01 1Sekisui Medical Co., Ltd.
01 1Indigo carmine
01 1Japan
Registration Number : 217MF10769
Registrant's Address : 2-1-3 Nihonbashi, Chuo-ku, Tokyo
Initial Date of Registration : 2005-10-20
Latest Date of Registration : 2009-07-09
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PharmaCompass offers a list of Indigo Carmine 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 Indigo Carmine manufacturer or Indigo Carmine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Indigo Carmine manufacturer or Indigo Carmine supplier.
PharmaCompass also assists you with knowing the Indigo Carmine API Price utilized in the formulation of products. Indigo Carmine API Price is not always fixed or binding as the Indigo Carmine Price is obtained through a variety of data sources. The Indigo Carmine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A indigo manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of indigo, including repackagers and relabelers. The FDA regulates indigo manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. indigo 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 indigo manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A indigo supplier is an individual or a company that provides indigo active pharmaceutical ingredient (API) or indigo finished formulations upon request. The indigo suppliers may include indigo API manufacturers, exporters, distributors and traders.
click here to find a list of indigo 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 indigo Drug Master File in Japan (indigo JDMF) empowers indigo 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 indigo JDMF during the approval evaluation for pharmaceutical products. At the time of indigo 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 indigo suppliers with JDMF on PharmaCompass.
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