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