01 1Sekisui Medical Co., Ltd.
01 1Phenolsulfonphthalein
01 1Japan
Registration Number : 217MF10776
Registrant's Address : 2-1-3 Nihonbashi, Chuo-ku, Tokyo
Initial Date of Registration : 2005-10-20
Latest Date of Registration : 2009-12-15
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PharmaCompass offers a list of Phenol Red 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 Phenol Red manufacturer or Phenol Red supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Phenol Red manufacturer or Phenol Red supplier.
PharmaCompass also assists you with knowing the Phenol Red API Price utilized in the formulation of products. Phenol Red API Price is not always fixed or binding as the Phenol Red Price is obtained through a variety of data sources. The Phenol Red Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A PSP manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PSP, including repackagers and relabelers. The FDA regulates PSP manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PSP 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 PSP manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A PSP supplier is an individual or a company that provides PSP active pharmaceutical ingredient (API) or PSP finished formulations upon request. The PSP suppliers may include PSP API manufacturers, exporters, distributors and traders.
click here to find a list of PSP 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 PSP Drug Master File in Japan (PSP JDMF) empowers PSP 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 PSP JDMF during the approval evaluation for pharmaceutical products. At the time of PSP 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 PSP suppliers with JDMF on PharmaCompass.
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