01 1Olon S. p. A.
01 1Paromomycin sulfate salt
01 1Italy
Registration Number : 223MF10174
Registrant's Address : Strada Rivoltana Km 6/7 20053 Rodano Milano Italy
Initial Date of Registration : 2011-12-27
Latest Date of Registration : 2012-11-28
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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 Aminosidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aminosidine, including repackagers and relabelers. The FDA regulates Aminosidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aminosidine 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 Aminosidine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aminosidine supplier is an individual or a company that provides Aminosidine active pharmaceutical ingredient (API) or Aminosidine finished formulations upon request. The Aminosidine suppliers may include Aminosidine API manufacturers, exporters, distributors and traders.
click here to find a list of Aminosidine 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 Aminosidine Drug Master File in Japan (Aminosidine JDMF) empowers Aminosidine 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 Aminosidine JDMF during the approval evaluation for pharmaceutical products. At the time of Aminosidine 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 Aminosidine suppliers with JDMF on PharmaCompass.
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