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01 Kongo Chemical Co., Ltd. (1)
01 Nitric acid Bisuchiamin (production only) (1)
01 Japan (1)
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PharmaCompass offers a list of Nitric Acid 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 Nitric Acid manufacturer or Nitric Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nitric Acid manufacturer or Nitric Acid supplier.
PharmaCompass also assists you with knowing the Nitric Acid API Price utilized in the formulation of products. Nitric Acid API Price is not always fixed or binding as the Nitric Acid Price is obtained through a variety of data sources. The Nitric Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 07006_RIEDEL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 07006_RIEDEL, including repackagers and relabelers. The FDA regulates 07006_RIEDEL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 07006_RIEDEL 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 07006_RIEDEL manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 07006_RIEDEL supplier is an individual or a company that provides 07006_RIEDEL active pharmaceutical ingredient (API) or 07006_RIEDEL finished formulations upon request. The 07006_RIEDEL suppliers may include 07006_RIEDEL API manufacturers, exporters, distributors and traders.
click here to find a list of 07006_RIEDEL 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 07006_RIEDEL Drug Master File in Japan (07006_RIEDEL JDMF) empowers 07006_RIEDEL 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 07006_RIEDEL JDMF during the approval evaluation for pharmaceutical products. At the time of 07006_RIEDEL 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 07006_RIEDEL suppliers with JDMF on PharmaCompass.
We have 1 companies offering 07006_RIEDEL
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