01 1Jiaxing Hengjie Biopharmaceutical Co. , Ltd.
02 1Maruha Nichiro Co., Ltd.
03 2Seikagaku Corporation
01 1For a sodium chondroitin sulfate "biochemical" injection
02 2Outsiders regulations sodium chondroitin sulfate
03 1Sodium chondroitin sulfate
01 1China
02 2Japan
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
Sodium chondroitin sulfate for extra-mural use
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
Sodium chondroitin sulfate "Seikagaku" for injection
Registration Number : 217MF10107
Registrant's Address : 1-6-1 Marunouchi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-05-23
Latest Date of Registration : 2012-05-08
Sodium chondroitin sulfate for extra-mural use
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 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 manufacturer or Chondroitin Sulfate supplier for your needs.
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PharmaCompass also assists you with knowing the Chondroitin Sulfate API Price utilized in the formulation of products. Chondroitin Sulfate API Price is not always fixed or binding as the Chondroitin Sulfate Price is obtained through a variety of data sources. The Chondroitin Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Chondroitin Sulphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chondroitin Sulphate, including repackagers and relabelers. The FDA regulates Chondroitin Sulphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 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 Chondroitin Sulphate supplier is an individual or a company that provides Chondroitin Sulphate active pharmaceutical ingredient (API) or Chondroitin Sulphate finished formulations upon request. The Chondroitin Sulphate suppliers may include Chondroitin Sulphate API manufacturers, exporters, distributors and traders.
click here to find a list of 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 Chondroitin Sulphate Drug Master File in Japan (Chondroitin Sulphate JDMF) empowers 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 Chondroitin Sulphate JDMF during the approval evaluation for pharmaceutical products. At the time of 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.
click here to find a list of Chondroitin Sulphate suppliers with JDMF on PharmaCompass.
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