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
A Dextran 40 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dextran 40, including repackagers and relabelers. The FDA regulates Dextran 40 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dextran 40 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 40 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dextran 40 supplier is an individual or a company that provides Dextran 40 active pharmaceutical ingredient (API) or Dextran 40 finished formulations upon request. The Dextran 40 suppliers may include Dextran 40 API manufacturers, exporters, distributors and traders.
click here to find a list of Dextran 40 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 40 Drug Master File in Japan (Dextran 40 JDMF) empowers Dextran 40 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 40 JDMF during the approval evaluation for pharmaceutical products. At the time of Dextran 40 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 40 suppliers with JDMF on PharmaCompass.
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