01 1Hebei Jingye Medical Technology Corp. , LTD. ,Coastal Port Pharmaceutical Branch
02 1Yamamoto Chemical Industry Co., Ltd.
01 1Japanese Pharmacopoeia Aspirin
02 1Japanese Pharmacopoeia aspirin
01 1China
02 1Japan
Japanese Pharmacopoeia Aspirin
Registration Number : 301MF10041
Registrant's Address : East of Jingyi Road, West zone, Coastal-port economic technology development zone, Ca...
Initial Date of Registration : 2019-08-09
Latest Date of Registration : 2019-08-09
Japanese Pharmacopoeia Aspirin
Registration Number : 217MF10562
Registrant's Address : 1-4 Funatsucho, Wakayama City, Wakayama Prefecture
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2007-07-17
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PharmaCompass offers a list of Aspirin 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 Aspirin manufacturer or Aspirin supplier for your needs.
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A component of St. Joseph Cold Tablets manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of component of St. Joseph Cold Tablets, including repackagers and relabelers. The FDA regulates component of St. Joseph Cold Tablets manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. component of St. Joseph Cold Tablets 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 component of St. Joseph Cold Tablets supplier is an individual or a company that provides component of St. Joseph Cold Tablets active pharmaceutical ingredient (API) or component of St. Joseph Cold Tablets finished formulations upon request. The component of St. Joseph Cold Tablets suppliers may include component of St. Joseph Cold Tablets 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 component of St. Joseph Cold Tablets Drug Master File in Japan (component of St. Joseph Cold Tablets JDMF) empowers component of St. Joseph Cold Tablets 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 component of St. Joseph Cold Tablets JDMF during the approval evaluation for pharmaceutical products. At the time of component of St. Joseph Cold Tablets 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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