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.
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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 6-methylideneandrosta-1,4-diene-3,17-dione manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 6-methylideneandrosta-1,4-diene-3,17-dione, including repackagers and relabelers. The FDA regulates 6-methylideneandrosta-1,4-diene-3,17-dione manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 6-methylideneandrosta-1,4-diene-3,17-dione API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A 6-methylideneandrosta-1,4-diene-3,17-dione supplier is an individual or a company that provides 6-methylideneandrosta-1,4-diene-3,17-dione active pharmaceutical ingredient (API) or 6-methylideneandrosta-1,4-diene-3,17-dione finished formulations upon request. The 6-methylideneandrosta-1,4-diene-3,17-dione suppliers may include 6-methylideneandrosta-1,4-diene-3,17-dione API manufacturers, exporters, distributors and traders.
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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 6-methylideneandrosta-1,4-diene-3,17-dione Drug Master File in Japan (6-methylideneandrosta-1,4-diene-3,17-dione JDMF) empowers 6-methylideneandrosta-1,4-diene-3,17-dione 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 6-methylideneandrosta-1,4-diene-3,17-dione JDMF during the approval evaluation for pharmaceutical products. At the time of 6-methylideneandrosta-1,4-diene-3,17-dione JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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We have 1 companies offering 6-methylideneandrosta-1,4-diene-3,17-dione
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