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
A Paromomycin Sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Paromomycin Sulfate, including repackagers and relabelers. The FDA regulates Paromomycin Sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Paromomycin Sulfate 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 Paromomycin Sulfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Paromomycin Sulfate supplier is an individual or a company that provides Paromomycin Sulfate active pharmaceutical ingredient (API) or Paromomycin Sulfate finished formulations upon request. The Paromomycin Sulfate suppliers may include Paromomycin Sulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Paromomycin Sulfate 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 Paromomycin Sulfate Drug Master File in Japan (Paromomycin Sulfate JDMF) empowers Paromomycin Sulfate 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 Paromomycin Sulfate JDMF during the approval evaluation for pharmaceutical products. At the time of Paromomycin Sulfate 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 Paromomycin Sulfate suppliers with JDMF on PharmaCompass.
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