : Chemical
Substance Number : 978
Certificate Number : R1-CEP 1996-055 - Rev 08
Status : Valid
Issue Date : 2023-05-19
Type : Chemical
Substance Number : 978
41
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A Factor, Citrovorum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Factor, Citrovorum, including repackagers and relabelers. The FDA regulates Factor, Citrovorum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Factor, Citrovorum 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 Factor, Citrovorum supplier is an individual or a company that provides Factor, Citrovorum active pharmaceutical ingredient (API) or Factor, Citrovorum finished formulations upon request. The Factor, Citrovorum suppliers may include Factor, Citrovorum API manufacturers, exporters, distributors and traders.
click here to find a list of Factor, Citrovorum suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Factor, Citrovorum CEP of the European Pharmacopoeia monograph is often referred to as a Factor, Citrovorum Certificate of Suitability (COS). The purpose of a Factor, Citrovorum CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Factor, Citrovorum EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Factor, Citrovorum to their clients by showing that a Factor, Citrovorum CEP has been issued for it. The manufacturer submits a Factor, Citrovorum CEP (COS) as part of the market authorization procedure, and it takes on the role of a Factor, Citrovorum CEP holder for the record. Additionally, the data presented in the Factor, Citrovorum CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Factor, Citrovorum DMF.
A Factor, Citrovorum CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Factor, Citrovorum 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 Factor, Citrovorum suppliers with CEP (COS) on PharmaCompass.
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