01 3Meito Sangyo Co., Ltd.
01 1Dextran 40
02 1Dextran sulfate sodium sulfur 18
03 1Dextran sulfate sodium sulfur 5
01 3Japan
Dextran sulfate sodium sulfur 5
Registration Number : 218MF10831
Registrant's Address : 2-41 Sasazukacho, Nishi-ku, Nagoya
Initial Date of Registration : 2006-10-20
Latest Date of Registration : 2006-10-20
Dextran sulfate sodium sulfur-18
Registration Number : 218MF10826
Registrant's Address : 2-41 Sasazukacho, Nishi-ku, Nagoya
Initial Date of Registration : 2006-10-20
Latest Date of Registration : 2006-10-20
Registration Number : 217MF11169
Registrant's Address : 2-41 Sasazukacho, Nishi-ku, Nagoya City, Aichi Prefecture
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2018-10-01
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PharmaCompass offers a list of Dextrans 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 Dextrans manufacturer or Dextrans supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dextrans manufacturer or Dextrans supplier.
PharmaCompass also assists you with knowing the Dextrans API Price utilized in the formulation of products. Dextrans API Price is not always fixed or binding as the Dextrans Price is obtained through a variety of data sources. The Dextrans Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dextran 70 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dextran 70, including repackagers and relabelers. The FDA regulates Dextran 70 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dextran 70 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 Dextran 70 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dextran 70 supplier is an individual or a company that provides Dextran 70 active pharmaceutical ingredient (API) or Dextran 70 finished formulations upon request. The Dextran 70 suppliers may include Dextran 70 API manufacturers, exporters, distributors and traders.
click here to find a list of Dextran 70 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 Dextran 70 Drug Master File in Japan (Dextran 70 JDMF) empowers Dextran 70 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 Dextran 70 JDMF during the approval evaluation for pharmaceutical products. At the time of Dextran 70 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 Dextran 70 suppliers with JDMF on PharmaCompass.
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