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01 Olon S. p. A. (1)
01 Paromomycin sulfate salt (1)
01 Italy (1)
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PharmaCompass offers a list of Paromomycin 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 Paromomycin Sulfate manufacturer or Paromomycin Sulfate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Paromomycin Sulfate manufacturer or Paromomycin Sulfate supplier.
PharmaCompass also assists you with knowing the Paromomycin Sulfate API Price utilized in the formulation of products. Paromomycin Sulfate API Price is not always fixed or binding as the Paromomycin Sulfate Price is obtained through a variety of data sources. The Paromomycin Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 1263-89-4 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 1263-89-4, including repackagers and relabelers. The FDA regulates 1263-89-4 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 1263-89-4 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 1263-89-4 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 1263-89-4 supplier is an individual or a company that provides 1263-89-4 active pharmaceutical ingredient (API) or 1263-89-4 finished formulations upon request. The 1263-89-4 suppliers may include 1263-89-4 API manufacturers, exporters, distributors and traders.
click here to find a list of 1263-89-4 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 1263-89-4 Drug Master File in Japan (1263-89-4 JDMF) empowers 1263-89-4 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 1263-89-4 JDMF during the approval evaluation for pharmaceutical products. At the time of 1263-89-4 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 1263-89-4 suppliers with JDMF on PharmaCompass.
