01 1ScinoPharm Taiwan, Ltd.
01 1Exemestane
01 1Taiwan
Registration Number : 222MF10188
Registrant's Address : No. 1, Nan-Ke 8th Road, Shan-Hua, Tainan 74144, Taiwan
Initial Date of Registration : 2010-07-02
Latest Date of Registration : 2020-11-18
85
PharmaCompass offers a list of Exemestane 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 Exemestane manufacturer or Exemestane supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Exemestane manufacturer or Exemestane supplier.
PharmaCompass also assists you with knowing the Exemestane API Price utilized in the formulation of products. Exemestane API Price is not always fixed or binding as the Exemestane Price is obtained through a variety of data sources. The Exemestane Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Exemestano manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Exemestano, including repackagers and relabelers. The FDA regulates Exemestano manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Exemestano 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 Exemestano manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Exemestano supplier is an individual or a company that provides Exemestano active pharmaceutical ingredient (API) or Exemestano finished formulations upon request. The Exemestano suppliers may include Exemestano API manufacturers, exporters, distributors and traders.
click here to find a list of Exemestano 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 Exemestano Drug Master File in Japan (Exemestano JDMF) empowers Exemestano 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 Exemestano JDMF during the approval evaluation for pharmaceutical products. At the time of Exemestano 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 Exemestano suppliers with JDMF on PharmaCompass.
We have 1 companies offering Exemestano
Get in contact with the supplier of your choice:
