01 1Tomita Pharmaceutical Co., Ltd.
01 1Pharmaceutical dried sodium sulfate 60SH
01 1Japan
Dry Sodium Sulfate 60SH for Pharmaceutical Use
Registration Number : 228MF10107
Registrant's Address : Tokushima Prefecture Naruto City Setocho Myojin Maruyama 85-1
Initial Date of Registration : 2016-06-06
Latest Date of Registration : 2016-06-06
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PharmaCompass offers a list of Sodium Sulfate 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 Sulfate manufacturer or Sodium Sulfate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Sulfate manufacturer or Sodium Sulfate supplier.
PharmaCompass also assists you with knowing the Sodium Sulfate API Price utilized in the formulation of products. Sodium Sulfate API Price is not always fixed or binding as the Sodium Sulfate Price is obtained through a variety of data sources. The Sodium Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Na2SO4 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Na2SO4, including repackagers and relabelers. The FDA regulates Na2SO4 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Na2SO4 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 Na2SO4 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Na2SO4 supplier is an individual or a company that provides Na2SO4 active pharmaceutical ingredient (API) or Na2SO4 finished formulations upon request. The Na2SO4 suppliers may include Na2SO4 API manufacturers, exporters, distributors and traders.
click here to find a list of Na2SO4 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 Na2SO4 Drug Master File in Japan (Na2SO4 JDMF) empowers Na2SO4 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 Na2SO4 JDMF during the approval evaluation for pharmaceutical products. At the time of Na2SO4 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 Na2SO4 suppliers with JDMF on PharmaCompass.
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