01 1F. I. S. Fabrica Italiana Sintetici S. p. A.
01 1Clomiphene citrate
01 1Italy
Registration Number : 226MF10082
Registrant's Address : Viale Milano 26 36075 Montecchio Maggiore Vicenza, Italy
Initial Date of Registration : 2014-05-02
Latest Date of Registration : 2017-03-30
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PharmaCompass offers a list of Clomiphene Citrate 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 Clomiphene Citrate manufacturer or Clomiphene Citrate supplier for your needs.
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PharmaCompass also assists you with knowing the Clomiphene Citrate API Price utilized in the formulation of products. Clomiphene Citrate API Price is not always fixed or binding as the Clomiphene Citrate Price is obtained through a variety of data sources. The Clomiphene Citrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Clomid;Serophene;Milophene manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clomid;Serophene;Milophene, including repackagers and relabelers. The FDA regulates Clomid;Serophene;Milophene manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clomid;Serophene;Milophene 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 Clomid;Serophene;Milophene supplier is an individual or a company that provides Clomid;Serophene;Milophene active pharmaceutical ingredient (API) or Clomid;Serophene;Milophene finished formulations upon request. The Clomid;Serophene;Milophene suppliers may include Clomid;Serophene;Milophene API manufacturers, exporters, distributors and traders.
click here to find a list of Clomid;Serophene;Milophene 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 Clomid;Serophene;Milophene Drug Master File in Japan (Clomid;Serophene;Milophene JDMF) empowers Clomid;Serophene;Milophene 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 Clomid;Serophene;Milophene JDMF during the approval evaluation for pharmaceutical products. At the time of Clomid;Serophene;Milophene 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 Clomid;Serophene;Milophene suppliers with JDMF on PharmaCompass.
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