01 2Oryza Oil & Fat Chemical Co., Ltd.
01 2Japanese Pharmacopoeia Acrinol
01 2Japan
Acrinol, Japanese Pharmacopoeia
Registration Number : 224MF10045
Registrant's Address : 1 Numata, Kitakata, Kitakata-cho, Ichinomiya City, Aichi Prefecture
Initial Date of Registration : 2012-02-28
Latest Date of Registration : 2012-02-28
Acrinol, Japanese Pharmacopoeia
Registration Number : 218MF10807
Registrant's Address : 1 Numata, Kitakata, Kitakata-cho, Ichinomiya City, Aichi Prefecture
Initial Date of Registration : 2006-10-06
Latest Date of Registration : 2010-11-29
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PharmaCompass offers a list of Ethacridine Lactate 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 Ethacridine Lactate manufacturer or Ethacridine Lactate supplier for your needs.
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A Neo Chinosol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neo Chinosol, including repackagers and relabelers. The FDA regulates Neo Chinosol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neo Chinosol API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Neo Chinosol supplier is an individual or a company that provides Neo Chinosol active pharmaceutical ingredient (API) or Neo Chinosol finished formulations upon request. The Neo Chinosol suppliers may include Neo Chinosol API manufacturers, exporters, distributors and traders.
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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 Neo Chinosol Drug Master File in Japan (Neo Chinosol JDMF) empowers Neo Chinosol 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 Neo Chinosol JDMF during the approval evaluation for pharmaceutical products. At the time of Neo Chinosol JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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