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