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
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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 EXM manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EXM, including repackagers and relabelers. The FDA regulates EXM manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EXM 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 EXM manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A EXM supplier is an individual or a company that provides EXM active pharmaceutical ingredient (API) or EXM finished formulations upon request. The EXM suppliers may include EXM API manufacturers, exporters, distributors and traders.
click here to find a list of EXM 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 EXM Drug Master File in Japan (EXM JDMF) empowers EXM 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 EXM JDMF during the approval evaluation for pharmaceutical products. At the time of EXM 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 EXM suppliers with JDMF on PharmaCompass.
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