01 1F. I. S. Fabrica Italiana Sintetici S. p. A.
01 1Clotrimazole
01 1Italy
Registration Number : 221MF10167
Registrant's Address : Viale Milano 26 36075 Montecchio Maggiore Vicenza, Italy
Initial Date of Registration : 2009-07-30
Latest Date of Registration : 2023-02-02
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PharmaCompass offers a list of Clotrimazole 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 Clotrimazole manufacturer or Clotrimazole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clotrimazole manufacturer or Clotrimazole supplier.
PharmaCompass also assists you with knowing the Clotrimazole API Price utilized in the formulation of products. Clotrimazole API Price is not always fixed or binding as the Clotrimazole Price is obtained through a variety of data sources. The Clotrimazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Canesten Combi-Pak 3-Day Therapy manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Canesten Combi-Pak 3-Day Therapy, including repackagers and relabelers. The FDA regulates Canesten Combi-Pak 3-Day Therapy manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Canesten Combi-Pak 3-Day Therapy 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 Canesten Combi-Pak 3-Day Therapy manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Canesten Combi-Pak 3-Day Therapy supplier is an individual or a company that provides Canesten Combi-Pak 3-Day Therapy active pharmaceutical ingredient (API) or Canesten Combi-Pak 3-Day Therapy finished formulations upon request. The Canesten Combi-Pak 3-Day Therapy suppliers may include Canesten Combi-Pak 3-Day Therapy API manufacturers, exporters, distributors and traders.
click here to find a list of Canesten Combi-Pak 3-Day Therapy 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 Canesten Combi-Pak 3-Day Therapy Drug Master File in Japan (Canesten Combi-Pak 3-Day Therapy JDMF) empowers Canesten Combi-Pak 3-Day Therapy 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 Canesten Combi-Pak 3-Day Therapy JDMF during the approval evaluation for pharmaceutical products. At the time of Canesten Combi-Pak 3-Day Therapy 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 Canesten Combi-Pak 3-Day Therapy suppliers with JDMF on PharmaCompass.
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