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 Gino-Lotremine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gino-Lotremine, including repackagers and relabelers. The FDA regulates Gino-Lotremine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gino-Lotremine 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 Gino-Lotremine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Gino-Lotremine supplier is an individual or a company that provides Gino-Lotremine active pharmaceutical ingredient (API) or Gino-Lotremine finished formulations upon request. The Gino-Lotremine suppliers may include Gino-Lotremine API manufacturers, exporters, distributors and traders.
click here to find a list of Gino-Lotremine 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 Gino-Lotremine Drug Master File in Japan (Gino-Lotremine JDMF) empowers Gino-Lotremine 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 Gino-Lotremine JDMF during the approval evaluation for pharmaceutical products. At the time of Gino-Lotremine 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 Gino-Lotremine suppliers with JDMF on PharmaCompass.
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