Registration Number : 301MF10021
Registrant's Address : 6-8, Fructo(´)s Gelabert 08970 Sant Joan Despi(´)(Barcelona) Spain
Initial Date of Registration : 2019-06-25
Latest Date of Registration : 2019-06-25
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PharmaCompass offers a list of Clozapine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Clozapine manufacturer or Clozapine supplier for your needs.
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A Cloment manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cloment, including repackagers and relabelers. The FDA regulates Cloment manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cloment 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 Cloment manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Cloment supplier is an individual or a company that provides Cloment active pharmaceutical ingredient (API) or Cloment finished formulations upon request. The Cloment suppliers may include Cloment API manufacturers, exporters, distributors and traders.
click here to find a list of Cloment suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Cloment Drug Master File in Japan (Cloment JDMF) empowers Cloment 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 Cloment JDMF during the approval evaluation for pharmaceutical products. At the time of Cloment 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 Cloment suppliers with JDMF on PharmaCompass.
