01 1DONGBANG FUTURE TECH & LIFE CO. , LTD.
02 1Ryoto Fine Co., Ltd.
01 2Mitiglinide calcium hydrate
01 1Japan
02 1South Korea
Registration Number : 229MF10057
Registrant's Address : 78, Jeyakgongdan 4-gil, Hyangnam-eup, Hwaseong-si, Gyeonggi-do, Korea
Initial Date of Registration : 2017-03-03
Latest Date of Registration : 2017-04-11
Registration Number : 227MF10191
Registrant's Address : 1410 Takada, Kashiwa City, Chiba Prefecture
Initial Date of Registration : 2015-08-03
Latest Date of Registration : 2015-08-03
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PharmaCompass offers a list of Mitiglinide Calcium 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 Mitiglinide Calcium manufacturer or Mitiglinide Calcium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mitiglinide Calcium manufacturer or Mitiglinide Calcium supplier.
A Mitiglinide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mitiglinide, including repackagers and relabelers. The FDA regulates Mitiglinide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mitiglinide 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 Mitiglinide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Mitiglinide supplier is an individual or a company that provides Mitiglinide active pharmaceutical ingredient (API) or Mitiglinide finished formulations upon request. The Mitiglinide suppliers may include Mitiglinide API manufacturers, exporters, distributors and traders.
click here to find a list of Mitiglinide 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 Mitiglinide Drug Master File in Japan (Mitiglinide JDMF) empowers Mitiglinide 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 Mitiglinide JDMF during the approval evaluation for pharmaceutical products. At the time of Mitiglinide 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 Mitiglinide suppliers with JDMF on PharmaCompass.
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