01 1LUKASIEWICZ Research Network-INDUSTRIAL CHEMISTRY INSTITUTE
02 1Nanjing Heron Pharmaceutical Co. , LTD.
03 1Teijin Pharma Limited
01 1Bonn alpha
02 1Tacalcitol
03 1Tacalcitol hydrate
01 1China
02 1Japan
03 1Poland
Registration Number : 306MF10035
Registrant's Address : No. 122 Huakang Road, Jiangbei New Area, Nanjing 211800, China
Initial Date of Registration : 2024-03-06
Latest Date of Registration : 2024-03-06
Registration Number : 218MF10969
Registrant's Address : 8 Rydygiera Str. , 01-793 Warsaw, Poland
Initial Date of Registration : 2006-12-01
Latest Date of Registration : 2009-10-19
Registration Number : 218MF10175
Registrant's Address : 2-1 Kasumigaseki 3-chome, Chiyoda-ku, Tokyo
Initial Date of Registration : 2006-02-08
Latest Date of Registration : 2011-09-28
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PharmaCompass offers a list of Tacalcitol 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 Tacalcitol manufacturer or Tacalcitol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tacalcitol manufacturer or Tacalcitol supplier.
PharmaCompass also assists you with knowing the Tacalcitol API Price utilized in the formulation of products. Tacalcitol API Price is not always fixed or binding as the Tacalcitol Price is obtained through a variety of data sources. The Tacalcitol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bonalfa manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bonalfa, including repackagers and relabelers. The FDA regulates Bonalfa manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bonalfa 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 Bonalfa manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bonalfa supplier is an individual or a company that provides Bonalfa active pharmaceutical ingredient (API) or Bonalfa finished formulations upon request. The Bonalfa suppliers may include Bonalfa API manufacturers, exporters, distributors and traders.
click here to find a list of Bonalfa 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 Bonalfa Drug Master File in Japan (Bonalfa JDMF) empowers Bonalfa 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 Bonalfa JDMF during the approval evaluation for pharmaceutical products. At the time of Bonalfa 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 Bonalfa suppliers with JDMF on PharmaCompass.
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