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01 1SANOFI WINTHROP INDUSTRIE
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01 1Hydroxocobalamin
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01 1France
Registration Number : 226MF10198
Registrant's Address : 82 Avenue Raspail 94250 Gentilly France
Initial Date of Registration : 2014-10-27
Latest Date of Registration : 2016-01-08
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PharmaCompass offers a list of Hydroxocobalamin 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 Hydroxocobalamin manufacturer or Hydroxocobalamin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydroxocobalamin manufacturer or Hydroxocobalamin supplier.
PharmaCompass also assists you with knowing the Hydroxocobalamin API Price utilized in the formulation of products. Hydroxocobalamin API Price is not always fixed or binding as the Hydroxocobalamin Price is obtained through a variety of data sources. The Hydroxocobalamin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cyanokit manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cyanokit, including repackagers and relabelers. The FDA regulates Cyanokit manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cyanokit 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 Cyanokit manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cyanokit supplier is an individual or a company that provides Cyanokit active pharmaceutical ingredient (API) or Cyanokit finished formulations upon request. The Cyanokit suppliers may include Cyanokit API manufacturers, exporters, distributors and traders.
click here to find a list of Cyanokit suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 Cyanokit Drug Master File in Japan (Cyanokit JDMF) empowers Cyanokit 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 Cyanokit JDMF during the approval evaluation for pharmaceutical products. At the time of Cyanokit JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Cyanokit suppliers with JDMF on PharmaCompass.