01 1Liaoning Beiqi Pharmaceutical Co. , Ltd.
01 1Ethionamide
01 1China
Registration Number : 221MF10259
Registrant's Address : No. 18-6, Huanghai Street, Zhenxing District, Dandong City, China
Initial Date of Registration : 2009-12-03
Latest Date of Registration : 2009-12-03
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PharmaCompass offers a list of Ethionamide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Ethionamide manufacturer or Ethionamide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ethionamide manufacturer or Ethionamide supplier.
PharmaCompass also assists you with knowing the Ethionamide API Price utilized in the formulation of products. Ethionamide API Price is not always fixed or binding as the Ethionamide Price is obtained through a variety of data sources. The Ethionamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Aetiva manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aetiva, including repackagers and relabelers. The FDA regulates Aetiva manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aetiva 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 Aetiva manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aetiva supplier is an individual or a company that provides Aetiva active pharmaceutical ingredient (API) or Aetiva finished formulations upon request. The Aetiva suppliers may include Aetiva API manufacturers, exporters, distributors and traders.
click here to find a list of Aetiva 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 Aetiva Drug Master File in Japan (Aetiva JDMF) empowers Aetiva 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 Aetiva JDMF during the approval evaluation for pharmaceutical products. At the time of Aetiva 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 Aetiva suppliers with JDMF on PharmaCompass.
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