01 Nippon Chemical Co., Ltd. (1)
02 S. C. PUROLITE S. R. L. (4)
01 Japanese Pharmacopoeia polystyrene sulfonic acid calcium (1)
02 Sodium polystyrene sulfonate (1)
03 Sodium polystyrene sulfonate (NS) (1)
04 Sodium polystyrene sulfonate (PUROLITE) (1)
05 Sodium polystyrene sulfonate (Purolite) (1)
01 Japan (1)
02 United Kingdom (4)
46
PharmaCompass offers a list of Sodium Polystyrene Sulfonate 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 Sodium Polystyrene Sulfonate manufacturer or Sodium Polystyrene Sulfonate supplier for your needs.
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PharmaCompass also assists you with knowing the Sodium Polystyrene Sulfonate API Price utilized in the formulation of products. Sodium Polystyrene Sulfonate API Price is not always fixed or binding as the Sodium Polystyrene Sulfonate Price is obtained through a variety of data sources. The Sodium Polystyrene Sulfonate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MolPort-001-786-409 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-786-409, including repackagers and relabelers. The FDA regulates MolPort-001-786-409 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-786-409 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 MolPort-001-786-409 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A MolPort-001-786-409 supplier is an individual or a company that provides MolPort-001-786-409 active pharmaceutical ingredient (API) or MolPort-001-786-409 finished formulations upon request. The MolPort-001-786-409 suppliers may include MolPort-001-786-409 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-001-786-409 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 MolPort-001-786-409 Drug Master File in Japan (MolPort-001-786-409 JDMF) empowers MolPort-001-786-409 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 MolPort-001-786-409 JDMF during the approval evaluation for pharmaceutical products. At the time of MolPort-001-786-409 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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