01 1ScinoPharm Taiwan, Ltd.
01 1Zotarolimus (production only)
01 1Taiwan
Zotarolimus (for manufacturing purposes only)
Registration Number : 219MF10076
Registrant's Address : No. 1, Nan-Ke 8th Road Tainan Science-Based Industrial Park Shan-Hua, Tainan 74144
Initial Date of Registration : 2007-03-14
Latest Date of Registration : 2007-03-14
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PharmaCompass offers a list of Zotarolimus 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 Zotarolimus manufacturer or Zotarolimus supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Zotarolimus manufacturer or Zotarolimus supplier.
PharmaCompass also assists you with knowing the Zotarolimus API Price utilized in the formulation of products. Zotarolimus API Price is not always fixed or binding as the Zotarolimus Price is obtained through a variety of data sources. The Zotarolimus Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zotarolimus manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zotarolimus, including repackagers and relabelers. The FDA regulates Zotarolimus manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zotarolimus API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Zotarolimus supplier is an individual or a company that provides Zotarolimus active pharmaceutical ingredient (API) or Zotarolimus finished formulations upon request. The Zotarolimus suppliers may include Zotarolimus API manufacturers, exporters, distributors and traders.
click here to find a list of Zotarolimus 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 Zotarolimus Drug Master File in Japan (Zotarolimus JDMF) empowers Zotarolimus 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 Zotarolimus JDMF during the approval evaluation for pharmaceutical products. At the time of Zotarolimus 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 Zotarolimus suppliers with JDMF on PharmaCompass.
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