01 1Hebei Shengxue Dacheng Pharmaceutical Co. , Ltd.
01 1Streptomycin sulfate
01 1China
Registration Number : 229MF10076
Registrant's Address : No. 50 Shengxue Road, Luancheng Shijiazhuang, Hebei Province, China
Initial Date of Registration : 2017-04-11
Latest Date of Registration : 2017-04-11
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A Strepto Fatol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Strepto Fatol, including repackagers and relabelers. The FDA regulates Strepto Fatol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Strepto Fatol 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 Strepto Fatol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Strepto Fatol supplier is an individual or a company that provides Strepto Fatol active pharmaceutical ingredient (API) or Strepto Fatol finished formulations upon request. The Strepto Fatol suppliers may include Strepto Fatol API manufacturers, exporters, distributors and traders.
click here to find a list of Strepto Fatol 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 Strepto Fatol Drug Master File in Japan (Strepto Fatol JDMF) empowers Strepto Fatol 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 Strepto Fatol JDMF during the approval evaluation for pharmaceutical products. At the time of Strepto Fatol 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 Strepto Fatol suppliers with JDMF on PharmaCompass.
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