AMI Lifesciences is Driven by Chemistry. Powered by People.
01 1AMI LIFE SCIENCES PVT. LTD.
02 1Biocon Limited
03 1Cheer Fine Pharmaceutical Co. , Ltd.
04 1DONGBANG FUTURE TECH & LIFE CO. , LTD.
05 1Harman Finochem Ltd.
06 1Honor Lab Limited
07 1Jiangxi Synergy Pharmaceutical Co. , Ltd.
08 1Laurus Labs Limited
09 1Tianjin Minxiang Pharmaceutical Co. , Ltd.
10 1Zhejiang Tianyu Pharmaceutical Co. , Ltd.
AMI Lifesciences is Driven by Chemistry. Powered by People.
Registration Number : 305MF10086
Registrant's Address : 2nd Floor, Prestige Plaza-40, Urmi Society, Near Urmi Cross Road, BPC Road, Akota, Va...
Initial Date of Registration : 2023-07-19
Latest Date of Registration : 2023-07-19
A Vildagliptin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vildagliptin, including repackagers and relabelers. The FDA regulates Vildagliptin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vildagliptin 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 Vildagliptin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vildagliptin supplier is an individual or a company that provides Vildagliptin active pharmaceutical ingredient (API) or Vildagliptin finished formulations upon request. The Vildagliptin suppliers may include Vildagliptin API manufacturers, exporters, distributors and traders.
click here to find a list of Vildagliptin 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 Vildagliptin Drug Master File in Japan (Vildagliptin JDMF) empowers Vildagliptin 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 Vildagliptin JDMF during the approval evaluation for pharmaceutical products. At the time of Vildagliptin 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 Vildagliptin suppliers with JDMF on PharmaCompass.
We have 10 companies offering Vildagliptin
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
