01 1GMT Fine Chemicals SA
02 1Merck & Cie KmG
01 2Calcium folinate
01 2Switzerland
Registration Number : 227MF10147
Registrant's Address : 6, rue des Iles CH-2108 COUVET Switzerland
Initial Date of Registration : 2015-05-20
Latest Date of Registration : 2015-05-20
Registration Number : 218MF10352
Registrant's Address : Weisshausmatte, 6460 Altdorf UR, Switzerland
Initial Date of Registration : 2006-03-17
Latest Date of Registration : 2025-12-11
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PharmaCompass offers a list of Calcium Folinate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Calcium Folinate manufacturer or Calcium Folinate supplier for your needs.
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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.
click here to find a list of Factor, Citrovorum manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
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.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Factor, Citrovorum Drug Master File in Japan (Factor, Citrovorum JDMF) empowers Factor, Citrovorum API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Factor, Citrovorum JDMF during the approval evaluation for pharmaceutical products. At the time of Factor, Citrovorum JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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