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