01 1Asahi Kasei Finechem Co., Ltd.
01 1Omidenepagu isopropyl
01 1Japan
Registration Number : 229MF10105
Registrant's Address : 3-3-23 Nakanoshima, Kita-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2017-06-21
Latest Date of Registration : 2018-07-26
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PharmaCompass offers a list of Omidenepag Isopropyl 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 Omidenepag Isopropyl manufacturer or Omidenepag Isopropyl supplier for your needs.
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PharmaCompass also assists you with knowing the Omidenepag Isopropyl API Price utilized in the formulation of products. Omidenepag Isopropyl API Price is not always fixed or binding as the Omidenepag Isopropyl Price is obtained through a variety of data sources. The Omidenepag Isopropyl Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Omidenepag Isopropyl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Omidenepag Isopropyl, including repackagers and relabelers. The FDA regulates Omidenepag Isopropyl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Omidenepag Isopropyl 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 Omidenepag Isopropyl supplier is an individual or a company that provides Omidenepag Isopropyl active pharmaceutical ingredient (API) or Omidenepag Isopropyl finished formulations upon request. The Omidenepag Isopropyl suppliers may include Omidenepag Isopropyl API manufacturers, exporters, distributors and traders.
click here to find a list of Omidenepag Isopropyl 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 Omidenepag Isopropyl Drug Master File in Japan (Omidenepag Isopropyl JDMF) empowers Omidenepag Isopropyl 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 Omidenepag Isopropyl JDMF during the approval evaluation for pharmaceutical products. At the time of Omidenepag Isopropyl 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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