01 1INDUSTRIALE CHIMICA s. r. l.
02 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
01 2Fulvestrant
01 2Italy
Registration Number : 303MF10021
Registrant's Address : Via E. H. Grieg, 13, 21047 Saronno (VARESE) ITALY
Initial Date of Registration : 2021-01-28
Latest Date of Registration : 2023-11-15
Registration Number : 303MF10127
Registrant's Address : Piazzale Luigi Cadorna, 4 - 20123 MILANO, Italy
Initial Date of Registration : 2021-08-16
Latest Date of Registration : 2021-08-16
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PharmaCompass offers a list of Fulvestrant 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 Fulvestrant manufacturer or Fulvestrant supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fulvestrant manufacturer or Fulvestrant supplier.
PharmaCompass also assists you with knowing the Fulvestrant API Price utilized in the formulation of products. Fulvestrant API Price is not always fixed or binding as the Fulvestrant Price is obtained through a variety of data sources. The Fulvestrant Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fulvestrant manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fulvestrant, including repackagers and relabelers. The FDA regulates Fulvestrant manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fulvestrant 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 Fulvestrant manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fulvestrant supplier is an individual or a company that provides Fulvestrant active pharmaceutical ingredient (API) or Fulvestrant finished formulations upon request. The Fulvestrant suppliers may include Fulvestrant API manufacturers, exporters, distributors and traders.
click here to find a list of Fulvestrant 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 Fulvestrant Drug Master File in Japan (Fulvestrant JDMF) empowers Fulvestrant 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 Fulvestrant JDMF during the approval evaluation for pharmaceutical products. At the time of Fulvestrant 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 Fulvestrant suppliers with JDMF on PharmaCompass.
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