01 1Jiaxing Hengjie Biopharmaceutical Co. , Ltd.
02 1Maruha Nichiro Co., Ltd.
03 1Seikagaku Corporation
01 2Outsiders regulations sodium chondroitin sulfate
02 1Sodium chondroitin sulfate
01 1China
02 1Japan
03 1U.S.A
Registration Number : 226MF10112
Registrant's Address : No. 20 Tongyi Road, Xingfeng Town, Jiaxing, Zhejiang, China
Initial Date of Registration : 2014-05-29
Latest Date of Registration : 2014-05-29
Non-prescription sodium chondroitin sulfate
Registration Number : 217MF10125
Registrant's Address : 2-20 Toyosu 3-chome, Koto-ku, Tokyo
Initial Date of Registration : 2005-05-24
Latest Date of Registration : 2010-01-07
Non-prescription sodium chondroitin sulfate
Registration Number : 217MF10106
Registrant's Address : 1-6-1 Marunouchi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-05-23
Latest Date of Registration : 2012-05-08
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PharmaCompass offers a list of Chondroitin Sulfate Sodium 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 Chondroitin Sulfate Sodium manufacturer or Chondroitin Sulfate Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Chondroitin Sulfate Sodium API Price utilized in the formulation of products. Chondroitin Sulfate Sodium API Price is not always fixed or binding as the Chondroitin Sulfate Sodium Price is obtained through a variety of data sources. The Chondroitin Sulfate Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sodium Chondroitin Sulphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Chondroitin Sulphate, including repackagers and relabelers. The FDA regulates Sodium Chondroitin Sulphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Chondroitin Sulphate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Sodium Chondroitin Sulphate supplier is an individual or a company that provides Sodium Chondroitin Sulphate active pharmaceutical ingredient (API) or Sodium Chondroitin Sulphate finished formulations upon request. The Sodium Chondroitin Sulphate suppliers may include Sodium Chondroitin Sulphate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Chondroitin Sulphate 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 Chondroitin Sulphate Drug Master File in Japan (Sodium Chondroitin Sulphate JDMF) empowers Sodium Chondroitin Sulphate 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 Chondroitin Sulphate JDMF during the approval evaluation for pharmaceutical products. At the time of Sodium Chondroitin Sulphate JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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