01 1BrightGene Pharmaceutical Co. , Ltd.
01 1Everolimus
01 1China
Registration Number : 230MF10023
Registrant's Address : Building C25-C28, No. 218 Xinghu Road, Suzhou Industrial Park, Suzhou, Jiangsu, China...
Initial Date of Registration : 2018-02-14
Latest Date of Registration : 2018-10-23
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PharmaCompass offers a list of Everolimus 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 Everolimus manufacturer or Everolimus supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Everolimus manufacturer or Everolimus supplier.
PharmaCompass also assists you with knowing the Everolimus API Price utilized in the formulation of products. Everolimus API Price is not always fixed or binding as the Everolimus Price is obtained through a variety of data sources. The Everolimus Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zortress manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zortress, including repackagers and relabelers. The FDA regulates Zortress manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zortress 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 Zortress manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zortress supplier is an individual or a company that provides Zortress active pharmaceutical ingredient (API) or Zortress finished formulations upon request. The Zortress suppliers may include Zortress API manufacturers, exporters, distributors and traders.
click here to find a list of Zortress 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 Zortress Drug Master File in Japan (Zortress JDMF) empowers Zortress 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 Zortress JDMF during the approval evaluation for pharmaceutical products. At the time of Zortress 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 Zortress suppliers with JDMF on PharmaCompass.
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