01 1Southwest Synthetic Pharmaceutical Corp. , Ltd.
01 1Sulfadiazine
01 1China
Registration Number : 228MF10135
Registrant's Address : NO. 22, Founder Avenue, Shuitu Township, Beibei District, Chongqing 400714, P. R. Chi...
Initial Date of Registration : 2016-07-27
Latest Date of Registration : 2016-07-27
A Diazin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diazin, including repackagers and relabelers. The FDA regulates Diazin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diazin 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 Diazin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diazin supplier is an individual or a company that provides Diazin active pharmaceutical ingredient (API) or Diazin finished formulations upon request. The Diazin suppliers may include Diazin API manufacturers, exporters, distributors and traders.
click here to find a list of Diazin 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 Diazin Drug Master File in Japan (Diazin JDMF) empowers Diazin 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 Diazin JDMF during the approval evaluation for pharmaceutical products. At the time of Diazin 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 Diazin suppliers with JDMF on PharmaCompass.
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