01 1Vifor (International) Inc.
01 1Carboxymethyl maltose ferric
01 1Switzerland
Registration Number : 229MF10211
Registrant's Address : Rechenstrasse 37, CH-9001 St. Gallen
Initial Date of Registration : 2017-12-01
Latest Date of Registration : 2023-10-04
13
PharmaCompass offers a list of Ferric Carboxymaltose 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 Ferric Carboxymaltose manufacturer or Ferric Carboxymaltose supplier for your needs.
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PharmaCompass also assists you with knowing the Ferric Carboxymaltose API Price utilized in the formulation of products. Ferric Carboxymaltose API Price is not always fixed or binding as the Ferric Carboxymaltose Price is obtained through a variety of data sources. The Ferric Carboxymaltose Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Injectafer manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Injectafer, including repackagers and relabelers. The FDA regulates Injectafer manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Injectafer 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 Injectafer supplier is an individual or a company that provides Injectafer active pharmaceutical ingredient (API) or Injectafer finished formulations upon request. The Injectafer suppliers may include Injectafer API manufacturers, exporters, distributors and traders.
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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 Injectafer Drug Master File in Japan (Injectafer JDMF) empowers Injectafer 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 Injectafer JDMF during the approval evaluation for pharmaceutical products. At the time of Injectafer 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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