01 1HEC PHARM CO. ,LTD
01 1Erythromycin thiocyanate
01 1China
Registration Number : 228MF10168
Registrant's Address : No. 62 Binjiang Road, Yidu, Hubei Province, P. R. China
Initial Date of Registration : 2016-08-19
Latest Date of Registration : 2021-10-07
A Erythromycin Thiocyanate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Erythromycin Thiocyanate, including repackagers and relabelers. The FDA regulates Erythromycin Thiocyanate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Erythromycin Thiocyanate 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 Erythromycin Thiocyanate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Erythromycin Thiocyanate supplier is an individual or a company that provides Erythromycin Thiocyanate active pharmaceutical ingredient (API) or Erythromycin Thiocyanate finished formulations upon request. The Erythromycin Thiocyanate suppliers may include Erythromycin Thiocyanate API manufacturers, exporters, distributors and traders.
click here to find a list of Erythromycin Thiocyanate 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 Erythromycin Thiocyanate Drug Master File in Japan (Erythromycin Thiocyanate JDMF) empowers Erythromycin Thiocyanate 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 Erythromycin Thiocyanate JDMF during the approval evaluation for pharmaceutical products. At the time of Erythromycin Thiocyanate 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 Erythromycin Thiocyanate suppliers with JDMF on PharmaCompass.
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