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
A Tacalcitol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tacalcitol, including repackagers and relabelers. The FDA regulates Tacalcitol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tacalcitol 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 Tacalcitol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tacalcitol supplier is an individual or a company that provides Tacalcitol active pharmaceutical ingredient (API) or Tacalcitol finished formulations upon request. The Tacalcitol suppliers may include Tacalcitol API manufacturers, exporters, distributors and traders.
click here to find a list of Tacalcitol 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 Tacalcitol Drug Master File in Japan (Tacalcitol JDMF) empowers Tacalcitol 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 Tacalcitol JDMF during the approval evaluation for pharmaceutical products. At the time of Tacalcitol 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 Tacalcitol suppliers with JDMF on PharmaCompass.
We have 3 companies offering Tacalcitol
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
